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Regioselectivity of Larock indole synthesis using functionalized alkynes


Bioscience, Biotechnology, and Biochemistry 72(8): 2092-2102
Regioselectivity of Larock indole synthesis using functionalized alkynes
Regioselectivity of Larock indole synthesis, a palladium-catalyzed heteroannulation between o-iodoaniline and internal acetylene, was estimated using acetylenes substituted with ester and/or Boc-protected amine at the homopropargylic position and with perbenzyl- and unprotected glucose. Low to moderate regioselectivities were observed in all the cases, indicating these functional groups do not exert good directing effects, in the Larock indole synthesis.

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Accession: 055445960

PMID: 18685222

DOI: 10.1271/bbb.80179



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