Palladium-Catalyzed Carbonylative Synthesis of Aryl Formates under Mild Conditions
Aryl formates have been extensively applied as CO sources in CO‐free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium‐catalyzed procedure for the synthesis of aryl formates. Good yields were a...
Saved in:
Published in | ChemCatChem Vol. 8; no. 10; pp. 1788 - 1791 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Blackwell Publishing Ltd
20.05.2016
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Aryl formates have been extensively applied as CO sources in CO‐free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium‐catalyzed procedure for the synthesis of aryl formates. Good yields were achieved under mild reaction conditions with formic acid as the formyl source.
A formyl meeting: A convenient palladium‐catalyzed carbonylation procedure for the synthesis of aryl formates is developed. Good yields are achieved under mild reaction conditions with formic acid as the formyl source. |
---|---|
AbstractList | Abstract
Aryl formates have been extensively applied as CO sources in CO‐free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium‐catalyzed procedure for the synthesis of aryl formates. Good yields were achieved under mild reaction conditions with formic acid as the formyl source. Aryl formates have been extensively applied as CO sources in CO‐free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium‐catalyzed procedure for the synthesis of aryl formates. Good yields were achieved under mild reaction conditions with formic acid as the formyl source. A formyl meeting: A convenient palladium‐catalyzed carbonylation procedure for the synthesis of aryl formates is developed. Good yields are achieved under mild reaction conditions with formic acid as the formyl source. Aryl formates have been extensively applied as CO sources in CO-free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium-catalyzed procedure for the synthesis of aryl formates. Good yields were achieved under mild reaction conditions with formic acid as the formyl source. |
Author | Jiang, Li-Bing Qi, Xinxin Li, Hao-Peng Wu, Xiao-Feng Li, Rui |
Author_xml | – sequence: 1 givenname: Li-Bing surname: Jiang fullname: Jiang, Li-Bing organization: Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, 310018, Hangzhou, P.R. China – sequence: 2 givenname: Rui surname: Li fullname: Li, Rui organization: Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, 310018, Hangzhou, P.R. China – sequence: 3 givenname: Hao-Peng surname: Li fullname: Li, Hao-Peng organization: Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, 310018, Hangzhou, P.R. China – sequence: 4 givenname: Xinxin surname: Qi fullname: Qi, Xinxin organization: Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, 310018, Hangzhou, P.R. China – sequence: 5 givenname: Xiao-Feng surname: Wu fullname: Wu, Xiao-Feng email: xiao-feng.wu@catalysis.de organization: Department of Chemistry, Zhejiang Sci-Tech University, Xiasha Campus, 310018, Hangzhou, P.R. China |
