期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 70, 期 16, 页码 6429-6440出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo050896w
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资金
- NIGMS NIH HHS [GM 35727] Funding Source: Medline
The brominative cyclization of diastereomeric beta-silyloxy tryptophan 'derivatives proceeded with divergent regiochemistry (C(2) or C(3) addition), depending on the relative stereochemistry of the silyloxy substituent. This lack of C(2) vs C(3) regiochemical predictability led to the development of a new approach, which featured Pummerer-type chemistry on an indole C(2) sulfoxide or sulfide substrate, for steering nucleophilic addition to C(3) of the indole. Extension of this transformation from carboxylate nucleophiles to carbon analogues such as allylsilane, silyl enol ether, and silyl ketene iminal bearing substrates led, to the formation of spirocyclic oxindole derivatives in good yields with complete regioselectivity for C(3) cyclization and with good diastereoselectivity where relevant.
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