In:
Advanced Synthesis & Catalysis, Wiley, Vol. 358, No. 2 ( 2016-01-21), p. 303-313
Abstract:
Palladium catalyzed conversion of 1‐(2‐aminophenyl)‐propargyl alcohols to 3‐alkynyl quinolines is realized via a cascade that involves aminopalladation, oxidative coupling with alkynes and dehydration. The method is shown to have a broad substrate scope with respect to propargyl alcohols as well as alkynes. Vinyl ketones as coupling partners in the same reaction afforded 3‐alkenyl quinolines with equal ease. magnified image
Type of Medium:
Online Resource
ISSN:
1615-4150
,
1615-4169
DOI:
10.1002/adsc.201500805
Language:
English
Publisher:
Wiley
Publication Date:
2016
detail.hit.zdb_id:
2041384-1
detail.hit.zdb_id:
2033084-4
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