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A FISCHER INDOLIZATION STRATEGY TOWARD THE TOTAL SYNTHESIS OF (-)-GONIOMITINE.


ABSTRACT: A Fischer indolization strategy toward the core of (-)-goniomitine is reported. Initial investigations into the Pd-catalyzed asymmetric allylic alkylation of dihydropyrido[1,2-a]indolone (DHPI) substrates are also discussed.

SUBMITTER: Pritchett BP 

PROVIDER: S-EPMC5502790 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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A FISCHER INDOLIZATION STRATEGY TOWARD THE TOTAL SYNTHESIS OF (-)-GONIOMITINE.

Pritchett Beau P BP   Kikuchi Jun J   Numajiri Yoshitaka Y   Stoltz Brian M BM  

Heterocycles 20170215 2


A Fischer indolization strategy toward the core of (-)-goniomitine is reported. Initial investigations into the Pd-catalyzed asymmetric allylic alkylation of dihydropyrido[1,2-<i>a</i>]indolone (DHPI) substrates are also discussed. ...[more]

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