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Volumn 10, Issue 3, 2012, Pages 490-494

Organocatalytic asymmetric tandem condensation-intramolecular rearrangement-protonation: An approach to optically active α-amino thioester derivatives

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOSELECTIVE SYNTHESIS; GOOD YIELD; OPTICALLY ACTIVE; ORGANOCATALYTIC; SYNTHETIC BUILDING BLOCKS; THIOESTERS;

EID: 84055214134     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06623d     Document Type: Article
Times cited : (22)

References (97)
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    • E. Yamamoto A. Nagai A. Hamasaki M. Tokunaga Chem.-Eur. J. 2011 17 7178
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    • Yamamoto, E.1    Nagai, A.2    Hamasaki, A.3    Tokunaga, M.4
  • 44
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    • Enantioselective decarboxylation/re-protonation of malonate derivatives was reported previously by means of cinchona alkaloids, and represents a further example of metal-free enantioselective protonation, see
    • B. Wang F. Wu Y. Wang X. Liu L. Deng J. Am. Chem. Soc. 2007 129 768
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 768
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  • 51
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    • Selected reports of asymmetric catalyses using acid-base combined organic salt catalysts, see
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    • Lelais, G.1    MacMillan, D.W.C.2
  • 97
    • 38349135345 scopus 로고    scopus 로고
    • It is noteworthy that both quinine II and (-)-N-methylephedrine IV have the same configuration (1R,2S) as the amino alcohol moiety The mechanistic details and transition state structure of this new reaction, after further experimentation, will be published in due course
    • A. G. Doyle E. N. Jacobsen Chem. Rev. 2007 107 5713
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.