A General and Practical Approach for the Synthesis of 1,2,4‐Trioxanes Catalyzed by Silica‐Ferric Chloride
An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefit...
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Published in | Advanced synthesis & catalysis Vol. 359; no. 20; pp. 3618 - 3625 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
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Wiley
25.10.2017
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Abstract | An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefits of operational simplicity, high yields and potential large‐scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity. |
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AbstractList | An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefits of operational simplicity, high yields and potential large‐scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity. An efficient and practical method has been developed for the facile synthesis of 1,2,4-trioxanes by the condensation of beta-hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica-supported ferric chloride (FeCl3/SiO2) at room temperature. The method has the benefits of operational simplicity, high yields and potential large-scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity. An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl compounds in the presence of a catalytic amount of silica‐supported ferric chloride (FeCl 3 /SiO 2 ) at room temperature. The method has the benefits of operational simplicity, high yields and potential large‐scale application. Moreover, the catalyst can be readily recovered by simple filtration and reused up to five times while almost maintaining its catalytic activity. magnified image |
Author | Han, Yi Zhang, Mo Niu, Jia‐Liang Zhang, Zhan‐Hui |
Author_xml | – sequence: 1 givenname: Mo surname: Zhang fullname: Zhang, Mo organization: Hebei Normal University – sequence: 2 givenname: Yi surname: Han fullname: Han, Yi organization: Hebei Normal University – sequence: 3 givenname: Jia‐Liang surname: Niu fullname: Niu, Jia‐Liang organization: Hebei Normal University – sequence: 4 givenname: Zhan‐Hui surname: Zhang fullname: Zhang, Zhan‐Hui email: zhanhui@mail.nankai.edu.cn organization: Hebei Normal University |
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Cites_doi | 10.1016/j.catcom.2016.09.028 10.1039/c3nj01368e 10.1039/C5GC00381D 10.1002/ejoc.201500919 10.1016/j.cclet.2015.01.035 10.1021/jm9002523 10.1016/j.tetlet.2016.12.002 10.1016/0040-4039(91)80487-Q 10.1139/v99-001 10.1021/jm400004u 10.1002/anie.200701397 10.1016/j.catcom.2006.02.026 10.1021/acssuschemeng.7b01102 10.1021/acs.joc.6b02091 10.1016/j.tet.2014.02.017 10.1002/adsc.201600357 10.1021/acs.joc.5b00533 10.1016/j.mcat.2016.12.001 10.1016/j.bmcl.2005.07.013 10.1246/cl.140624 10.1021/jm0610043 10.1055/s-0030-1261225 10.1007/s00706-009-0204-9 10.1080/00397910802412842 10.1016/S1872-2067(15)60829-4 10.1002/cctc.201402415 10.1021/ol0492142 10.1016/j.catcom.2016.02.004 10.1002/adsc.201500335 10.1007/s00706-014-1275-9 10.1002/adsc.201600565 10.1002/hlca.19930760804 10.3987/COM-97-S51 10.1016/j.tet.2013.06.049 10.1002/cplu.201600611 10.1039/c3ob27239g 10.1016/j.bmc.2004.08.042 10.1021/acssuschemeng.5b01183 10.1021/jm100678p 10.1002/adsc.201600759 10.1002/adsc.201100561 10.3762/bjoc.12.162 10.1002/hlca.19970800813 10.1002/cmdc.201402553 10.1021/jm301323k 10.1021/ml300188t 10.1016/j.apcata.2014.06.006 10.1080/00304948.2012.697708 10.1002/chem.201300076 10.1002/adsc.201600577 10.1055/s-0035-1561599 10.2174/1385272820666161020150646 10.1039/c2ob25376c 10.1016/j.bmcl.2010.06.045 10.1002/adsc.201300551 10.1002/ejoc.201500326 10.1016/j.ccr.2015.01.001 10.1039/C6RA19579B 10.1351/pac200577061059 10.1016/j.tetlet.2016.08.099 10.1016/j.bmcl.2007.05.055 10.2174/157017806775789903 10.1021/cr500425u 10.1021/ol026916n 10.1002/adsc.201600503 10.1002/ange.200701397 10.1016/j.bmcl.2004.11.043 10.1080/00397911.2016.1167910 10.1055/s-2005-872103 10.1039/c5gc00381d 10.1055/s-0032-1317958 10.1055/s-0028-1083147 10.1039/c6ra19579b |
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Keywords | CONVENIENT SYNTHESIS 1,2,4-trioxanes ONE-POT SYNTHESIS MAGNETICALLY SEPARABLE CATALYST PROMOTED ONE-POT carbonyl compounds beta-hydroperoxy alcohols silica-supported iron(III) chloride SUPPORTED MOLYBDENUM SPIRO 1,2,4-TRIOXANES DIASTEREOSELECTIVE FORMATION 4-COMPONENT SYNTHESIS RECYCLABLE CATALYST ANTIMALARIAL 1,2,4-TRIOXANES |
