[4+2] Cycloaddition of Ketenes with N-Benzoyldiazenes Catalyzed by N-Heterocyclic Carbenes
Enantioselectivity switch: A catalytic enantioselective [4+2] cycloaddition reaction of alkylarylketenes with N‐aryl‐N′‐benzoyldiazenes or N,N′‐dibenzoyldiazenes to give 1,3,4‐oxadiazin‐6‐ones 1 was developed by employing N‐heterocyclic carbene (NHC) catalysts. The enantioselectivities could be swit...
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| Published in | Angewandte Chemie (International ed.) Vol. 48; no. 1; pp. 192 - 195 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
Wiley-VCH Verlag
01.01.2009
WILEY-VCH Verlag WILEY‐VCH Verlag Wiley |
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| Abstract | Enantioselectivity switch: A catalytic enantioselective [4+2] cycloaddition reaction of alkylarylketenes with N‐aryl‐N′‐benzoyldiazenes or N,N′‐dibenzoyldiazenes to give 1,3,4‐oxadiazin‐6‐ones 1 was developed by employing N‐heterocyclic carbene (NHC) catalysts. The enantioselectivities could be switched for most reactions by changing the substituents on the NHC catalyst. TBS=tert‐butyldimethylsilyl, Mes=2,4,6‐trimethylphenyl. |
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| AbstractList | Enantioselectivity switch: A catalytic enantioselective [4+2] cycloaddition reaction of alkylarylketenes with N‐aryl‐N′‐benzoyldiazenes or N,N′‐dibenzoyldiazenes to give 1,3,4‐oxadiazin‐6‐ones 1 was developed by employing N‐heterocyclic carbene (NHC) catalysts. The enantioselectivities could be switched for most reactions by changing the substituents on the NHC catalyst. TBS=tert‐butyldimethylsilyl, Mes=2,4,6‐trimethylphenyl. |
| Author | Ye, Song Shao, Pan-Lin He, Lin Huang, Xue-Liang |
| Author_xml | – sequence: 1 fullname: Huang, Xue-Liang – sequence: 2 fullname: He, Lin – sequence: 3 fullname: Shao, Pan-Lin – sequence: 4 fullname: Ye, Song |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19040237$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1002/anie.200802439 10.1002/anie.200500098 10.1021/jo071247i 10.1002/chem.200801165 10.1002/ejoc.200500452 10.1039/b611091f 10.1016/j.tetasy.2008.05.017 10.1021/ar030050j 10.1021/jo801494f 10.1002/anie.200603380 10.1055/s-2008-1067216 10.1021/ol702759b 10.1016/S0040-4020(03)00491-5 10.1002/anie.200500761 10.1021/cr068372z 10.1039/b800857b 10.1016/S0040-4039(01)98119-5 10.1021/jo00923a011 10.1002/ange.200500761 10.1055/sos-SD-023-00002 10.1021/ja00415a046 10.1016/S0040-4039(01)97825-6 10.1016/S0040-4039(01)97497-0 10.1002/ange.200500098 10.1016/B978-008044992-0.00808-7 10.1016/S0040-4039(01)86704-6 10.1002/ange.200502617 10.1002/ange.200603380 10.1039/B611091F 10.1021/ja00415a047 10.1002/anie.200502617 10.1016/S0040-4039(01)98593-4 10.1016/S0040-4039(00)70256-5 10.1002/ange.200802439 10.1016/S0040-4039(01)98120-1 10.1021/jo00186a026 10.1002/jhet.5570200426 |
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| Copyright | Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim |
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| Keywords | enantioselectivity HIGHLY ENANTIOSELECTIVE SYNTHESIS cycloaddition ASYMMETRIC-SYNTHESIS AZA-BETA-LACTAMS ketenes carbenes BAYLIS-HILLMAN REACTION ORGANOCATALYSIS ENONES synthetic methods |
