Reductive allylation of pyrrole with allylboranes. Synthesis of trans- and cis-2,5-disubstituted pyrrolidines

DOI: 10.1007/BF02494816

Source and publish data:

Russian Chemical Bulletin p. 1696 - 1706 (1999)

Update date:2022-08-02

Topics:

Authors:

Bubnov Bubnov

Klimkina

Lavrinovich

Zykov Zykov

Ignatenko

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Article abstract of DOI:10.1007/BF02494816

Pyrrole undergoes reductive mono- and diallylation on successive treatment with β,γ-unsaturated organoboron derivatives (triallylborane, allyl(dipropyl)borane, and triprenylborane) and alcohols to give 2-allylated 3-pyrrolines and trans-2,5-diallylated py

Full text of DOI:10.1007/BF02494816

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