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References | 1997; 80 2017; 5 2010; 53 2015; 36 2014; 70 2013; 4 2013; 69 2017; 82 2013; 24 2015; 146 2017; 88 1997; 46 2004; 6 2015; 80 2012; 55 2017; 433 2012; 10 2016; 78 2013; 19 2010; 20 2009; 52 2013; 11 2013; 56 1993; 76 2013; 355 2016; 358 2016; 81 2014; 482 2014; 6 2005; 77 2016; 46 2007; 17 2015; 17 2009; 21 2011 1991; 32 2015; 288 2017; 21 2015; 10 2006; 7 2008 2002; 4 2006; 3 2005 2007; 50 2016; 57 2016; 12 2014; 43 2016; 4 2015; 26 2016; 6 2012; 354 2015; 115 2017; 58 2015; 357 2004; 12 2014; 38 1999; 77 2015 2009; 140 2007 2007; 119 46 2005; 15 2016; 27 2012; 44 2009; 39 e_1_2_6_51_1 e_1_2_6_53_2 e_1_2_6_74_2 e_1_2_6_32_1 e_1_2_6_30_1 e_1_2_6_72_1 e_1_2_6_19_1 e_1_2_6_13_2 e_1_2_6_34_2 e_1_2_6_59_2 e_1_2_6_11_2 e_1_2_6_17_1 e_1_2_6_38_2 e_1_2_6_55_2 e_1_2_6_76_2 e_1_2_6_15_1 e_1_2_6_57_2 e_1_2_6_78_2 e_1_2_6_62_1 e_1_2_6_64_1 e_1_2_6_81_1 e_1_2_6_20_1 e_1_2_6_41_2 e_1_2_6_60_2 Ravi M. (e_1_2_6_29_2) 2013; 24 e_1_2_6_7_2 e_1_2_6_9_3 e_1_2_6_9_2 e_1_2_6_3_2 e_1_2_6_5_2 e_1_2_6_24_2 e_1_2_6_47_2 e_1_2_6_49_2 e_1_2_6_28_2 e_1_2_6_43_2 e_1_2_6_66_1 e_1_2_6_26_2 e_1_2_6_45_2 e_1_2_6_68_1 e_1_2_6_50_2 e_1_2_6_73_2 e_1_2_6_52_2 e_1_2_6_75_2 e_1_2_6_31_1 e_1_2_6_71_2 e_1_2_6_12_2 e_1_2_6_35_2 e_1_2_6_58_2 e_1_2_6_10_2 e_1_2_6_33_2 e_1_2_6_54_2 e_1_2_6_77_2 e_1_2_6_18_1 Bartoschek A. (e_1_2_6_36_2) 2005 e_1_2_6_39_1 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_56_2 e_1_2_6_79_2 e_1_2_6_16_1 e_1_2_6_63_1 e_1_2_6_42_2 e_1_2_6_65_1 e_1_2_6_21_1 e_1_2_6_80_2 e_1_2_6_40_2 e_1_2_6_61_1 e_1_2_6_8_2 e_1_2_6_4_2 Kumar L. (e_1_2_6_22_2) 2009; 21 e_1_2_6_6_1 Liu Y. H. (e_1_2_6_70_2) 2008 e_1_2_6_25_1 e_1_2_6_23_2 e_1_2_6_48_2 e_1_2_6_2_1 e_1_2_6_27_2 e_1_2_6_44_2 e_1_2_6_67_1 e_1_2_6_69_1 e_1_2_6_46_2 Gawande, MB (WOS:000352252900006) 2015; 288 Liu, YH (WOS:000300448400024) 2012; 354 Pandit, RP (WOS:000390408200010) 2016; 358 Singh, C (WOS:000243889100013) 2007; 50 Mir, BA (WOS:000390407300017) 2016; 358 Griesbeck, AG (WOS:000226935700020) 2005; 15 Maurya, R (WOS:000315182000009) 2013; 4 Sharma, RK (WOS:000371755400060) 2016; 4 Li, BL (WOS:000322098000010) 2013; 69 Kadam, RG (WOS:000398034000019) 2017; 82 Singh, C (WOS:000231936700016) 2005; 15 An, YS (WOS:000347161300017) 2015; 146 Zhou, SH (WOS:000400562600013) 2017; 433 Ravi, M (WOS:000314697700008) 2013; 24 Habibi, D (WOS:000352678400020) 2015; 36 Kalhor, S (WOS:000357224900023) 2015; 26 Singh, C (WOS:000279866300036) 2010; 20 Zhang, M (WOS:000373418700006) 2016; 78 JEFFORD, CW (WOS:A1993MN64900003) 1993; 76 Mischne, MP (WOS:000079823200010) 1999; 77 Yao, N (WOS:000394169000011) 2017; 21 Murakami, R (WOS:000375004700012) 2016; 27 Griesbeck, A. G. (000413673600025.13) 2007; 119 Wang, XF (WOS:000317032200031) 2013; 56 Chari, MA (WOS:000241320000010) 2006; 7 Singh, C (WOS:000248462300001) 2007; 17 Bauer, I (WOS:000354906800005) 2015; 115 Zhang, M (WOS:000405139100063) 2017; 5 Klapotke, TM (WOS:000362747900013) 2015; 2015 Singh, C (WOS:000225050500002) 2004; 12 Bartoschek, A (WOS:000231847000026) 2005 Estevao, MS (WOS:000392896200008) 2017; 58 Griesbeck, AG (WOS:000236167900019) 2006; 3 (000413673600025.1) 2007; 46 O'Neill, PM (WOS:000223581900005) 2004; 6 Sawama, Y (WOS:000390264700002) 2016; 358 Tindall, DJ (WOS:000382969500008) 2016; 358 Kumar, M (WOS:000362527100014) 2015; 357 Zhang, ZH (WOS:000272376400012) 2009; 140 Donatoni, MC (WOS:000335873500003) 2014; 70 Zhang, M (WOS:000389330700014) 2016; 6 Griesbeck, AG (WOS:000358085100011) 2015; 2015 Jefford, CW (WOS:000071175600012) 1997; 80 JEFFORD, CW (WOS:A1991GU56900027) 1991; 32 Singh, C (WOS:000312227300030) 2012; 55 Liu, YH (WOS:000262859200002) 2009; 39 Brautigam, M (WOS:000351773300007) 2015; 10 Jefford, CW (WOS:000071491900064) 1997; 46 Liu, YH (WOS:000260777300018) 2008 Li, BL (WOS:000336821000038) 2014; 38 Bharate, SB (WOS:000305191000020) 2012; 10 Neto, JSS (WOS:000390408200009) 2016; 358 Sharma, RK (WOS:000355925900002) 2015; 17 Ghosh, P (WOS:000377815800004) 2016; 46 Kumar, L (WOS:000264759200030) 2009; 21 Zhang, YK (WOS:000307059200002) 2012; 44 Griesbeck, AG (WOS:000295158200031) 2011 Lu, J (WOS:000342795000017) 2014; 6 Zhang, M (WOS:000389117500010) 2017; 88 Griesbeck, AG (WOS:000230007100012) 2005; 77 Singh, C (WOS:000283703000008) 2010; 53 Li, PH (WOS:000328149300029) 2013; 355 Ramachandran, G (WOS:000343272600036) 2014; 43 Naidu, PS (WOS:000356845800040) 2015; 80 Terent'ev, AO (WOS:000316803900010) 2013; 11 Zhao, XN (WOS:000340306500031) 2014; 482 Griesbeck, AG (WOS:000266296200033) 2009; 52 Hao, HD (WOS:000319417500038) 2013; 19 Yaremenko, IA (WOS:000381258800001) 2016; 12 Samanta, S (WOS:000386187500063) 2016; 81 Griesbeck, AG (WOS:000179430600003) 2002; 4 Majumdar, S (WOS:000384873300021) 2016; 57 |
