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Volumn 44, Issue 1, 2003, Pages 141-143

A sequential stereocontrolled cyclopropane ring formation and semi-pinacol rearrangement

Author keywords

[No Author keywords available]

Indexed keywords

2,3 EPOXY ALCOHOL; ALCOHOL; CYCLOPROPANE; UNCLASSIFIED DRUG;

EID: 0037213713     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02511-X     Document Type: Article
Times cited : (14)

References (19)
  • 9
    • 0012049119 scopus 로고    scopus 로고
    • 2 requires 224.1776.
    • 2 requires 224.1776.
  • 10
    • 0012019563 scopus 로고    scopus 로고
    • X-Ray data for 8 have been deposited at the Cambridge Crystallographic Data Centre, deposition number 195063.
    • X-Ray data for 8 have been deposited at the Cambridge Crystallographic Data Centre, deposition number 195063.
  • 12
    • 0012018837 scopus 로고    scopus 로고
    • Models suggest that a colinear alignment of the partial epoxide C-O bond and the p-orbital from the alkenic carbon atom, at the requisite distance for carbon-carbon bond formation, is more readily achievable in a transition state that leads to the seven-membered ring than in one that results in a six-membered ring.
    • Models suggest that a colinear alignment of the partial epoxide C-O bond and the p-orbital from the alkenic carbon atom, at the requisite distance for carbon-carbon bond formation, is more readily achievable in a transition state that leads to the seven-membered ring than in one that results in a six-membered ring.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.