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Volumn 50, Issue 50, 2011, Pages 12075-12079

Catalytic [3+2] annulation of aminocyclopropanes for the enantiospecific synthesis of cyclopentylamines

Author keywords

cycloaddition; cyclopentylamines; diastereoselectivity; enantioselectivity; organocatalysis

Indexed keywords

BIOACTIVE COMPOUNDS; CYCLOPENTYLAMINES; DIASTEREO-SELECTIVITY; ENANTIOSPECIFIC SYNTHESIS; ENANTIOSPECIFICITY; ENOL ETHERS; ORGANOCATALYSIS; QUANTITATIVE YIELDS;

EID: 83455228768     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106255     Document Type: Article
Times cited : (148)

References (88)
  • 8
    • 64149121169 scopus 로고    scopus 로고
    • for some recent examples for the synthesis of cyclopentylamines, see
    • B. Heasley, Eur. J. Org. Chem. 2009, 1477; for some recent examples for the synthesis of cyclopentylamines, see
    • (2009) Eur. J. Org. Chem. , pp. 1477
    • Heasley, B.1
  • 85
    • 0027579802 scopus 로고
    • Deprotection of the silyl group without retro-aldol reaction could not be achieved so far.
    • O. Kanie, S. C. Crawley, M. M. Palcic, O. Hindsgaul, Carbohydr. Res. 1993, 243, 139. Deprotection of the silyl group without retro-aldol reaction could not be achieved so far.
    • (1993) Carbohydr. Res. , vol.243 , pp. 139
    • Kanie, O.1    Crawley, S.C.2    Palcic, M.M.3    Hindsgaul, O.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.