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Volumn 132, Issue 39, 2010, Pages 13608-13609

Asymmetric total synthesis of caribenol A

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC TOTAL SYNTHESIS; BIOMIMETIC OXIDATION; DIELS-ALDER;

EID: 77957296267     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja106585n     Document Type: Article
Times cited : (47)

References (30)
  • 17
    • 77957301458 scopus 로고    scopus 로고
    • 5 is prepared in 7 steps from the Roche ester; see the Supporting Information for details
    • - 5 is prepared in 7 steps from the Roche ester; see the Supporting Information for details.
  • 19
    • 77957312400 scopus 로고    scopus 로고
    • The rationale for the diastereoselective reduction is provided in the Supporting Information
    • The rationale for the diastereoselective reduction is provided in the Supporting Information.
  • 20
    • 77957317389 scopus 로고    scopus 로고
    • The stereochemistry at C3 in 13 could not be established at this stage, and its structure was eventually assigned on the basis of conversion of 2 to 1, which was compared with the reported data of caribenol A
    • The stereochemistry at C3 in 13 could not be established at this stage, and its structure was eventually assigned on the basis of conversion of 2 to 1, which was compared with the reported data of caribenol A.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.