BookMark | eNqFkD1PwzAQhi1UJEphZY7EnGLH-fJYRbQgWihQBJvl2I5wceNiO0D49aQKqtgYTnfD-9zpnmMwqE0tAThDcIwgjC4493wcQZTCrpIDMER5moU4J2Swn3N4BI6dW0OYEpwlQ_CwZFozoZpNWDDPdPstRVAwW5q61cyrDxk8trV_lU65wFTBxLY6mBq7YV66oKmFtMFC6Y4xtVBemdqdgMOKaSdPf_sIPE0vV8VVOL-bXReTecjjCCWhEDyKSDdyhEvJKoR5KTEiGKGI5HEqmOQ8y5OkrCTDDMVE8pylMRQlRpBXeATO-71ba94b6Txdm8bW3UmKsu7rOMpR3KXGfYpb45yVFd1atWG2pQjSnTe680b33jqA9MCn0rL9J02LYlX8ZcOeVc7Lrz3L7BtNs843fb6d0eU9mc1v4IK-4B9iOIN3 |
CitedBy_id | crossref_primary_10_1016_j_tetlet_2018_02_006 crossref_primary_10_1021_acs_oprd_7b00332 crossref_primary_10_1002_chin_201640078 crossref_primary_10_1016_j_mcat_2017_02_003 crossref_primary_10_1039_C7OB01557G crossref_primary_10_1002_cctc_201900011 crossref_primary_10_1002_ejoc_202400009 crossref_primary_10_1039_D2OB02128E crossref_primary_10_1002_ejoc_201900700 crossref_primary_10_1002_aoc_3637 crossref_primary_10_1016_j_jcat_2018_03_028 crossref_primary_10_1039_C9QO00917E crossref_primary_10_1021_acscombsci_9b00090 crossref_primary_10_1002_asia_201600873 crossref_primary_10_1002_asia_201601421 crossref_primary_10_1002_cctc_201700517 crossref_primary_10_1002_ejoc_201801739 crossref_primary_10_1039_C6OB02782B crossref_primary_10_1016_j_jorganchem_2017_03_028 crossref_primary_10_1002_ejoc_201700076 crossref_primary_10_1039_C7QO01081H crossref_primary_10_1039_C6RA13615J crossref_primary_10_1039_C8NJ03173H crossref_primary_10_1007_s00706_018_2331_7 crossref_primary_10_1627_jpi_62_255 crossref_primary_10_1002_slct_201600514 crossref_primary_10_1016_j_tetlet_2016_06_071 crossref_primary_10_1039_C7OB03145A crossref_primary_10_1016_j_gresc_2024_04_008 crossref_primary_10_1002_psc_2998 crossref_primary_10_1016_j_ccr_2017_01_005 crossref_primary_10_3390_nano7120440 crossref_primary_10_1002_cctc_201800532 crossref_primary_10_1002_jlcr_3645 |
Cites_doi | 10.1002/ange.201400793 10.1021/ol5007289 10.1002/ejoc.200700700 10.1002/anie.201303926 10.1016/j.tetlet.2015.09.142 10.1002/anie.200900013 10.1002/anie.201311198 10.1002/anie.201501054 10.1021/ja3114032 10.1002/anie.201400793 10.1021/jo034382d 10.1055/s-0033-1339136 10.1002/ange.201407888 10.1021/ol0354371 10.1002/adsc.201000750 10.1002/anie.200301736 10.1021/ol301192s 10.1002/asia.201500518 10.1002/ange.201311198 10.1055/s-0031-1290350 10.1002/ange.201501054 10.1039/C5CY00691K 10.1021/jo025965a 10.1021/ol026236k 10.1002/anie.201407888 10.1021/ol025836g 10.1002/anie.201404833 10.1021/ol302593z 10.1016/j.tetlet.2008.07.053 10.1002/cctc.201200069 10.1002/ange.200301736 10.1021/jo026591o 10.1021/ol900327x 10.1016/j.jorganchem.2015.12.010 10.1002/chem.201502943 10.1021/ol034862r 10.1002/anie.201100763 10.1021/jo5020118 10.1021/cc049906h 10.1002/chem.201503314 10.1016/j.tetlet.2012.07.057 10.1021/jo102151u 10.1002/ange.201404833 10.1021/ol401092a 10.1002/ange.201303926 10.1039/c2cc33944g 10.1021/ol301850y 10.1021/ja0126881 10.1002/ange.200900013 10.1002/ange.201100763 |