References_xml | – start-page: 3314 year: 2008 end-page: 3318 publication-title: Synthesis – volume: 354 start-page: 441 year: 2012 end-page: 447 publication-title: Adv. Synth. Catal. – volume: 358 start-page: 3586 year: 2016 end-page: 3599 publication-title: Adv. Synth. Catal. – volume: 43 start-page: 1631 year: 2014 end-page: 1633 publication-title: Chem. Lett. – volume: 433 start-page: 91 year: 2017 end-page: 99 publication-title: Mol. Catal. – volume: 4 start-page: 1123 year: 2016 end-page: 1130 publication-title: ACS Sustainable Chem. Eng. – volume: 77 start-page: 237 year: 1999 end-page: 242 publication-title: Can. J. Chem. – volume: 80 start-page: 6381 year: 2015 end-page: 6390 publication-title: J. Org. Chem. – volume: 12 start-page: 5745 year: 2004 end-page: 5752 publication-title: Bioorg. Med. Chem. – volume: 38 start-page: 2435 year: 2014 end-page: 2442 publication-title: New J. Chem. – volume: 88 start-page: 39 year: 2017 end-page: 44 publication-title: Catal. Commun. – volume: 5 start-page: 6175 year: 2017 end-page: 6182 publication-title: ACS Sustainable Chem. Eng. – volume: 44 start-page: 340 year: 2012 end-page: 374 publication-title: Org. Prep. Proced. Int. – volume: 17 start-page: 4097 year: 2007 end-page: 4101 publication-title: Bioorg. Med. Chem. Lett. – volume: 27 start-page: 1187 year: 2016 end-page: 1192 publication-title: Synlett – volume: 355 start-page: 2952 year: 2013 end-page: 2959 publication-title: Adv. Synth. Catal. – volume: 6 start-page: 106160 year: 2016 end-page: 106170 publication-title: RSC Adv. – volume: 26 start-page: 735 year: 2015 end-page: 738 publication-title: Chin. Chem. Lett. – volume: 82 start-page: 467 year: 2017 end-page: 473 publication-title: ChemPlusChem – volume: 52 start-page: 3420 year: 2009 end-page: 3423 publication-title: J. Med. Chem. – volume: 80 start-page: 2440 year: 1997 end-page: 2455 publication-title: Helv. Chim. Acta – volume: 70 start-page: 3231 year: 2014 end-page: 323 publication-title: Tetrahedron – volume: 24 start-page: 173 year: 2013 end-page: 176 publication-title: Synlett – volume: 358 start-page: 3471 year: 2016 end-page: 3476 publication-title: Adv. Synth. Catal. – volume: 53 start-page: 7587 year: 2010 end-page: 7598 publication-title: J. Med. Chem. – volume: 358 start-page: 3683 year: 2016 end-page: 3687 publication-title: Adv. Synth. Catal. – volume: 358 start-page: 2398 year: 2016 end-page: 2403 publication-title: Adv. Synth. Catal. – volume: 46 start-page: 685 year: 2016 end-page: 691 publication-title: Synth. Commun. – volume: 55 start-page: 10662 year: 2012 end-page: 10673 publication-title: J. Med. Chem. – volume: 32 start-page: 7243 year: 1991 end-page: 7246 publication-title: Tetrahedron Lett. – volume: 119 46 start-page: 9040 8883 year: 2007 2007 end-page: 9043 8886 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 146 start-page: 165 year: 2015 end-page: 172 publication-title: Monatsh. Chem. – volume: 39 start-page: 580 year: 2009 end-page: 589 publication-title: Synth. Commun. – volume: 482 start-page: 258 year: 2014 end-page: 265 publication-title: Appl. Catal. A: Gen. – volume: 78 start-page: 26 year: 2016 end-page: 32 publication-title: Catal. Commun. – volume: 21 start-page: 3540 year: 2009 end-page: 3546 publication-title: Asian J. Chem. – volume: 6 start-page: 2854 year: 2014 end-page: 2859 publication-title: ChemCatChem – volume: 357 start-page: 2862 year: 2015 end-page: 286 publication-title: Adv. Synth. Catal. – volume: 58 start-page: 302 year: 2017 end-page: 304 publication-title: Tetrahedron Lett. – volume: 77 start-page: 1059 year: 2005 end-page: 1074 publication-title: Pure Appl. Chem. – volume: 76 start-page: 2775 year: 1993 end-page: 2788 publication-title: Helv. Chim. Acta – volume: 69 start-page: 7011 year: 2013 end-page: 7018 publication-title: Tetrahedron – start-page: 2433 year: 2005 end-page: 2444 publication-title: Synthesis – volume: 358 start-page: 3572 year: 2016 end-page: 3585 publication-title: Adv. Synth. Catal. – volume: 15 start-page: 4484 year: 2005 end-page: 4487 publication-title: Bioorg. Med. Chem. Lett. – volume: 140 start-page: 1481 year: 2009 end-page: 1483 publication-title: Monatsh. Chem. – volume: 7 start-page: 787 year: 2006 end-page: 790 publication-title: Catal. Commun. – volume: 17 start-page: 3207 year: 2015 end-page: 3230 publication-title: Green Chem. – volume: 57 start-page: 4595 year: 2016 end-page: 4598 publication-title: Tetrahedron Lett. – volume: 4 start-page: 4193 year: 2002 end-page: 4195 publication-title: Org. Lett. – volume: 50 start-page: 521 year: 2007 end-page: 527 publication-title: J. Med. Chem. – volume: 10 start-page: 5143 year: 2012 end-page: 5150 publication-title: Org. Biomol. Chem. – start-page: 6237 year: 2015 end-page: 6242 publication-title: Eur. J. Org. Chem. – volume: 4 start-page: 165 year: 2013 end-page: 169 publication-title: ACS Med. Chem. Lett. – volume: 115 start-page: 3170 year: 2015 end-page: 3387 publication-title: Chem. Rev. – volume: 36 start-page: 620 year: 2015 end-page: 625 publication-title: Chin. J. Catal. – volume: 11 start-page: 2613 year: 2013 end-page: 2623 publication-title: Org. Biomol. Chem. – volume: 3 start-page: 247 year: 2006 end-page: 249 publication-title: Lett. Org. Chem. – volume: 288 start-page: 118 year: 2015 end-page: 143 publication-title: Coord. Chem. Rev. – volume: 20 start-page: 4459 year: 2010 end-page: 4463 publication-title: Bioorg. Med. Chem. Lett. – volume: 56 start-page: 2547 year: 2013 end-page: 2255 publication-title: J. Med. Chem. – volume: 21 start-page: 368 year: 2017 end-page: 377 