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Volumn 65, Issue 4, 2000, Pages 490-510

Studies toward an asymmetric synthesis of CP-263,114 and CP-225,917

Author keywords

Allylic oxidation; Birch reduction; Claisen rearrangement; CP compounds; Dihydroxylation; Iodolactonization; Total synthesis

Indexed keywords


EID: 0034413231     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20000490     Document Type: Article
Times cited : (21)

References (58)
  • 58
    • 2142858450 scopus 로고
    • The Kakisawa method is based on the adoption of an idealized conformation in which the carbinyl proton, ester carbonyl, and trifluoromethyl groups of the MTPA ester are in the same plane: Ohtani I., Kusumi T., Kashman Y., Kakisawa H.: J. Am. Chem. Soc. 1991, 113, 4092.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.