Affiliation:
1. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan
Abstract
Hydroalkoxylation of ynamide with propargylic alcohol, Saucy–Marbet rearrangement, and cyclization of the resultant 3,4-dienamide sequentially proceeds in a one-pot reaction under highly mild conditions to give fully substituted 2-aminofurans.
Funder
Japan Society for the Promotion of Science
Nagase Science Technology Foundation
Akiyama Life Science Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Cited by
7 articles.
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