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Volumn 62, Issue 6, 2006, Pages 1102-1109

Stereochemical revision of communiols D and H through synthesis

Author keywords

Asymmetric dihydroxylation; Communiol; Dioxabicyclo 3.3.0 octane; Enantioselective synthesis; Podospora communis

Indexed keywords

ANTIINFECTIVE AGENT; COMMUNIOL A; COMMUNIOL B; COMMUNIOL C; COMMUNIOL D; COMMUNIOL H; UNCLASSIFIED DRUG;

EID: 29744440701     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.10.078     Document Type: Article
Times cited : (11)

References (17)
  • 15
    • 29744438062 scopus 로고    scopus 로고
    • note
    • 1H NMR) assignable to 7-H (communiol numbering) of each epimer (δ 4.48 for 10, and δ 4.37 for the cis-isomer). Comparison of the peak areas of the hemiacetalic proton signals of the epimeric mixture 13 (δ 4.95 and 5.25) indicated their ratio to be 2.8:1. The acetalic protons of 14 and its C3-epimer were observed at δ 5.70 and δ 5.58, respectively, which showed the ratio of them to be 6.3:1.
  • 17
    • 29744443358 scopus 로고    scopus 로고
    • note
    • 3 in our measurements as 7.24 and 77.0 ppm, respectively.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.