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Volumn 12, Issue 18, 2010, Pages 4050-4053

Kinetic resolution of racemic 2,3-allenoates by organocatalytic asymmetric 1,3-dipolar cycloaddition

Author keywords

[No Author keywords available]

Indexed keywords

ALLENOLIC ACID; NAPHTHALENE DERIVATIVE;

EID: 77956581197     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101544c     Document Type: Article
Times cited : (104)

References (49)
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    • Ma, S. Chem. Rev. 2005, 105, 2829
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    • For selected examples, see
    • For selected examples, see
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    • 76849091121 scopus 로고    scopus 로고
    • For gold-catalyzed cyclization of 2,3-allenoates, see:;;; J. Am. Chem. Soc. 2008, 130, 17642
    • Luö, B.; Fu, C.; Ma, S. Org. Biomol. Chem. 2010, 8, 274 For gold-catalyzed cyclization of 2,3-allenoates, see: Liu, L.-P.; Xu, B.; Mashuta, M. S.; Hammond, G. B. J. Am. Chem. Soc. 2008, 130, 17642
    • (2010) Org. Biomol. Chem. , vol.8 , pp. 274
    • Luö, B.1    Fu, C.2    Ma, S.3    Liu, L.-P.4    Xu, B.5    Mashuta, M.S.6    Hammond, G.B.7
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    • For selected excellent examples of synthesis of optically active 2,3-allenoates, see
    • For selected excellent examples of synthesis of optically active 2,3-allenoates, see
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    • 77956585855 scopus 로고    scopus 로고
    • For some reviews of the kinetic resolution, see
    • For some reviews of the kinetic resolution, see
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    • references cited therein. For selected examples of the kinetic resolution of 2,3-allenoic acid, see:; Chem. Commun. 2001, 441
    • Vedejs, E.; Jure, M. Angew. Chem., Int. Ed. 2005, 44, 3974 and references cited therein. For selected examples of the kinetic resolution of 2,3-allenoic acid, see: Ma, S.; Wu, S. Chem. Commun. 2001, 441
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 3974
    • Vedejs, E.1    Jure, M.2    Ma, S.3    Wu, S.4
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    • CCDC 776658. See the Supporting Information for details
    • CCDC 776658. See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.