ContentType | Journal Article |
Copyright | 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
Copyright_xml | – notice: 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
DBID | BSCLL AAYXX CITATION |
DOI | 10.1002/cctc.201600165 |
DatabaseName | Istex CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1867-3899 |
EndPage | 1791 |
ExternalDocumentID | 4061532611 10_1002_cctc_201600165 CCTC201600165 ark_67375_WNG_PQ9GLK0M_X |
Genre | shortCommunication |
GrantInformation_xml | – fundername: National Natural Science Foundation of China (NSFC) funderid: 21472174 – fundername: Zhejiang Natural Science Fund for Distinguished Young Scholars funderid: LR16B020002 |
GroupedDBID | 05W 0R~ 1OC 33P 4.4 5DZ 77Q 8-1 A00 AAESR AAHHS AAIHA AANLZ AASGY AAXRX AAZKR ABCUV ABDBF ACAHQ ACCFJ ACCZN ACGFS ACIWK ACPOU ACXBN ACXQS ADBBV ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AENEX AEQDE AEUYR AFBPY AFFPM AFGKR AFZJQ AHBTC AITYG AIURR AIWBW AJBDE ALMA_UNASSIGNED_HOLDINGS ALUQN AMYDB AZVAB BDRZF BFHJK BMXJE BRXPI BSCLL DCZOG DRFUL DRSTM DU5 EBS EJD ESX G-S HGLYW HZ~ I-F LATKE LEEKS LITHE LOXES LUTES LYRES MEWTI MXFUL MXSTM MY~ NNB O9- P2W P4E ROL SUPJJ TUS WBKPD WOHZO WXSBR WYJ XV2 ZZTAW AAYXX CITATION |
ID | FETCH-LOGICAL-c4215-ddc229421c13beaf13cbe31931129846daecc7855bfea3a149ec8a640db310cf3 |
ISSN | 1867-3880 |
IngestDate | Thu Oct 10 20:21:42 EDT 2024 Fri Aug 23 03:42:26 EDT 2024 Sat Aug 24 01:18:03 EDT 2024 Wed Oct 30 09:50:18 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c4215-ddc229421c13beaf13cbe31931129846daecc7855bfea3a149ec8a640db310cf3 |
Notes | ArticleID:CCTC201600165 istex:B42C151777EC0EB8889A3194F563F2EEE85B9791 National Natural Science Foundation of China (NSFC) - No. 21472174 ark:/67375/WNG-PQ9GLK0M-X Zhejiang Natural Science Fund for Distinguished Young Scholars - No. LR16B020002 |
PQID | 1789942814 |
PQPubID | 986343 |
PageCount | 4 |
ParticipantIDs | proquest_journals_1789942814 crossref_primary_10_1002_cctc_201600165 wiley_primary_10_1002_cctc_201600165_CCTC201600165 istex_primary_ark_67375_WNG_PQ9GLK0M_X |
PublicationCentury | 2000 |
PublicationDate | May 20, 2016 |
PublicationDateYYYYMMDD | 2016-05-20 |
PublicationDate_xml | – month: 05 year: 2016 text: May 20, 2016 day: 20 |
PublicationDecade | 2010 |
PublicationPlace | Weinheim |
PublicationPlace_xml | – name: Weinheim |
PublicationTitle | ChemCatChem |
PublicationTitleAlternate | ChemCatChem |
PublicationYear | 2016 |
Publisher | Blackwell Publishing Ltd Wiley Subscription Services, Inc |
