메뉴 건너뛰기




Volumn 49, Issue 5, 2008, Pages 816-819

Synthesis of the C1-C12 fragment of the tedanolides. Selective hydroboration-protonation of allylic alcohol approach

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; CYTOTOXIC AGENT; TEDANOLIDE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 37649012456     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.11.181     Document Type: Article
Times cited : (7)

References (36)
  • 3
    • 34848898191 scopus 로고    scopus 로고
    • Total syntheses of tedanolide:
    • Total syntheses of tedanolide:. Smith III A.B., and Lee D. J. Am. Chem. Soc. 129 (2007) 10957
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 10957
    • Smith III, A.B.1    Lee, D.2
  • 36
    • 37649008874 scopus 로고    scopus 로고
    • note
    • Attempted hydroboration of the corresponding trimethylsilyl or triethylsilyl ether of alcohol 11 under normal conditions gave back only the starting materials presumably due to increased steric hindrance around the alkene (possibly due to lack of coordination of the alcohol to the ether as shown in A which holds the molecule in a conformation favorable for reduction).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.