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Volumn 64, Issue 21, 2008, Pages 4700-4710

A synthesis of (aR,7S)-(-)-N-acetylcolchinol and its conjugate with a cyclic RGD peptide

Author keywords

Asymmetric reduction; Biaryl; Colchicine; RGD peptide; Suzuki Miyaura cross coupling

Indexed keywords

BENZENE DERIVATIVE; COLCHINOL; LEWIS ACID; LITHIUM DERIVATIVE; N ACETYLCOLCHINOL ARGINYLGLYCYLASPARTIC ACID CONJUGATE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 42449137851     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.130     Document Type: Article
Times cited : (37)

References (71)
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    • The induction of mitotic arrest by colchicine was first recorded in 1889 by B. Pernice, a Sicilian pathologist active in Palermo from 1884 to 1906. Owing to limited dissemination, Pernice's pioneering contribution was not appreciated until 1949 (. Eigsti O.J., Dustin P., and Gay-Winn N. Science (1949) 692 )
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    • In a previous paper (Ref. 19), we erroneously described the stereochemistry of (-)-N-acetylcolchinol as (aS,7S). It should be (aR,7S). This common mistake was rectified in 1998:
    • In a previous paper (Ref. 19), we erroneously described the stereochemistry of (-)-N-acetylcolchinol as (aS,7S). It should be (aR,7S). This common mistake was rectified in 1998:. Berg U., and Bladh H. Helv. Chim. Acta 82 (1998) 323-325
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    • note
    • Banwell (Ref. 36) and Wulff (Ref. 39) both recorded the need for stoichiometric amounts of the CBS oxazaborolidine catalyst to accomplish related asymmetric reductions.
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    • note
    • 2 has been used in a synthesis of allocolchicine by Wulff and co-workers (see Ref. 39).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.