Publisher_xml | – name: Blackwell Publishing Ltd – name: Wiley Subscription Services, Inc |
References | K. Natte, A. Dumrath, H. Neumann, M. Beller, Angew. Chem. Int. Ed. 2014, 53, 10090-10094 T. Morimoto, K. Fuji, K. Tsutsumi, K. Kakiuchi, J. Am. Chem. Soc. 2002, 124, 3806-3807 Angew. Chem. 2014, 126, 10254-10258. M. Iizuka, Y. Kondo, Eur. J. Org. Chem. 2007, 5180-5182 T. Ueda, H. Konishi, K. Manabe, Org. Lett. 2012, 14, 4722-4725 Angew. Chem. 2009, 121, 4176-4196 T. Fujihara, T. Hosoki, Y. Katafuchi, T. Iwai, J. Terao, Y. Tsuji, Chem. Commun. 2012, 48, 8012-8014. C. Brancour, T. Fukuyama, Y. Mukai, T. Skrydstrup, I. Ryu, Org. Lett. 2013, 15, 2794-2797. B. Sam, B. Breit, M. J. Krische, Angew. Chem. Int. Ed. 2015, 54, 3267-3274 J. Chen, K. Natte, X.-F. Wu, Tetrahedron Lett. 2015, 56, 6413-6416. J. Hou, J. H. Xie, Q.-L. Zhou, Angew. Chem. Int. Ed. 2015, 54, 6302-6305 X. Qi, L. B. Jiang, H.-P. Li, X. F. Wu, Chem. Eur. J. 2015, 21, 17650-17656 K. Hosoi, K. Nozaki, T. Hiyama, Org. Lett. 2002, 4, 2849-2851. X. Qi, C. L. Li, X.-F. Wu, Chem. Eur. J. 2016, 22, 5835-5838. T. Morimoto, K. Yamasaki, A. Hirano, K. Tsutsumi, N. Kagawa, K. Kakiuchi, Y. Harada, Y. Fukumoto, N. Chatani, T. Nishioka, Org. Lett. 2009, 11, 1777-1780 X. Qi, L. B. Jiang, C. L. Li, R. Li, X. F. Wu, Chem. Asian J. 2015, 10, 1870-1873 T. Ueda, H. Konishi, K. Manabe, Org. Lett. 2012, 14, 5370-5373 Angew. Chem. 2015, 127, 3317-3325. T. Ueda, H. Konishi, K. Manabe, Tetrahedron Lett. 2012, 53, 5171-5175 Angew. Chem. 2013, 125, 8773-8777 S. Cacchi, G. Fabrizi, A. Goggiamani, Org. Lett. 2003, 5, 4269-4272 Q. Liu, H. Zhang, A. Lei, Angew. Chem. Int. Ed. 2011, 50, 10788-10799 L. R. Odell, F. Russo, M. Larhed, Synlett 2012, 685-698; selected examples see Angew. Chem. 2014, 126, 3247-3250 K. T. Neumann, S. R. Laursen, A. T. Lindhardt, B. Bang-Andersen, T. Skrydstrup, Org. Lett. 2014, 16, 2216-2219 A. Brennführer, H. Neumann, M. Beller, Angew. Chem. Int. Ed. 2009, 48, 4114-4133 Angew. Chem. 2004, 116, 5698-5706 Angew. Chem. 2014, 126, 6426-6436 P. Appukkuttan, L. Axelsson, E. V. der Eycken, M. Larhed, Tetrahedron Lett. 2008, 49, 5625-5628 H. Li, H. Neumann, M. Beller, X. F. Wu, Angew. Chem. Int. Ed. 2014, 53, 3183-3186 T. Ueda, H. Konishi, K. Manabe, Angew. Chem. Int. Ed. 2013, 52, 8611-8615 T. Shibata, N. Toshida, K. Takagi, Org. Lett. 2002, 4, 1619-1621 Angew. Chem. 2011, 123, 10978-10989. J. Chen, K. Natte, X.-F. Wu, J. Organomet. Chem. 2016, 803, 9-12 J. Chen, J. B. Feng, K. Natte, X.-F. Wu, Chem. Eur. J. 2015, 21, 16370-16373 Y. Wan, M. Alterman, M. Larhed, A. Hallberg, J. Org. Chem. 2002, 67, 6232-6235 J. Wannberg, M. Larhed, J. Org. Chem. 2003, 68, 5750-5753. Y. Katafuchi, T. Fujihara, T. Iwai, J. Terao, Y. Tsuji, Adv. Synth. Catal. 2011, 353, 475-482 T. Ueda, H. Konishi, K. Manabe, Org. Lett. 2012, 14, 3100-3103 W. Li, X.