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| Notes | http://dx.doi.org/10.1002/anie.200804487 Chinese Academy of Sciences istex:6195A0271C2732184168CD661489A8F8D96E37D5 ArticleID:ANIE200804487 We are grateful to the Chinese Academy of Sciences and the Natural Sciences Foundation of China (No 20602036) for the financial support. Natural Sciences Foundation of China - No. 20602036 ark:/67375/WNG-KVCF69K0-T ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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| References | R. K. Orr, M. A. Calter, Tetrahedron 2003, 59, 3545. H. Vogt, S. Bräse, Org. Biomol. Chem. 2007, 5, 406. Angew. Chem. Int. Ed. 2005, 44, 2632 J. Firl, S. Sommer, Tetrahedron Lett. 1970, 11, 1929 N. Marion, S. Diez-Gonzalez, S. P. Nolan, Angew. Chem. 2007, 119, 3046 F. Bassman, R. G. Jones, J. Chem. Soc. Perkin Trans. 2 1983, 1759 W.-D. Pfeiffer, Comprehensive Heterocyclic Chemistry III, Vol. 9 (Eds.: A. Katritzky, C. Ramsden, E. Scriven, R. Taylor), Elsevier Science, Dordrecht, 2008, pp. 401-455. J. J. Tufariello, T. F. Mich, P. S. Miller, Tetrahedron Lett. 1966, 7, 2293. J. Firl, S. Sommer, Tetrahedron Lett. 1970, 11, 1925 Angew. Chem. Int. Ed. 2005, 44, 7506 E. C. Taylor, H. M. L. Davies, W. T. Lavell, J. Org. Chem. 1984, 49, 2204. L. He, Y.-R. Zhang, X.-L. Huang, S. Ye, Synthesis 2008, 2825 E. C. Taylor, H. M. L. Davies, R. J. Clements, H. Yanagisawa, N. F. Haley, J. Am. Chem. Soc. 1981, 103, 7660 T. T. Tidwell, Ketenes, 2nd ed., Wiley, Hoboken, NJ, 2006 T. T. Tidwell, Eur. J. Org. Chem. 2006, 563 A. I. El-Shenawy, A. A. Aly, Egypt. J. Chem. 2005, 48, 781 J. M. Berlin, G. C. Fu, Angew. Chem. 2008, 120, 7156 T. T. Tidwell, Angew. Chem. 2005, 117, 5926 J. P. Freeman, D. L. Surbey, J. E. Kassner, Tetrahedron Lett. 1970, 11, 3797 C. Cativiela, M. D. Diaze-de-villegas, Tetrahedron: Asymmetry 2007, 5, 406 L. He, T.-Y. Jian, S. Ye, J. Org. Chem. 2007, 72, 7466. Y. R. Zhang, L. He, X. Wu, P. L. Shao, S. Ye, Org. Lett. 2008, 10, 277 D. Enders, T. Balensiefer, Acc. Chem. Res. 2004, 37, 534. B. C. Kerber, T. J. Ryan, S. D. Hsu, J. Org. Chem. 1974, 39, 1215. C. Farina, G. Pifferi, F. Nasi, M. Pinza, J. Heterocycl. Chem. 1983, 20, 979 Angew. Chem. Int. Ed. 2008, 47, 7048. N. Duguet, C. D. Campbell, A. M. Z. Slawin, A. D. Smith, Org. Biomol. Chem. 2008, 6, 1108. E. C. Taylor, R. J. Clemens, H. M. L. Davies, N. F. Haley, J. Am. Chem. Soc. 1981, 103, 7659 L. He, H. Lv, Y.-R. Zhang, S. Ye, J. Org. Chem. 2008, 73, 8101. Angew. Chem. Int. Ed. 2005, 44, 5778 J. Markert, E. Fahr, Tetrahedron Lett. 1970, 11, 769 K. Zeitler, Angew. Chem. 2005, 117, 7674 Y.-R. Zhang, H. Lv, D. Zhou, S. Ye, Chem. Eur. J. 2008, 14, 8473. A. Bigotto, M. Forchiassin, A. Risaliti, C. Russo, Tetrahedron Lett. 1979, 20, 4761 F. Firl, S. Sommer, Tetrahedron Lett. 1971, 12, 4193 M. Christmann, Angew. Chem. 2005, 117, 2688 Angew. Chem. Int. Ed. 2007, 46, 2988 In addition to our report (reference [3a]), Enders et al. have also reported the synthesis of NHC precursor 4 a from L-pyroglutamic acid: D. Enders, J. Han, Tetrahedron: Asymmetry 2008, 19, 1367. D. Enders, O. Niemeier, A. Henseler, Chem. Rev. 2007, 107, 5606 2007; 107 1984; 49 1981; 103 1966; 7 2008; 19 2008; 14 1970; 11 2008 2003; 59 2006 2008; 10 2008; 6 2007; 72 2005; 48 2008; 73 