The Journal of organic chemistry

Metal-Catalyzed Reaction Of Indoline Diazoamides Possessing a C-2 CH2X Substituent: Site-Selectivity, Diastereoselectivity, and Chemoselectivity

AGH Wee, J Slobodian

Index: Wee, Andrew G. H.; Slobodian Journal of Organic Chemistry, 1996 , vol. 61, # 8 p. 2897 - 2900

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Citation Number: 26

Abstract

Results The diazoamides 9 and 10 were prepared from the indoline alcohols 5-7, which were readily obtained from the known3 2-indolecarboxylates 4 (R) H or OMe)(Scheme 1). Alcohols 5-7 were converted via standard functional group manipulations (supporting

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