-F. Wu, J. Org. Chem. 2014, 79, 10410-10416 X.-F. Wu, H. Neumann, ChemCatChem 2012, 4, 447-458 A. Wieckowska, R. Fransson, L. R. Odell, M. Larhed, J. Org. Chem. 2011, 76, 978-981 S. Cacchi, G. Fabrizi, A. Goggiamani, J. Comb. Chem. 2004, 6, 692-694 Angew. Chem. 2015, 127, 6400-6403 H. Konishi, K. Manabe, Synlett 2014, 25, 1971-1986. L. Wu, Q. Liu, R. Jackstell, M. Beller, Angew. Chem. Int. Ed. 2014, 53, 6310-6320 S. Ko, H. Han, S. Chang, Org. Lett. 2003, 5, 2687-2690 S. Korsager, R. H. Taaning, T. Skrydstrup, J. Am. Chem. Soc. 2013, 135, 2891-2894 T. Morimoto, K. Kakiuchi, Angew. Chem. Int. Ed. 2004, 43, 5580-5588 P. Gautam, B. M. Bhanage, Catal. Sci. Technol. 2015, 5, 4663-4702 S. Ko, C. Lee, M.-G. Choi, Y. Na, S. Chang, J. Org. Chem. 2003, 68, 1607-1610 2014 2014; 53 126 2015; 56 2004 2004; 43 116 2015; 5 2012 2016; 803 2009 2009; 48 121 2015; 10 2004; 6 2007 2014; 25 2002; 4 2011; 76 2012; 14 2012; 53 2011; 353 2013 2013; 52 125 2009; 11 2013; 15 2002; 67 2002; 124 2008; 49 2015; 21 2003; 68 2014; 16 2015 2015; 54 127 2003; 5 2014; 79 2013; 135 2016 2011 2011; 50 123 2012; 48 2012; 4 e_1_2_2_2_3 e_1_2_2_24_2 e_1_2_2_47_2 e_1_2_2_4_2 e_1_2_2_22_3 e_1_2_2_49_1 e_1_2_2_4_3 e_1_2_2_22_2 e_1_2_2_6_2 e_1_2_2_20_2 e_1_2_2_2_2 e_1_2_2_41_2 e_1_2_2_6_3 e_1_2_2_8_2 e_1_2_2_28_2 e_1_2_2_43_2 e_1_2_2_26_2 e_1_2_2_45_2 e_1_2_2_13_2 e_1_2_2_36_2 e_1_2_2_11_2 e_1_2_2_38_2 e_1_2_2_51_2 e_1_2_2_19_2 e_1_2_2_30_2 e_1_2_2_32_1 e_1_2_2_17_1 e_1_2_2_15_2 e_1_2_2_34_2 e_1_2_2_3_2 e_1_2_2_5_1 e_1_2_2_48_2 e_1_2_2_23_1 e_1_2_2_21_2 e_1_2_2_1_1 e_1_2_2_40_2 e_1_2_2_42_1 e_1_2_2_29_2 e_1_2_2_7_2 e_1_2_2_27_3 e_1_2_2_7_3 e_1_2_2_27_2 e_1_2_2_44_2 e_1_2_2_9_3 e_1_2_2_9_2 e_1_2_2_25_2 e_1_2_2_46_2 e_1_2_2_14_1 e_1_2_2_35_3 e_1_2_2_12_2 e_1_2_2_37_2 Qi X. (e_1_2_2_31_2) 2016 e_1_2_2_39_2 e_1_2_2_10_1 e_1_2_2_52_1 e_1_2_2_50_2 e_1_2_2_18_2 e_1_2_2_16_2 e_1_2_2_33_2 e_1_2_2_33_3 e_1_2_2_35_2 |
References_xml | – volume: 52 125 start-page: 8611 8773 year: 2013 2013 end-page: 8615 8777 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 5 start-page: 4269 year: 2003 end-page: 4272 publication-title: Org. Lett. – volume: 25 start-page: 1971 year: 2014 end-page: 1986 publication-title: Synlett – volume: 67 start-page: 6232 year: 2002 end-page: 6235 publication-title: J. Org. Chem. – volume: 14 start-page: 4722 year: 2012 end-page: 4725 publication-title: Org. Lett. – volume: 54 127 start-page: 6302 6400 year: 2015 2015 end-page: 6305 6403 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 48 121 start-page: 4114 4176 year: 2009 2009 end-page: 4133 4196 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 53 126 start-page: 10090 10254 year: 2014 2014 end-page: 10094 10258 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 21 start-page: 16370 year: 2015 end-page: 16373 