1974; 39 2004; 37 1971; 12 1983; 20 1983 2007; 5 2007 2007; 119 46 1979; 20 2008 2008; 120 47 2005 2005; 117 44 Orr, RK (WOS:000182784200001) 2003; 59 BIGOTTO A (WOS:000262420700027.4) 1979; 20 Vogt, H (WOS:000243746100003) 2007; 5 TAYLOR, EC (WOS:A1981MT86500047) 1981; 103 ZEITLER K (WOS:000262420700027.37) 2005; 117 KERBER BC (WOS:000262420700027.21) 1974; 39 Tidwell, TT (WOS:000297764600008) 2006 FIRL J (WOS:000262420700027.16) 1970; 11 FIRL F (WOS:000262420700027.15) 1971; 12 Tidwell, TT (WOS:000231989600004) 2005; 44 Marion, N (WOS:000246139400010) 2007; 46 BASSMAN F (WOS:000262420700027.1) 1983 Zhang, YR (WOS:000252294500032) 2008; 10 TUFARIELLO JJ (WOS:000262420700027.34) 1966; 7 BERLIN JM (WOS:000262420700027.2) 2008; 120 He, L (WOS:000249371200061) 2007; 72 Tidwell, TT (WOS:000235349000001) 2006; 2006 Berlin, JM (WOS:000259041000019) 2008; 47 He, L (WOS:000259301000020) 2008 Zhang, YR (WOS:000260035900006) 2008; 14 He, L (WOS:000259973900039) 2008; 73 Enders, D (WOS:000257811900013) 2008; 19 Enders, D (WOS:000251583300006) 2007; 107 ZEITLER K (WOS:000262420700027.36) 2005; 44 Enders, D (WOS:000223385800007) 2004; 37 Duguet, N (WOS:000253909000025) 2008; 6 CATIVIELA C (WOS:000262420700027.5) 2007; 5 Christmann, M (WOS:000228957600002) 2005; 44 TIDWELL TT (WOS:000262420700027.32) 2005; 117 MARKERT J (WOS:000262420700027.24) 1970; 11 MARION N (WOS:000262420700027.23) 2007; 119 FARINA, C (WOS:A1983RE04100026) 1983; 20 FREEMAN JP (WOS:000262420700027.17) 1970; 11 TAYLOR, EC (WOS:A1984SW65900026) 1984; 49 TAYLOR, EC (WOS:A1981MT86500046) 1981; 103 ELSHENAWY AI (WOS:000262420700027.9) 2005; 48 FIRL J (WOS:000262420700027.14) 1970; 11 CHRISTMANN M (WOS:000262420700027.6) 2005; 117 PFEIFFER WD (WOS:000262420700027.26) 2008; 9 El‐Shenawy A. I. (e_1_2_3_21_2) 2005; 48 e_1_2_3_4_2 e_1_2_3_16_2 e_1_2_3_37_2 e_1_2_3_2_2 e_1_2_3_18_2 e_1_2_3_39_2 e_1_2_3_8_3 e_1_2_3_10_3 e_1_2_3_8_2 e_1_2_3_12_2 e_1_2_3_33_2 e_1_2_3_6_2 e_1_2_3_14_2 e_1_2_3_35_2 e_1_2_3_10_2 e_1_2_3_31_2 Bassman F. (e_1_2_3_36_2) 1983 e_1_2_3_26_2 e_1_2_3_28_2 e_1_2_3_22_2 e_1_2_3_45_2 e_1_2_3_24_2 e_1_2_3_47_2 e_1_2_3_41_2 e_1_2_3_20_2 e_1_2_3_43_2 He L. (e_1_2_3_44_2) 2008 e_1_2_3_19_2 e_1_2_3_1_2 e_1_2_3_5_2 e_1_2_3_15_2 e_1_2_3_38_2 e_1_2_3_3_3 e_1_2_3_3_2 e_1_2_3_17_2 e_1_2_3_9_2 e_1_2_3_11_2 e_1_2_3_34_2 e_1_2_3_32_3 e_1_2_3_7_2 e_1_2_3_13_2 e_1_2_3_32_2 e_1_2_3_9_3 Cativiela C. (e_1_2_3_30_2) 2007; 5 e_1_2_3_27_2 e_1_2_3_29_2 e_1_2_3_23_2 e_1_2_3_25_2 e_1_2_3_46_2 e_1_2_3_40_2 e_1_2_3_42_2 |
| References_xml | – volume: 14 start-page: 8473 year: 2008 publication-title: Chem. Eur. J. – volume: 103 start-page: 7659 year: 1981 publication-title: J. Am. Chem. Soc. – volume: 107 start-page: 5606 year: 2007 publication-title: Chem. Rev. – volume: 11 start-page: 1925 year: 1970 publication-title: Tetrahedron Lett. – volume: 73 start-page: 8101 year: 2008 publication-title: J. Org. Chem. – volume: 11 start-page: 1929 year: 1970 publication-title: Tetrahedron Lett. – volume: 117 44 start-page: 7674 7506 year: 2005 2005 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 59 start-page: 3545 year: 2003 publication-title: Tetrahedron – volume: 37 start-page: 534 year: 2004 publication-title: Acc. Chem. Res. – volume: 48 start-page: 781 year: 