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Volumn 126, Issue 38, 2004, Pages 11820-11825

α-alkylation of ketones by addition of zinc enamides to unactivated olefins

Author keywords

[No Author keywords available]

Indexed keywords

CARBON ELECTROPHILES; ISOBUTYLENES; REGIOSELECTIVITY; ZINC ENAMIDES;

EID: 4644314828     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0465193     Document Type: Article
Times cited : (42)

References (52)
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    • (1998) Metal-catalyzed Cross-coupling Reactions , pp. 271-337
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    • note
    • The reaction of a cyclohexanone imine with 1-octene showed the same range of the low diastereoselecitivity (data not reported). We are thus assuming that the poor diastereoselectivity in the reaction of the 3-pentanone imine is due to low selectivity of mutual face selection, but not to the E/Z isomerism of the zinc enamide intermediate.
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    • During the preparation of this article, two catalytic alkylation reactions of 1,3-dicarbonyl compounds with unactivated olefins were reported: (a) Yao, X.; Li, C.-J. J. Am. Chem. Soc. 2004, 126, 6884-6885.
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    • Yao, X.1    Li, C.-J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.