publication-title: Chem. Eur. J. – start-page: 685 year: 2012 end-page: 698 publication-title: Synlett – volume: 68 start-page: 1607 year: 2003 end-page: 1610 publication-title: J. Org. Chem. – start-page: 22 year: 2016 end-page: 5838 publication-title: Chem. Eur. J. – volume: 53 126 start-page: 3183 3247 year: 2014 2014 end-page: 3186 3250 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 10 start-page: 1870 year: 2015 end-page: 1873 publication-title: Chem. Asian J. – volume: 124 start-page: 3806 year: 2002 end-page: 3807 publication-title: J. Am. Chem. Soc. – volume: 49 start-page: 5625 year: 2008 end-page: 5628 publication-title: Tetrahedron Lett. – volume: 6 start-page: 692 year: 2004 end-page: 694 publication-title: J. Comb. Chem. – volume: 21 start-page: 17650 year: 2015 end-page: 17656 publication-title: Chem. Eur. J. – volume: 15 start-page: 2794 year: 2013 end-page: 2797 publication-title: Org. Lett. – volume: 5 start-page: 4663 year: 2015 end-page: 4702 publication-title: Catal. Sci. Technol. – volume: 16 start-page: 2216 year: 2014 end-page: 2219 publication-title: Org. Lett. – volume: 54 127 start-page: 3267 3317 year: 2015 2015 end-page: 3274 3325 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 76 start-page: 978 year: 2011 end-page: 981 publication-title: J. Org. Chem. – volume: 56 start-page: 6413 year: 2015 end-page: 6416 publication-title: Tetrahedron Lett. – start-page: 5180 year: 2007 end-page: 5182 publication-title: Eur. J. Org. Chem. – volume: 135 start-page: 2891 year: 2013 end-page: 2894 publication-title: J. Am. Chem. Soc. – volume: 48 start-page: 8012 year: 2012 end-page: 8014 publication-title: Chem. Commun. – volume: 53 start-page: 5171 year: 2012 end-page: 5175 publication-title: Tetrahedron Lett. – volume: 353 start-page: 475 year: 2011 end-page: 482 publication-title: Adv. Synth. Catal. – volume: 803 start-page: 9 year: 2016 end-page: 12 publication-title: J. Organomet. Chem. – volume: 14 start-page: 3100 year: 2012 end-page: 3103 publication-title: Org. Lett. – volume: 68 start-page: 5750 year: 2003 end-page: 5753 publication-title: J. Org. Chem. – volume: 4 start-page: 447 year: 2012 end-page: 458 publication-title: ChemCatChem – volume: 43 116 start-page: 5580 5698 year: 2004 2004 end-page: 5588 5706 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 4 start-page: 2849 year: 2002 end-page: 2851 publication-title: Org. Lett. – volume: 14 start-page: 5370 year: 2012 end-page: 5373 publication-title: Org. Lett. – volume: 11 start-page: 1777 year: 2009 end-page: 1780 publication-title: Org. Lett. – volume: 79 start-page: 10410 year: 2014 end-page: 10416 publication-title: J. Org. Chem. – volume: 5 start-page: 2687 year: 2003 end-page: 2690 publication-title: Org. Lett. – volume: 50 123 start-page: 10788 10978 year: 2011 2011 