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Volumn 79, Issue 2, 2014, Pages 783-789

Regio- and stereocontrolled access to ?-boronated unsaturated amino esters and derivatives from (z)-alkenyl 1,2-bis(boronates)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; ESTERS;

EID: 84896773261     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo402237t     Document Type: Article
Times cited : (18)

References (52)
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    • 84896800703 scopus 로고    scopus 로고
    • Boronic acids: Preparation, Applications in Organic Synthesis and Medicine, 2nd ed. Hall,D. G. Wiley VCH: Weinheim, Germany
    • Boronic acids: Preparation, Applications in Organic Synthesis and Medicine, 2nd ed.; Hall, D. G., Ed.; Wiley VCH: Weinheim, Germany, 2011.
  • 8
    • 51649120855 scopus 로고    scopus 로고
    • For intramolecular versions, see
    • For intramolecular versions, see: (a) Carson, M. W.; Giese, M. W.; Coghlan, M. J. Org. Lett. 2008, 10, 2701.
    • (2008) Org. Lett. , Issue.10 , pp. 2701
    • Carson, M.1    Giese, M.2    Coghlan, M.3
  • 18
    • 77958034343 scopus 로고    scopus 로고
    • For recent reviews on the Petasis three-component coupling reaction, see:
    • For recent reviews on the Petasis three-component coupling reaction, see: (a) Candeias, N. R.; Montalbano, F.; Cal, P. M. S. D.; Gois, P. M. P. Chem. Rev. 2010, 110, 6169.
    • (2010) Chem. Rev. , Issue.110 , pp. 6169
    • Candeias, N.1    Montalbano, F.2    Cal, D.P.M.S.3    Gois, P.P.M.4
  • 47
    • 84867709245 scopus 로고    scopus 로고
    • For Some Recent Examples Of This One-pot Process See
    • For some recent examples of this one-pot process, see: (a) Akula, H. K.; Lakshman, M. K. J. Org. Chem. 2012, 77, 8896.
    • (2012) J. Org. Chem. , vol.77 , pp. 8896
    • Akula, H.K.1    Lakshman, M.K.2
  • 51
    • 33749583652 scopus 로고
    • Because of its explosiveness toxicity diazomethane was directly generated in diethyl ether used without further purification after simple decantation
    • Because of its explosiveness and toxicity, diazomethane was directly generated in diethyl ether and used without further purification after simple decantation, see: Arndt, F. Org. Synth. 1935, 15, 3;
    • (1935) Org. Synth. , vol.15 , pp. 3
    • Arndt, F.1
  • 52
    • 0004235357 scopus 로고
    • Org. Synth. 1943, II, 165.
    • (1943) Org. Synth. , vol.2 , pp. 165


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.