publication-title: Curr. Org. Chem. – volume: 10 start-page: 629 year: 2015 end-page: 639 publication-title: ChemMedChem – start-page: 2430 year: 2011 end-page: 2432 publication-title: Synlett – volume: 15 start-page: 595 year: 2005 end-page: 597 publication-title: Bioorg. Med. Chem. Lett. – volume: 81 start-page: 10088 year: 2016 end-page: 10093 publication-title: J. Org. Chem. – volume: 46 start-page: 451 year: 1997 end-page: 462 publication-title: Heterocycles – volume: 6 start-page: 3035 year: 2004 end-page: 3038 publication-title: Org. Lett. – start-page: 4349 year: 2015 end-page: 4352 publication-title: Eur. J. Org. Chem. – volume: 12 start-page: 1647 year: 2016 end-page: 1748 publication-title: Beilstein J. Org. Chem. – volume: 19 start-page: 7605 year: 2013 end-page: 7619 publication-title: Chem. Eur. J. – volume: 24 start-page: 173 year: 2013 ident: e_1_2_6_29_2 publication-title: Synlett – ident: e_1_2_6_79_2 doi: 10.1016/j.catcom.2016.09.028 – ident: e_1_2_6_75_2 doi: 10.1039/c3nj01368e – ident: e_1_2_6_45_2 doi: 10.1039/C5GC00381D – ident: e_1_2_6_4_2 doi: 10.1002/ejoc.201500919 – ident: e_1_2_6_64_1 doi: 10.1016/j.cclet.2015.01.035 – ident: e_1_2_6_12_2 doi: 10.1021/jm9002523 – ident: e_1_2_6_49_2 doi: 10.1016/j.tetlet.2016.12.002 – ident: e_1_2_6_16_1 doi: 10.1016/0040-4039(91)80487-Q – ident: e_1_2_6_17_1 doi: 10.1139/v99-001 – ident: e_1_2_6_30_1 doi: 10.1021/jm400004u – ident: e_1_2_6_9_3 doi: 10.1002/anie.200701397 – ident: e_1_2_6_66_1 doi: 10.1016/j.catcom.2006.02.026 – ident: e_1_2_6_80_2 doi: 10.1021/acssuschemeng.7b01102 – ident: e_1_2_6_59_2 doi: 10.1021/acs.joc.6b02091 – ident: e_1_2_6_61_1 doi: 10.1016/j.tet.2014.02.017 – ident: e_1_2_6_60_2 doi: 10.1002/adsc.201600357 – ident: e_1_2_6_53_2 doi: 10.1021/acs.joc.5b00533 – ident: e_1_2_6_81_1 doi: 10.1016/j.mcat.2016.12.001 – ident: e_1_2_6_23_2 doi: 10.1016/j.bmcl.2005.07.013 – ident: e_1_2_6_62_1 doi: 10.1246/cl.140624 – ident: e_1_2_6_10_2 doi: 10.1021/jm0610043 – ident: e_1_2_6_72_1 – ident: e_1_2_6_35_2 doi: 10.1055/s-0030-1261225 – ident: e_1_2_6_40_2 doi: 10.1007/s00706-009-0204-9 – ident: e_1_2_6_41_2 doi: 10.1080/00397910802412842 – ident: e_1_2_6_69_1 – ident: e_1_2_6_67_1 doi: 10.1016/S1872-2067(15)60829-4 – start-page: 3314 year: 2008 ident: e_1_2_6_70_2 publication-title: Synthesis – ident: e_1_2_6_74_2 doi: 10.1002/cctc.201402415 – ident: e_1_2_6_28_2 doi: 10.1021/ol0492142 – ident: e_1_2_6_77_2 doi: 10.1016/j.catcom.2016.02.004 – ident: e_1_2_6_54_2 doi: 10.1002/adsc.201500335 – ident: e_1_2_6_68_1 doi: 10.1007/s00706-014-1275-9 – ident: e_1_2_6_6_1 – ident: e_1_2_6_58_2 doi: 10.1002/adsc.201600565 – ident: e_1_2_6_19_1 doi: 10.1002/hlca.19930760804 – ident: e_1_2_6_20_1 doi: 10.3987/COM-97-S51 – ident: e_1_2_6_73_2 doi: 10.1016/j.tet.2013.06.049 – ident: e_1_2_6_48_2 doi: 10.1002/cplu.201600611 – ident: e_1_2_6_3_2 doi: 10.1039/c3ob27239g – ident: e_1_2_6_7_2 doi: 10.1016/j.bmc.2004.08.042 – ident: e_1_2_6_51_1 – ident: e_1_2_6_47_2 doi: 10.1021/acssuschemeng.5b01183 – ident: e_1_2_6_13_2 doi: 10.1021/jm100678p – ident: e_1_2_6_55_2 doi: 10.1002/adsc.201600759 – ident: e_1_2_6_43_2 doi: 10.1002/adsc.201100561 – ident: e_1_2_6_5_2 doi: 10.3762/bjoc.12.162 – ident: e_1_2_6_18_1 doi: 10.1002/hlca.19970800813 – ident: e_1_2_6_38_2 doi: 10.1002/cmdc.201402553 – ident: e_1_2_6_27_2 doi: 10.1021/jm301323k – ident: e_1_2_6_14_2 doi: 10.1021/ml300188t – ident: e_1_2_6_39_1 – ident: e_1_2_6_76_2 doi: 10.1016/j.apcata.2014.06.006 – ident: e_1_2_6_15_1 doi: 10.1080/00304948.2012.697708 – ident: e_1_2_6_25_1 – volume: 21 start-page: 3540 year: 2009 ident: e_1_2_6_22_2 publication-title: Asian J. Chem. – ident: e_1_2_6_26_2 doi: 10.1002/chem.201300076 – ident: e_1_2_6_57_2 doi: 10.1002/adsc.201600577 – ident: e_1_2_6_2_1 – ident: e_1_2_6_46_2 doi: 10.1055/s-0035-1561599 – ident: e_1_2_6_50_2 doi: 10.2174/1385272820666161020150646 – ident: e_1_2_6_42_2 doi: 10.1039/c2ob25376c – ident: e_1_2_6_24_2 doi: 10.1016/j.bmcl.2010.06.045 – ident: e_1_2_6_71_2 doi: 10.1002/adsc.201300551 – ident: e_1_2_6_31_1 doi: 10.1002/ejoc.201500326 – ident: e_1_2_6_44_2 doi: 10.1016/j.ccr.2015.01.001 – ident: e_1_2_6_78_2 doi: 10.1039/C6RA19579B – ident: e_1_2_6_21_1 – ident: e_1_2_6_8_2 doi: 10.1351/pac200577061059 – ident: e_1_2_6_65_1 doi: 10.1016/j.tetlet.2016.08.099 – ident: e_1_2_6_11_2 doi: 10.1016/j.bmcl.2007.05.055 – ident: e_1_2_6_33_2 doi: 10.2174/157017806775789903 – start-page: 2433 year: 2005 ident: e_1_2_6_36_2 publication-title: Synthesis – ident: e_1_2_6_32_1 – ident: e_1_2_6_52_2 doi: 10.1021/cr500425u – ident: e_1_2_6_34_2 doi: 10.1021/ol026916n – ident: e_1_2_6_56_2 doi: 10.1002/adsc.201600503 – ident: e_1_2_6_9_2 doi: 10.1002/ange.200701397 – ident: e_1_2_6_37_2 doi: 10.1016/j.bmcl.2004.11.043 – ident: e_1_2_6_63_1 doi: 10.1080/00397911.2016.1167910 – volume: 482 start-page: 258 year: 2014 ident: WOS:000340306500031 article-title: Magnetic CoFe2O4 nanoparticle immobilized N-propyl