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The reactions of 4‐substituted‐7‐aminothieno‐[3,4‐d]pyridazines and 2‐methyl‐6‐aminothienopyridine‐5‐thione with electron‐poor olefins and acetylenes

The reactions of 4‐substituted‐7‐aminothieno‐[3,4‐d]pyridazines and... Cycloadditions of thienopyridazines and a thienopyridine with electron‐poor olefins and acetylenes as dienophiles are described. The nonisolable adducts undergo subsequent loss of hydrogen sulfide to give substituted phthalazines and substituted isoquinolines, respectively. © 1997 John Wiley & Sons, Inc. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

The reactions of 4‐substituted‐7‐aminothieno‐[3,4‐d]pyridazines and 2‐methyl‐6‐aminothienopyridine‐5‐thione with electron‐poor olefins and acetylenes

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References (9)

Publisher
Wiley
Copyright
Copyright © 1997 Wiley Subscription Services
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/(SICI)1098-1071(1997)8:1<29::AID-HC4>3.0.CO;2-Y
Publisher site
See Article on Publisher Site

Abstract

Cycloadditions of thienopyridazines and a thienopyridine with electron‐poor olefins and acetylenes as dienophiles are described. The nonisolable adducts undergo subsequent loss of hydrogen sulfide to give substituted phthalazines and substituted isoquinolines, respectively. © 1997 John Wiley & Sons, Inc.

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 1997

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