2005 publication-title: Egypt. J. Chem. – volume: 20 start-page: 4761 year: 1979 publication-title: Tetrahedron Lett. – volume: 5 start-page: 406 year: 2007 publication-title: Org. Biomol. Chem. – volume: 117 44 start-page: 2688 2632 year: 2005 2005 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 49 start-page: 2204 year: 1984 publication-title: J. Org. Chem. – volume: 11 start-page: 3797 year: 1970 publication-title: Tetrahedron Lett. – volume: 6 start-page: 1108 year: 2008 publication-title: Org. Biomol. Chem. – volume: 12 start-page: 4193 year: 1971 publication-title: Tetrahedron Lett. – volume: 11 start-page: 769 year: 1970 publication-title: Tetrahedron Lett. – start-page: 401 year: 2008 end-page: 455 – start-page: 563 year: 2006 publication-title: Eur. J. Org. Chem. – volume: 120 47 start-page: 7156 7048 year: 2008 2008 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 72 start-page: 7466 year: 2007 publication-title: J. Org. Chem. – volume: 103 start-page: 7660 year: 1981 publication-title: J. Am. Chem. Soc. – volume: 5 start-page: 406 year: 2007 publication-title: Tetrahedron: Asymmetry – volume: 7 start-page: 2293 year: 1966 publication-title: Tetrahedron Lett. – start-page: 1759 year: 1983 publication-title: J. Chem. Soc. Perkin Trans. 2 – year: 2006 – volume: 19 start-page: 1367 year: 2008 publication-title: Tetrahedron: Asymmetry – volume: 10 start-page: 277 year: 2008 publication-title: Org. Lett. – volume: 39 start-page: 1215 year: 1974 publication-title: J. Org. Chem. – volume: 20 start-page: 979 year: 1983 publication-title: J. Heterocycl. Chem. – volume: 117 44 start-page: 5926 5778 year: 2005 2005 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – start-page: 2825 year: 2008 publication-title: Synthesis – volume: 119 46 start-page: 3046 2988 year: 2007 2007 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 103 start-page: 7660 year: 1981 ident: WOS:A1981MT86500047 article-title: 3-OXO-1,2-DIAZETIDINIUM TOSYLATE publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: TAYLOR, EC – volume: 5 start-page: 406 year: 2007 ident: WOS:000262420700027.5 publication-title: TETRAHEDRON-ASYMMETR contributor: fullname: CATIVIELA C – volume: 47 start-page: 7048 year: 2008 ident: WOS:000259041000019 article-title: Enantioselective nucleophilic catalysis: The synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200802439 contributor: fullname: Berlin, JM – volume: 44 start-page: 5778 year: 2005 ident: WOS:000231989600004 article-title: The first century of ketenes (1905-2005): The birth of a versatile family of reactive intermediates publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200500098 contributor: fullname: Tidwell, TT – volume: 11 start-page: 3797 year: 1970 ident: WOS:000262420700027.17 publication-title: TETRAHEDRON LETT contributor: fullname: FREEMAN JP – volume: 72 start-page: 7466 year: 2007 ident: WOS:000249371200061 article-title: N-heterocyclic carbene catalyzed Aza-Morita-Baylis-Hillman reaction of cyclic enones with N-tosylarylimines publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo071247i contributor: fullname: He, L – volume: 11 start-page: 769 year: 1970 ident: WOS:000262420700027.24 publication-title: TETRAHEDRON LETT contributor: fullname: