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Volumn 352, Issue 2-3, 2010, Pages 416-424

Asymmetric Michael addition reaction of 3-substituted oxindoles to nitroolefins catalyzed by a chiral alkyl-substituted thiourea catalyst

Author keywords

Bifunctional thioureas; Michael addition reaction; Nitroolefins; Organocatalysis; Oxindoles

Indexed keywords


EID: 77149143504     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.200900630     Document Type: Article
Times cited : (110)

References (65)
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    • and references cited therein
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    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 8666
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    • Other selected examples of catalytic asymmetric synthesis of oxindoles with quaternary carbon stereocenters: a S. Lee, J. F. Hartwig, J. Org. Chem. 2001, 66, 3402;
    • Other selected examples of catalytic asymmetric synthesis of oxindoles with quaternary carbon stereocenters: a) S. Lee, J. F. Hartwig, J. Org. Chem. 2001, 66, 3402;
  • 33
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    • E. P. Kündig, T. M. Seidel, Y.-X. Jia, G. Bernardinelli, Angew. Chem. 2007, 119, 8636; Angew. Chem. Int. Ed. 2007, 46, 8484;
    • d) E. P. Kündig, T. M. Seidel, Y.-X. Jia, G. Bernardinelli, Angew. Chem. 2007, 119, 8636; Angew. Chem. Int. Ed. 2007, 46, 8484;
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    • 7a,b]
    • 7a,b]
  • 45
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    • For leading examples of catalyst 1c: a T. Okino, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2003, 125, 12672;
    • For leading examples of catalyst 1c: a) T. Okino, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2003, 125, 12672;
  • 51
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    • For leading examples of catalyst 1e: a B. Vakulya, S. Varga, A. Csámpai, T. Soós, Org. Lett. 2005, 7, 1967;
    • For leading examples of catalyst 1e: a) B. Vakulya, S. Varga, A. Csámpai, T. Soós, Org. Lett. 2005, 7, 1967;
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    • For leading examples of catalyst 1f: a T.-Y. Liu, J. Long, B.-J. Li, L. Jiang, R. Li, Y. Wu, L.-S. Ding, Y.-C. Chen, Org. Biomol. Chem. 2006, 4, 2097;
    • For leading examples of catalyst 1f: a) T.-Y. Liu, J. Long, B.-J. Li, L. Jiang, R. Li, Y. Wu, L.-S. Ding, Y.-C. Chen, Org. Biomol. Chem. 2006, 4, 2097;
  • 63
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    • For leading example of catalyst 1g: Y. Sohtome, A. Tanatani, Y. Hashimoto, K. Nagasawa, Tetrahedron Lett. 2004, 45, 5589.
    • For leading example of catalyst 1g: Y. Sohtome, A. Tanatani, Y. Hashimoto, K. Nagasawa, Tetrahedron Lett. 2004, 45, 5589.
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    • Our catalyst 1b is also better than Takemotös catalyst 1c in the currently studied Michael addition reaction of 2b to nitrostyrene. See Scheme S1 in the Supporting Information
    • Our catalyst 1b is also better than "Takemotös catalyst" 1c in the currently studied Michael addition reaction of 2b to nitrostyrene. See Scheme S1 in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.