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Volumn 18, Issue 3, 2004, Pages 209-214

A promising enantioselective Diels-Alder dienophile by computer-assisted rational design: 2,5-diphenyl-1-vinyl-borolane

Author keywords

Asymmetric synthesis; Boranes; Cycloadditions; Density functional calculations; Ligand design

Indexed keywords

BORON COMPOUNDS; CYCLOADDITION; ENANTIOSELECTIVITY; HYDRIDES;

EID: 4043087807     PISSN: 0920654X     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:JCAM.0000035200.30340.41     Document Type: Article
Times cited : (9)

References (38)
  • 6
    • 30444444851 scopus 로고
    • There are a few examples of highly selective cycloadditions of vinylboronates, but all these process make use of either an additional chiral catalyst or reagents having an extra stereo-center or chiral auxillary not directly attached to the boronate moiety
    • For instance, see
    • There are a few examples of highly selective cycloadditions of vinylboronates, but all these process make use of either an additional chiral catalyst or reagents having an extra stereo-center or chiral auxillary not directly attached to the boronate moiety. For instance, see: Narasaka, K. and Yamamoto, I. Tetrahedron, 48 (1992) 5743;
    • (1992) Tetrahedron , vol.48 , pp. 5743
    • Narasaka, K.1    Yamamoto, I.2
  • 34
    • 4043129439 scopus 로고    scopus 로고
    • Jaguar 4.2, Schrodinger, Inc., Portland, Oregon
    • Jaguar 4.2, Schrodinger, Inc., Portland, Oregon, 2000.
    • (2000)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.