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Volumn 10, Issue 27, 2012, Pages 5289-5297

Enantioselective synthesis of gabapentin analogues via organocatalytic asymmetric Michael addition of α-branched aldehydes to β-nitroacrylates

Author keywords

[No Author keywords available]

Indexed keywords

BRANCHED ALDEHYDES; ENANTIOSELECTIVE SYNTHESIS; HIGH ENANTIOSELECTIVITY; HIGH YIELD; L-PHENYLALANINE; LITHIUM SALTS; MICHAEL ACCEPTORS; MICHAEL ADDITION REACTIONS; MICHAEL ADDITIONS; MICHAEL ADDUCTS; NITROESTERS; ONE STEP; ORGANOCATALYTIC; PRIMARY AMINO ACID; QUATERNARY CARBON;

EID: 84862838203     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25413a     Document Type: Article
Times cited : (40)

References (55)
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    • Dalpozzo, R.1    Bartoli, G.2    Bencivenni, G.3
  • 32
    • 0000220483 scopus 로고    scopus 로고
    • Reviews on organocatalysis using a primary amines
    • A. Alexakis O. Andrey Org. Lett. 2002 4 3611
    • (2002) Org. Lett. , vol.4 , pp. 3611
    • Alexakis, A.1    Andrey, O.2
  • 35
    • 49649083136 scopus 로고    scopus 로고
    • Asymmetric Michael addition of aldehydes to nitroalkenes with a primary amine catalyst
    • Y.-C. Chen Synlett 2008 1919
    • (2008) Synlett , pp. 1919
    • Chen, Y.-C.1
  • 53
    • 80054108505 scopus 로고    scopus 로고
    • The stereochemistry of 4k was determined to be syn by nOe analysis of amino acid 1c prepared from 4k as shown in the ESI.
    • M. Yoshida M. Narita S. Hara J. Org. Chem. 2011 76 8513
    • (2011) J. Org. Chem. , vol.76 , pp. 8513
    • Yoshida, M.1    Narita, M.2    Hara, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.