end-page: 10799 10989 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 53 126 start-page: 6310 6426 year: 2014 2014 end-page: 6320 6436 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 4 start-page: 1619 year: 2002 end-page: 1621 publication-title: Org. Lett. – ident: e_1_2_2_7_3 doi: 10.1002/ange.201400793 – ident: e_1_2_2_50_2 doi: 10.1021/ol5007289 – ident: e_1_2_2_32_1 – ident: e_1_2_2_30_2 – ident: e_1_2_2_43_2 doi: 10.1002/ejoc.200700700 – ident: e_1_2_2_35_2 doi: 10.1002/anie.201303926 – ident: e_1_2_2_48_2 doi: 10.1016/j.tetlet.2015.09.142 – ident: e_1_2_2_23_1 – ident: e_1_2_2_2_2 doi: 10.1002/anie.200900013 – ident: e_1_2_2_33_2 doi: 10.1002/anie.201311198 – ident: e_1_2_2_27_2 doi: 10.1002/anie.201501054 – ident: e_1_2_2_26_2 doi: 10.1021/ja3114032 – ident: e_1_2_2_7_2 doi: 10.1002/anie.201400793 – ident: e_1_2_2_13_2 doi: 10.1021/jo034382d – ident: e_1_2_2_17_1 – start-page: 22 year: 2016 ident: e_1_2_2_31_2 publication-title: Chem. Eur. J. contributor: fullname: Qi X. – ident: e_1_2_2_52_1 doi: 10.1055/s-0033-1339136 – ident: e_1_2_2_14_1 – ident: e_1_2_2_9_3 doi: 10.1002/ange.201407888 – ident: e_1_2_2_24_2 doi: 10.1021/ol0354371 – ident: e_1_2_2_40_2 doi: 10.1002/adsc.201000750 – ident: e_1_2_2_6_2 doi: 10.1002/anie.200301736 – ident: e_1_2_2_38_2 doi: 10.1021/ol301192s – ident: e_1_2_2_28_2 doi: 10.1002/asia.201500518 – ident: e_1_2_2_33_3 doi: 10.1002/ange.201311198 – ident: e_1_2_2_11_2 doi: 10.1055/s-0031-1290350 – ident: e_1_2_2_27_3 doi: 10.1002/ange.201501054 – ident: e_1_2_2_8_2 doi: 10.1039/C5CY00691K – ident: e_1_2_2_12_2 doi: 10.1021/jo025965a – ident: e_1_2_2_16_2 doi: 10.1021/ol026236k – ident: e_1_2_2_9_2 doi: 10.1002/anie.201407888 – ident: e_1_2_2_49_1 – ident: e_1_2_2_19_2 doi: 10.1021/ol025836g – ident: e_1_2_2_22_2 doi: 10.1002/anie.201404833 – ident: e_1_2_2_36_2 doi: 10.1021/ol302593z – ident: e_1_2_2_44_2 doi: 10.1016/j.tetlet.2008.07.053 – ident: e_1_2_2_1_1 – ident: e_1_2_2_3_2 doi: 10.1002/cctc.201200069 – ident: e_1_2_2_6_3 doi: 10.1002/ange.200301736 – ident: e_1_2_2_39_2 doi: 10.1021/jo026591o – ident: e_1_2_2_20_2 doi: 10.1021/ol900327x – ident: e_1_2_2_46_2 doi: 10.1016/j.jorganchem.2015.12.010 – ident: e_1_2_2_29_2 doi: 10.1002/chem.201502943 – ident: e_1_2_2_15_2 doi: 10.1021/ol034862r – ident: e_1_2_2_42_1 – ident: e_1_2_2_4_2 doi: 10.1002/anie.201100763 – ident: e_1_2_2_21_2 doi: 10.1021/jo5020118 – ident: e_1_2_2_25_2 doi: 10.1021/cc049906h – ident: e_1_2_2_47_2 doi: 10.1002/chem.201503314 – ident: e_1_2_2_37_2 doi: 10.1016/j.tetlet.2012.07.057 – ident: e_1_2_2_45_2 doi: 10.1021/jo102151u – ident: e_1_2_2_22_3 doi: 10.1002/ange.201404833 – ident: e_1_2_2_51_2 doi: 10.1021/ol401092a – ident: e_1_2_2_35_3 doi: 10.1002/ange.201303926 – ident: e_1_2_2_5_1 – ident: e_1_2_2_41_2 doi: 10.1039/c2cc33944g – ident: e_1_2_2_34_2 doi: 10.1021/ol301850y – ident: e_1_2_2_18_2 doi: 10.1021/ja0126881 – ident: e_1_2_2_2_3 doi: 10.1002/ange.200900013 – ident: e_1_2_2_10_1 – ident: e_1_2_2_4_3 doi: 10.1002/ange.201100763 |