diethylenetriamine sulfamic acid as an efficient and recyclable catalyst for the synthesis of amides via the Ritter reaction publication-title: APPLIED CATALYSIS A-GENERAL doi: 10.1016/j.apcata.2014.06.006 – volume: 46 start-page: 451 year: 1997 ident: WOS:000071491900064 article-title: The photo-oxygenation of dihydropyrans. Formation of 1,2-dioxetanes and 1,2,4-trioxanes publication-title: HETEROCYCLES – volume: 2015 start-page: 6237 year: 2015 ident: WOS:000362747900013 article-title: Energetic Organic Peroxides - Synthesis and Characterization of 1,4-Dimethyl-2,3,5,6-tetraoxabicyclo[2.2.1]heptanes publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.201500919 – start-page: 2433 year: 2005 ident: WOS:000231847000026 article-title: A family of new 1,2,4-trioxanes by photooxygenation of allylic alcohols in sensitizer-doped polymers and secondary reactions publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-2005-872103 – volume: 15 start-page: 4484 year: 2005 ident: WOS:000231936700016 article-title: New orally active spiro 1,2,4-trioxanes with high antimalarial potency publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2005.07.013 – volume: 140 start-page: 1481 year: 2009 ident: WOS:000272376400012 article-title: A facile and efficient method for synthesis of xanthone derivatives catalyzed by HBF4/SiO2 under solvent-free conditions publication-title: MONATSHEFTE FUR CHEMIE doi: 10.1007/s00706-009-0204-9 – volume: 115 start-page: 3170 year: 2015 ident: WOS:000354906800005 article-title: Iron Catalysis in Organic Synthesis publication-title: CHEMICAL REVIEWS doi: 10.1021/cr500425u – volume: 119 start-page: 9040 year: 2007 ident: 000413673600025.13 publication-title: Angew. Chem. – volume: 4 start-page: 1123 year: 2016 ident: WOS:000371755400060 article-title: Silica-Based Magnetic Manganese Nanocatalyst - Applications in the Oxidation of Organic Halides and Alcohols publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING doi: 10.1021/acssuschemeng.5b01183 – volume: 55 start-page: 10662 year: 2012 ident: WOS:000312227300030 article-title: Bile Acid-Based 1,2,4-Trioxanes: Synthesis and Antimalarial Assessment publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm301323k – volume: 358 start-page: 2398 year: 2016 ident: WOS:000382969500008 article-title: Iron-Catalyzed Cross-Coupling of 1-Alkynylcyclopropyl Tosylates and Related Substrates publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600357 – volume: 76 start-page: 2775 year: 1993 ident: WOS:A1993MN64900003 article-title: SYNTHESIS, STRUCTURE, AND ANTIMALARIAL ACTIVITY OF TRICYCLIC 1,2,4-TRIOXANES RELATED TO ARTEMISININ publication-title: HELVETICA CHIMICA ACTA – volume: 44 start-page: 340 year: 2012 ident: WOS:000307059200002 article-title: Recent Progress in the Synthesis of Antimalarial Agents publication-title: ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL doi: 10.1080/00304948.2012.697708 – volume: 80 start-page: 6381 year: 2015 ident: WOS:000356845800040 article-title: Reductive Alkylation of alpha-Keto Imines Catalyzed by PTSA/FeCl3: Synthesis of Indoles and 2,3 '-Biindoles publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.5b00533 – volume: 3 start-page: 247 year: 2006 ident: WOS:000236167900019 article-title: Synthetic approaches to polar antimalarial 1,2,4-trioxanes from C-5-aldehyde and ipsdienol publication-title: LETTERS IN ORGANIC CHEMISTRY – volume: 7 start-page: 787 year: 2006 ident: WOS:000241320000010 article-title: Silica gel/FeCl3: An efficient and recyclable heterogenous catalyst for one step synthesis of 4(3H)-quinazolinones under solvent free conditions publication-title: CATALYSIS COMMUNICATIONS doi: 10.1016/j.catcom.2006.02.026 – volume: 32 start-page: 7243 year: 1991 ident: WOS:A1991GU56900027 article-title: REACTIONS OF AN ENDOPEROXIDE WITH CHIRAL KETONES - DIASTEREOSELECTIVE FORMATION OF 1,2,4-TRIOXANES AND 1,3-DIOXOLANES publication-title: TETRAHEDRON LETTERS – volume: 52 start-page: 3420 year: 2009 ident: WOS:000266296200033 article-title: Antimalarial Peroxide Dyads from Natural Artemisinin and Hydroxyalkylated 1,2,4-Trioxanes publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm9002523 – volume: 57 start-page: 4595 year: 2016 ident: WOS:000384873300021 article-title: Silica-ferric chloride (SiO2-FeCl3) catalyzed selective synthesis of 2-substituted benzimidazole through C-sp2-C-sp3 bond cleavage of beta-ketoesteriamide publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2016.08.099 – volume: 358 start-page: 3586 year: 2016 ident: WOS:000390408200010 article-title: Iron-Catalyzed Annulation of 1,2-Diamines and Diazodicarbonyls for Diverse and Polyfunctionalized Quinoxalines, Pyrazines, and Benzoquinoxalines in Water publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600503 – volume: 46 start-page: 8883 year: 2007 ident: 000413673600025.1 publication-title: Angew. Chem. Int. Ed. – volume: 357 start-page: 2862 year: 