MARKERT J – volume: 14 start-page: 8473 year: 2008 ident: WOS:000260035900006 article-title: Chiral N-Heterocyclic Carbene-Catalyzed Formal [4+2] Cycloaddition of Ketenes with Enones: Highly Enantioselective Synthesis of trans- and cis-delta-Lactones publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200801165 contributor: fullname: Zhang, YR – volume: 11 start-page: 1929 year: 1970 ident: WOS:000262420700027.16 publication-title: TETRAHEDRON LETT contributor: fullname: FIRL J – volume: 2006 start-page: 563 year: 2006 ident: WOS:000235349000001 article-title: Ketene chemistry after 100 years: Ready for a new century publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.200500452 contributor: fullname: Tidwell, TT – volume: 7 start-page: 2293 year: 1966 ident: WOS:000262420700027.34 publication-title: TETRAHEDRON LETT contributor: fullname: TUFARIELLO JJ – start-page: 1 year: 2006 ident: WOS:000297764600008 article-title: Ketenes II publication-title: KETENES II contributor: fullname: Tidwell, TT – volume: 117 start-page: 5926 year: 2005 ident: WOS:000262420700027.32 publication-title: ANGEW CHEM contributor: fullname: TIDWELL TT – volume: 119 start-page: 3046 year: 2007 ident: WOS:000262420700027.23 publication-title: ANGEW CHEM contributor: fullname: MARION N – volume: 9 start-page: 401 year: 2008 ident: WOS:000262420700027.26 publication-title: COMPREHENSIVE HETERO contributor: fullname: PFEIFFER WD – volume: 120 start-page: 7156 year: 2008 ident: WOS:000262420700027.2 publication-title: ANGEW CHEM contributor: fullname: BERLIN JM – volume: 11 start-page: 1925 year: 1970 ident: WOS:000262420700027.14 publication-title: TETRAHEDRON LETT contributor: fullname: FIRL J – volume: 5 start-page: 406 year: 2007 ident: WOS:000243746100003 article-title: Recent approaches towards the asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/b611091f contributor: fullname: Vogt, H – volume: 49 start-page: 2204 year: 1984 ident: WOS:A1984SW65900026 article-title: N-ACYLATION VS O-ACYLATION OF 1,2-DIAZETIDIN-3-ONE - 4,5-DIHYDRO-1,3-OXADIAZIN-6-ONES BY RING ENLARGEMENT publication-title: JOURNAL OF ORGANIC CHEMISTRY contributor: fullname: TAYLOR, EC – volume: 19 start-page: 1367 year: 2008 ident: WOS:000257811900013 article-title: Synthesis of enantiopure triazolium salts from pyroglutamic acid and their evaluation in the benzoin condensation publication-title: TETRAHEDRON-ASYMMETRY doi: 10.1016/j.tetasy.2008.05.017 contributor: fullname: Enders, D – volume: 37 start-page: 534 year: 2004 ident: WOS:000223385800007 article-title: Nucleophilic carbenes in asymmetric organocatalysis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar030050j contributor: fullname: Enders, D – volume: 73 start-page: 8101 year: 2008 ident: WOS:000259973900039 article-title: Formal cycloaddition of disubstituted ketenes with 2-oxoaldehydes catalyzed by chiral N-heterocyclic carbenes publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo801494f contributor: fullname: He, L – volume: 12 start-page: 4193 year: 1971 ident: WOS:000262420700027.15 publication-title: TETRAHEDRON LETT contributor: fullname: FIRL F – volume: 39 start-page: 1215 year: 1974 ident: WOS:000262420700027.21 publication-title: J ORG CHEM contributor: fullname: KERBER BC – volume: 103 start-page: 7659 year: 1981 ident: WOS:A1981MT86500046 article-title: FORMATION OF MONOCYCLIC AND BICYCLIC AZA-BETA-LACTAMS AND OTHER NOVEL HETEROCYCLES FROM 1-(DIPHENYLMETHYLENE)-3-OXO-1,2-DIAZETIDINIUM INNER SALT publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: TAYLOR, EC – start-page: 1759 year: 1983 ident: WOS:000262420700027.1 publication-title: J CHEM SOC P2 contributor: fullname: BASSMAN F – volume: 20 start-page: 4761 year: 1979 ident: WOS:000262420700027.4 publication-title: TETRAHEDRON LETT contributor: fullname: BIGOTTO A – volume: 48 start-page: 781 year: 2005 ident: WOS:000262420700027.9 publication-title: EGYPT J CHEM contributor: fullname: ELSHENAWY AI – volume: 46 start-page: 2988 year: 2007 ident: WOS:000246139400010 article-title: N-heterocyclic carbenes as organocatalysts publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200603380 contributor: fullname: Marion, N – volume: 117 start-page: 268 year: 2005 ident: WOS:000262420700027.6 publication-title: ANGEW CHEM contributor: fullname: CHRISTMANN M – start-page: 2825 year: 2008 ident: WOS:000259301000020 article-title: Chiral bifunctional N-heterocyclic carbenes: Synthesis and application in the aza-Morita-Baylis-Hillman reaction publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-2008-1067216 contributor: fullname: He, L – volume: 44 start-page: 7056 year: 2005 ident: WOS:000262420700027.36 publication-title: ANGEW CHEM INT EDIT contributor: fullname: ZEITLER K – volume: 10 start-page: 277 year: 2008 ident: WOS:000252294500032 article-title: Chiral N-heterocyclic carbene catalyzed Staudinger reaction of ketenes with imines: Highly enantioselective synthesis of N-boc beta-lactams publication-title: ORGANIC LETTERS doi: 10.1021/ol702759b contributor: fullname: Zhang, YR – volume: 117 start-page: 7674 year: 2005 ident: WOS:000262420700027.37 publication-title: ANGEW CHEM contributor: fullname: ZEITLER K – volume: 59 start-page: 3545 year: 2003 ident: WOS:000182784200001 article-title: Asymmetric synthesis using ketenes publication-title: TETRAHEDRON doi: 10.1016/S0040-4020(03)00491-5 contributor: fullname: Orr, RK – volume: 44 start-page: 2632 year: 2005 ident: WOS:000228957600002 article-title: New developments in the asymmetric Stetter reaction publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200500761 contributor: fullname: Christmann, M – volume: 20 start-page: 979 year: 1983 ident: WOS:A1983RE04100026 article-title: SYNTHESIS AND ACYLATING PROPERTIES OF 4,5-DIHYDRO-6H-1,3,4-OXADIAZIN-6-ONES publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY contributor: fullname: FARINA, C – volume: 107 start-page: 5606 year: 2007 ident: WOS:000251583300006 article-title: Organocatalysis by N-heterocyclic, carbenes publication-title: CHEMICAL REVIEWS doi: 10.1021/cr068372z contributor: fullname: Enders, D – volume: 6 start-page: 1108 year: 2008 ident: WOS:000253909000025 article-title: N-Heterocyclic carbene catalysed beta-lactam synthesis publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/b800857b contributor: fullname: Duguet, N – ident: e_1_2_3_35_2 doi: 10.1016/S0040-4039(01)98119-5 – ident: e_1_2_3_19_2 doi: 10.1021/jo00923a011 – ident: e_1_2_3_10_2 doi: 10.1002/ange.200500761 – ident: e_1_2_3_2_2 doi: 10.1055/sos-SD-023-00002 – ident: e_1_2_3_47_2 – ident: e_1_2_3_26_2 doi: 10.1021/ja00415a046 – ident: e_1_2_3_17_2 – ident: e_1_2_3_33_2 – ident: e_1_2_3_41_2 – ident: e_1_2_3_18_2 doi: 10.1016/S0040-4039(01)97825-6 – ident: e_1_2_3_38_2 doi: 10.1016/S0040-4039(01)97497-0 – ident: e_1_2_3_13_2 doi: 10.1021/ol702759b – ident: e_1_2_3_3_2 doi: 10.1002/ange.200500098 – start-page: 1759 year: 1983 ident: e_1_2_3_36_2 publication-title: J. Chem. Soc. Perkin Trans. 2 contributor: fullname: Bassman F. – ident: e_1_2_3_8_3 doi: 10.1002/anie.200603380 – ident: e_1_2_3_22_2 doi: 10.1016/B978-008044992-0.00808-7 – ident: e_1_2_3_39_2 doi: 10.1016/S0040-4039(01)86704-6 – ident: e_1_2_3_1_2 – ident: e_1_2_3_3_3 doi: 10.1002/anie.200500098 – ident: e_1_2_3_15_2 doi: 10.1021/jo801494f – ident: e_1_2_3_23_2 – ident: e_1_2_3_9_2 doi: 10.1002/ange.200502617 – ident: e_1_2_3_20_2 – ident: e_1_2_3_16_2 doi: 10.1002/chem.200801165 – ident: e_1_2_3_12_2 – ident: e_1_2_3_8_2 doi: 10.1002/ange.200603380 – ident: e_1_2_3_10_3 doi: 10.1002/anie.200500761 – ident: e_1_2_3_31_2 doi: 10.1039/B611091F – ident: e_1_2_3_34_2 – ident: e_1_2_3_27_2 doi: 10.1021/ja00415a047 – ident: e_1_2_3_7_2 doi: 10.1021/cr068372z – ident: e_1_2_3_9_3 doi: 10.1002/anie.200502617 – ident: e_1_2_3_45_2 doi: 10.1021/jo071247i – ident: e_1_2_3_29_2 – ident: e_1_2_3_32_3 doi: 10.1002/anie.200802439 – ident: e_1_2_3_24_2 doi: 10.1016/S0040-4039(01)98593-4 – ident: e_1_2_3_40_2 doi: 10.1016/S0040-4039(00)70256-5 – start-page: 2825 year: 2008 ident: e_1_2_3_44_2 publication-title: Synthesis contributor: fullname: He L. – ident: e_1_2_3_14_2 doi: 10.1039/b800857b – ident: e_1_2_3_32_2 doi: 10.1002/ange.200802439 – ident: e_1_2_3_11_2 doi: 10.1021/ar030050j – ident: e_1_2_3_6_2 – ident: e_1_2_3_42_2 doi: 10.1016/j.tetasy.2008.05.017 – ident: e_1_2_3_5_2 doi: 10.1016/S0040-4020(03)00491-5 – ident: e_1_2_3_4_2 doi: 10.1002/ejoc.200500452 – volume: 5 start-page: 406 year: 2007 ident: e_1_2_3_30_2 publication-title: Tetrahedron: Asymmetry contributor: fullname: Cativiela C. – ident: e_1_2_3_43_2 – ident: e_1_2_3_37_2 doi: 10.1016/S0040-4039(01)98120-1 – ident: e_1_2_3_46_2 – ident: e_1_2_3_28_2 doi: 10.1021/jo00186a026 – volume: 48 start-page: 781 year: 2005 ident: e_1_2_3_21_2 publication-title: Egypt. J. Chem. contributor: fullname: El‐Shenawy A. I. – ident: e_1_2_3_25_2 doi: 10.1002/jhet.5570200426 |
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| Snippet | Enantioselectivity switch: A catalytic enantioselective [4+2] cycloaddition reaction of alkylarylketenes with N‐aryl‐N′‐benzoyldiazenes or... |
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| StartPage | 192 |
| SubjectTerms | Aza Compounds - chemistry Benzene - chemistry carbenes Catalysis Chemistry Chemistry, Multidisciplinary Cyclization cycloaddition enantioselectivity Heterocyclic Compounds - chemistry ketenes Ketones - chemical synthesis Ketones - chemistry Methane - analogs & derivatives Methane - chemistry Molecular Structure Physical Sciences Science & Technology Stereoisomerism synthetic methods |
| Title | [4+2] Cycloaddition of Ketenes with N-Benzoyldiazenes Catalyzed by N-Heterocyclic Carbenes |
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