Abstract
Stereoselective reduction of a triple C-C bond and chemoselective transformation of an azide function into amino group have been employed in the synthesis of straight-chain primary E and Z allylic amines from alk-2-yn-1-ols.
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, 1998 - Issue 7
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Related Research Data
Allylic azides: synthesis, reactivity, and the Winstein rearrangement.
Source:
Royal Society of Chemistry (RSC)
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