2015 ident: WOS:000362527100014 article-title: Iron(III) Chloride-Catalyzed Decarboxylative-Deaminative Functionalization of Phenylglycine: A Tandem Synthesis of Quinazolinones and Benzimidazoles publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201500335 – volume: 433 start-page: 91 year: 2017 ident: WOS:000400562600013 article-title: Mesoporous silica-immobilized FeCl3 as a highly efficient and recyclable catalyst for the nitration of benzene with NO2 to nitrobenzene publication-title: MOLECULAR CATALYSIS doi: 10.1016/j.mcat.2016.12.001 – volume: 70 start-page: 3231 year: 2014 ident: WOS:000335873500003 article-title: Solvent-free Diels-Alder reactions catalyzed by FeCl3 on Aerosil((R)) silica publication-title: TETRAHEDRON doi: 10.1016/j.tet.2014.02.017 – volume: 26 start-page: 735 year: 2015 ident: WOS:000357224900023 article-title: A convenient synthesis of 2-aminocyclohex-1-ene-1-carboxylic esters by FeCl3/SiO2 nanoparticles as robust and efficient catalyst publication-title: CHINESE CHEMICAL LETTERS doi: 10.1016/j.cclet.2015.01.035 – volume: 77 start-page: 1059 year: 2005 ident: WOS:000230007100012 article-title: Photooxygenation in polymer matrices: En route to highly active antimalarial peroxides publication-title: PURE AND APPLIED CHEMISTRY – volume: 358 start-page: 3683 year: 2016 ident: WOS:000390264700002 article-title: Site-Selective Iron(III) Chloride-Catalyzed Arylation of 4-Aryl-4-methoxy-2,5-cyclohexadienones for the Synthesis of Polyarylated Phenols publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600577 – volume: 88 start-page: 39 year: 2017 ident: WOS:000389117500010 article-title: Supported molybdenum on graphene oxide/Fe3O4: An efficient, magnetically separable catalyst for one-pot construction of spiro-oxindole dihydropyridines in deep eutectic solvent under microwave irradiation publication-title: CATALYSIS COMMUNICATIONS doi: 10.1016/j.catcom.2016.09.028 – volume: 5 start-page: 6175 year: 2017 ident: WOS:000405139100063 article-title: Catalyst-Free, Visible-Light Promoted One-Pot Synthesis of Spirooxindole-Pyran Derivatives in Aqueous Ethyl Lactate publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING doi: 10.1021/acssuschemeng.7b01102 – volume: 78 start-page: 26 year: 2016 ident: WOS:000373418700006 article-title: Magnetic carbon nanotube supported Cu (CoFe2O4/CNT-Cu) catalyst: A sustainable catalyst for the synthesis of 3-nitro-2-arylimidazo[1,2-a]pyridines publication-title: CATALYSIS COMMUNICATIONS doi: 10.1016/j.catcom.2016.02.004 – volume: 39 start-page: 580 year: 2009 ident: WOS:000262859200002 article-title: Fluoroboric Acid Adsorbed on Silica-Gel-Catalyzed Synthesis of 14-Aryl-14H-dibenzo[a,j]xanthene Derivatives publication-title: SYNTHETIC COMMUNICATIONS doi: 10.1080/00397910802412842 – volume: 82 start-page: 467 year: 2017 ident: WOS:000398034000019 article-title: Hexagonal Mesoporous Silica-Supported Copper Oxide (CuO/HMS) Catalyst: Synthesis of Primary Amides from Aldehydes in Aqueous Medium publication-title: CHEMPLUSCHEM doi: 10.1002/cplu.201600611 – volume: 77 start-page: 237 year: 1999 ident: WOS:000079823200010 article-title: Photochemical reaction of beta-ionone derivatives in the presence of oxygen. A convenient synthesis of substituted 1,2,4-trioxanes publication-title: CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE – volume: 10 start-page: 629 year: 2015 ident: WOS:000351773300007 article-title: Selective Inhibitors of Glutathione Transferase P1 with Trioxane Structure as Anticancer Agents publication-title: CHEMMEDCHEM doi: 10.1002/cmdc.201402553 – volume: 6 start-page: 3035 year: 2004 ident: WOS:000223581900005 article-title: Application of thiol-olefin co-oxygenation methodology to a new synthesis of the 1,2,4-trioxane pharmacophore publication-title: ORGANIC LETTERS doi: 10.1021/ol0492142 – volume: 10 start-page: 5143 year: 2012 ident: WOS:000305191000020 article-title: Tandem one-pot synthesis of flavans by recyclable silica-HClO4 catalyzed Knoevenagel condensation and [4+2]-Diels-Alder cycloaddition publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c2ob25376c – volume: 69 start-page: 7011 year: 2013 ident: WOS:000322098000010 article-title: One-pot four-component synthesis of highly substituted pyrroles in gluconic acid aqueous solution publication-title: TETRAHEDRON doi: 10.1016/j.tet.2013.06.049 – volume: 20 start-page: 4459 year: 2010 ident: WOS:000279866300036 article-title: 6-(4 '-Aryloxy-phenyl)vinyl-1,2,4-trioxanes: A new series of orally active peroxides effective against multidrug-resistant Plasmodium yoelii in Swiss mice publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2010.06.045 – volume: 58 start-page: 302 year: 2017 ident: WOS:000392896200008 article-title: Synthesis of trans-4,5-diaminocyclopent-2-enones from furfural catalyzed by Er(III) immobilized on silica publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2016.12.002 – volume: 15 