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Volumn 21, Issue 6, 2002, Pages 591-604

Conjugate addition of amines to sugar derived olefinic esters: Synthesis of glycosylated amino esters as DNA topoisomerase-II inhibitors

Author keywords

Conjugate addition; DNA topoisomerase II; Glycosyl amino ester

Indexed keywords

AMINE; DNA TOPOISOMERASE INHIBITOR; ESTER DERIVATIVE; SUGAR;

EID: 0036921557     PISSN: 07328303     EISSN: None     Source Type: Journal    
DOI: 10.1081/CAR-120016857     Document Type: Article
Times cited : (24)

References (16)
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    • Intramolecular Michael addition of O-carbamates to α,β-unsaturated esters: A new diastereoselective amination in an acyclic system
    • Hirama, M.; Shigemoto, T.; Yamazaki, Y.; Ito, S. Intramolecular Michael addition of O-carbamates to α,β-unsaturated esters: A new diastereoselective amination in an acyclic system. J. Am. Chem. Soc. 1985, 107, 1797-1798.
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    • Intermolecular Michael addition of substituted amines to a sugar derived α,β-unsaturated ester: Synthesis of 1-deoxy-D-gluco and 1-ido homonojirimycin-1-deoxy-castanospermine and 1-deoxy-8a-epicastanospermine
    • Patil, N.T.; Tilekar, J.N.; Dhavale, D.D. Intermolecular Michael addition of substituted amines to a sugar derived α,β-unsaturated ester: Synthesis of 1-deoxy-D-gluco and 1-ido homonojirimycin-1-deoxy-castanospermine and 1-deoxy-8a-epicastanospermine. J. Org. Chem. 2001, 66, 1065.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.