SSID | ssj0069375 |
Score | 2.3446057 |
Snippet | Aryl formates have been extensively applied as CO sources in CO‐free carbonylation reactions. However, there are no catalytic synthetic procedures for their... Abstract Aryl formates have been extensively applied as CO sources in CO‐free carbonylation reactions. However, there are no catalytic synthetic procedures for... Aryl formates have been extensively applied as CO sources in CO-free carbonylation reactions. However, there are no catalytic synthetic procedures for their... |
SourceID | proquest crossref wiley istex |
SourceType | Aggregation Database Publisher |
StartPage | 1788 |
SubjectTerms | carbonylation CO free coupling reactions formates palladium |
Title | Palladium-Catalyzed Carbonylative Synthesis of Aryl Formates under Mild Conditions |
URI | https://api.istex.fr/ark:/67375/WNG-PQ9GLK0M-X/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcctc.201600165 https://www.proquest.com/docview/1789942814 |
Volume | 8 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF6F5AAXVF4itCAfEByqhfi9PiaGNIKmSksqcrPWuxvVonWQm0hNfwK_mhmvnygVhYvjrCw7nvl2dmYy-w0hbwMw-ooHjDpS-tQRitM48F0qmOCOK0DjHDc4T0-8ybnzZeEuOp1fjaqlzTr-IG537iv5H63CGOgVd8n-g2arm8IAnIN-4QgahuO9dDzDLLhMNlc0xCzM9hbTtTyLsdpcE3p_26bg4RWkI8Nse3k4zp1UdZ03wM0Op8mlxG1_MqkzdyVxwYW6gvviR1VnkxTp5eOEjspFD8t58pqAs03SHpjwFZ2p-rLTfHSRpDcF33eRbjA9_KfcGtyVVtRpsroACU0oA9OLFDN6hWmO6VZIpd1lTXgNGkbU9HWnv2JBRgLVncZek8cKkVNRmui56bYTbVbtP1a7qgaRZz-wqM13o-8nR9HsNDg6_jqYRosHpGeB0WJd0huOPo3G5brugSOHBbHV-5UUoAPrY_s3tFycHs7Wm1b80oyCcjdmvkceF_GHMdRgekI6Kn1KHoZl279n5GwHqIwWqIwKVMZqaSCojBJURg4qA0Fl1KB6Ts7Hn-fhhBaNN6hwwAWkUgrLCuBUmHas-NK0RazAVtvonIPDKjlMfJ-5brxU3OYQZCvBuOcMZAzRgljaL0g3XaXqJTFcl_mBx3wuHQi8XYtxZfmWF0gRYJf7uE_el7KKfmp-lUgzaVsRSjWqpNon73JRVpfdpcA-OShlHRWT9ToCTAXwRsx0-sTK5f-Xx0VhOA-rb6_u-_B98qieNQeku8426jW4rev4TYGn32_OlfI |
link.rule.ids | 315,783,787,27938,27939 |
linkProvider | EBSCOhost |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Palladium-Catalyzed+Carbonylative+Synthesis+of+Aryl+Formates+under+Mild+Conditions&rft.jtitle=ChemCatChem&rft.au=Jiang%2C+Li-Bing&rft.au=Li%2C+Rui&rft.au=Li%2C+Hao-Peng&rft.au=Qi%2C+Xinxin&rft.date=2016-05-20&rft.pub=Blackwell+Publishing+Ltd&rft.issn=1867-3880&rft.eissn=1867-3899&rft.volume=8&rft.issue=10&rft.spage=1788&rft.epage=1791&rft_id=info:doi/10.1002%2Fcctc.201600165&rft.externalDBID=n%2Fa&rft.externalDocID=ark_67375_WNG_PQ9GLK0M_X |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1867-3880&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1867-3880&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1867-3880&client=summon |