start-page: 595 year: 2005 ident: WOS:000226935700020 article-title: Novel spiroanellated 1,2,4-trioxanes with high in vitro antimalarial activities publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2004.11.043 – volume: 2015 start-page: 4349 year: 2015 ident: WOS:000358085100011 article-title: Model Studies on Peroxidic Glutathione Transferase (GST) Inhibitors: C5-Methylated 1,2,4-Trioxanes with C6-Acrylate Side Chains publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.201500326 – volume: 11 start-page: 2613 year: 2013 ident: WOS:000316803900010 article-title: Phosphomolybdic and phosphotungstic acids as efficient catalysts for the synthesis of bridged 1,2,4,5-tetraoxanes from beta-diketones and hydrogen peroxide publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c3ob27239g – volume: 53 start-page: 7587 year: 2010 ident: WOS:000283703000008 article-title: Synthesis and Antimalarial Assessment of a New Series of Orally Active Amino-Functionalized Spiro 1,2,4-Trioxanes publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm100678p – volume: 17 start-page: 3207 year: 2015 ident: WOS:000355925900002 article-title: Silica-nanosphere-based organic-inorganic hybrid nanomaterials: synthesis, functionalization and applications in catalysis publication-title: GREEN CHEMISTRY doi: 10.1039/c5gc00381d – volume: 24 start-page: 173 year: 2013 ident: WOS:000314697700008 article-title: Synthesis of 1,2,4-Trioxepanes and 1,2,4-Trioxanes via H2O2-Mediated Reaction of Tertiary Carbinols publication-title: SYNLETT doi: 10.1055/s-0032-1317958 – start-page: 2430 year: 2011 ident: WOS:000295158200031 article-title: 5-Adamantylated 1,2,4-Trioxanes: Adamantane Position is Crucial for Antiparasitic Activity publication-title: SYNLETT doi: 10.1055/s-0030-1261225 – volume: 17 start-page: 4097 year: 2007 ident: WOS:000248462300001 article-title: Orally active antimalarials: Synthesis and bioevaluation of a new series of steroid-based 1.2.4-trioxanes against multi-drug resistant malaria in mice publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2007.05.055 – volume: 358 start-page: 3471 year: 2016 ident: WOS:000390407300017 article-title: Iron(III)-Catalyzed Peroxide-Mediated C-3 Functionalization of Flavones publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600565 – start-page: 3314 year: 2008 ident: WOS:000260777300018 article-title: Efficient Conversion of Epoxides into beta-Hydroperoxy Alcohols Catalyzed by Antimony Trichloride/SiO2 publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-0028-1083147 – volume: 46 start-page: 685 year: 2016 ident: WOS:000377815800004 article-title: FeCl3-silica: A green approach for the synthesis of nitriles from oximes publication-title: SYNTHETIC COMMUNICATIONS doi: 10.1080/00397911.2016.1167910 – volume: 43 start-page: 1631 year: 2014 ident: WOS:000343272600036 article-title: Eco-efficient, Chemoselective, and Rapid Access to Aminals from Lactams Using Recyclable Silica-supported FeCl3 Catalyst in Green Solvent publication-title: CHEMISTRY LETTERS doi: 10.1246/cl.140624 – volume: 6 start-page: 2854 year: 2014 ident: WOS:000342795000017 article-title: Superparamagnetic CuFeO2 Nanoparticles in Deep Eutectic Solvent: an Efficient and Recyclable Catalytic System for the Synthesis of Imidazo[1,2-a]pyridines publication-title: CHEMCATCHEM doi: 10.1002/cctc.201402415 – volume: 21 start-page: 3540 year: 2009 ident: WOS:000264759200030 article-title: Synthesis of Admantane Substituted Spiro 1,2,4-Trioxanes Using Simple and Cheap Starting Material publication-title: ASIAN JOURNAL OF CHEMISTRY – volume: 6 start-page: 106160 year: 2016 ident: WOS:000389330700014 article-title: Magnetically separable graphene oxide anchored sulfonic acid: a novel, highly efficient and recyclable catalyst for one-pot synthesis of 3,6-di(pyridin-3-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitriles in deep eutectic solvent under microwave irradiation publication-title: RSC ADVANCES doi: 10.1039/c6ra19579b – volume: 19 start-page: 7605 year: 2013 ident: WOS:000319417500038 article-title: Potent Antimalarial 1,2,4-Trioxanes through Perhydrolysis of Epoxides publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201300076 – volume: 355 start-page: 2952 year: 2013 ident: WOS:000328149300029 article-title: Magnetic Nanoparticles (CoFe2O4)-Supported Phosphomolybdate as an Efficient, Green, Recyclable Catalyst for Synthesis of beta-Hydroxy Hydroperoxides publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201300551 – volume: 146 start-page: 165 year: 2015 ident: WOS:000347161300017 article-title: FeCl3-SiO2 promoted one-pot, three-component synthesis of novel 1,5-benzodiazepine derivatives publication-title: MONATSHEFTE FUR CHEMIE doi: 10.1007/s00706-014-1275-9 – volume: 50 start-page: 521 year: 2007 ident: WOS:000243889100013 article-title: New adamantane-based spiro 1,2,4-trioxanes orally effective against rodent and simian malaria publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm0610043 – volume: 354 start-page: 441 year: 2012 ident: WOS:000300448400024 article-title: Triflic Acid-Functionalized Silica-Coated Magnetic Nanoparticles as a Magnetically Separable Catalyst for Synthesis of gem-Dihydroperoxides publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201100561 – volume: 81 start-page: 10088 year: 2016 ident: WOS:000386187500063 article-title: FeCl3-Catalyzed Cross-Dehydrogenative Coupling between Imidazoheterocycles and Oxoaldehydes publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.6b02091 – volume: 288 start-page: 118 year: 2015 ident: WOS:000352252900006 article-title: Silica-decorated magnetic nanocomposites for catalytic applications publication-title: COORDINATION CHEMISTRY REVIEWS doi: 10.1016/j.ccr.2015.01.001 – volume: 36 start-page: 620 year: 2015 ident: WOS:000352678400020 article-title: Nano-sized silica supported FeCl3 as an efficient heterogeneous catalyst for the synthesis of 1,2,4-triazine derivatives publication-title: CHINESE JOURNAL OF CATALYSIS doi: 10.1016/S1872-2067(15)60829-4 – volume: 358 start-page: 3572 year: 2016 ident: WOS:000390408200009 article-title: Iron-Promoted Tandem Cyclization of 1,3-Diynyl Chalcogen Derivatives with Diorganyl Dichalcogenides for the Synthesis of Benzo[b]furan-Fused Selenophenes publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600759 – volume: 56 start-page: 2547 year: 2013 ident: WOS:000317032200031 article-title: Comparative Antimalarial Activities and ADME Profiles of Ozonides (1,2,4-trioxolanes) OZ277, OZ439, and Their 1,2-Dioxolane, 1,2,4-Trioxane, and 1,2,4,5-Tetraoxane Isosteres publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm400004u – volume: 4 start-page: 165 year: 2013 ident: WOS:000315182000009 article-title: Synthesis and Antimalarial Activity of 3,3-Spiroanellated 5,6-Disubstituted 1,2,4-Trioxanes publication-title: ACS MEDICINAL CHEMISTRY LETTERS doi: 10.1021/ml300188t – volume: 4 start-page: 4193 year: 2002 ident: WOS:000179430600003 article-title: Synthesis of antimalarial 1,2,4-trioxanes via photooxygenation of a chiral allylic alcohol publication-title: ORGANIC LETTERS doi: 10.1021/ol026916n – volume: 12 start-page: 1647 year: 2016 ident: WOS:000381258800001 article-title: Rearrangements of organic peroxides and related processes publication-title: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY doi: 10.3762/bjoc.12.162 – volume: 12 start-page: 5745 year: 2004 ident: WOS:000225050500002 article-title: Synthesis and antimalarial activity of 6-cycloalkylvinyl substituted 1,2,4-trioxanes publication-title: BIOORGANIC & MEDICINAL CHEMISTRY doi: 10.1016/j.bmc.2004.08.042 – volume: 21 start-page: 368 year: 2017 ident: WOS:000394169000011 article-title: Silica Supported Ionic Liquid CuCl3-IL-SiO2: A Novel and Highly Efficient Catalyst for Ullmann C-N and C-O Cross-coupling Reactions Under Mild Conditions publication-title: CURRENT ORGANIC CHEMISTRY doi: 10.2174/1385272820666161020150646 – volume: 27 start-page: 1187 year: 2016 ident: WOS:000375004700012 article-title: Site-Selective and Stereoselective C(sp(3))-H Borylation of Alkyl Side Chains of 1,3-Azoles with a Silica-Supported Monophosphine-Iridium Catalyst publication-title: SYNLETT doi: 10.1055/s-0035-1561599 – volume: 80 start-page: 2440 year: 1997 ident: WOS:000071175600012 article-title: The diastereoselective formation of 1,2,4-trioxanes and 1,3-dioxolanes by the reaction of endoperoxides with chiral cyclohexanones publication-title: HELVETICA CHIMICA ACTA – volume: 38 start-page: 2435 year: 2014 ident: WOS:000336821000038 article-title: Nano-CoFe2O4 supported molybdenum as an efficient and magnetically recoverable catalyst for a one-pot, four-component synthesis of functionalized pyrroles publication-title: NEW JOURNAL OF CHEMISTRY doi: 10.1039/c3nj01368e |
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Snippet | An efficient and practical method has been developed for the facile synthesis of 1,2,4‐trioxanes by the condensation of β‐hydroperoxy alcohols and carbonyl... An efficient and practical method has been developed for the facile synthesis of 1,2,4-trioxanes by the condensation of beta-hydroperoxy alcohols and carbonyl... An efficient and practical method has been developed for the facile synthesis of 1,2,4-trioxanes by the condensation of [beta]-hydroperoxy alcohols and... |
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SubjectTerms | 1,2,4-trioxanes Alcohols Carbonyl compounds Carbonyls Catalysis Catalytic activity Chemical synthesis Chemistry Chemistry, Applied Chemistry, Organic Ferric chloride Oxidation Physical Sciences Science & Technology silica-supported iron(III) chloride Silicon dioxide β-hydroperoxy alcohols |
Title | A General and Practical Approach for the Synthesis of 1,2,4‐Trioxanes Catalyzed by Silica‐Ferric Chloride |
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