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Volumn 27, Issue 4, 2008, Pages 660-665

Stereoselective radical tandem cyclohydrostannation of optically active di-unsaturated esters of TADDOL

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ESTERS; ISOMERS; STEREOSELECTIVITY; UNSATURATED COMPOUNDS;

EID: 40549096387     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om700693p     Document Type: Article
Times cited : (15)

References (43)
  • 42
    • 40549113448 scopus 로고    scopus 로고
    • It has been reported (ref 2c) that substitution of a methyl group on the β-position of an acrylate ester reduces the rate of addition by nearly 100-fold
    • It has been reported (ref 2c) that substitution of a methyl group on the β-position of an acrylate ester reduces the rate of addition by nearly 100-fold.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.