Synthesis of 3,5-disubstituted pyridazines by regioselective [4+2] cycloadditions with ethynyltributyltin and subsequent replacement of the organotin substituent-Reference-Cited by-同舟云学术

Synthesis of 3,5-disubstituted pyridazines by regioselective [4+2] cycloadditions with ethynyltributyltin and subsequent replacement of the organotin substituent

Published:1998-04 Issue:17 Volume:54 Page:4297-4312
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Sauer Jürgen,Heldmann Dieter K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Synthesis of metallated (metal = Si, Ge, Sn) pyridazines by cycloaddition of metal substituted alkynes to 1,2,4,5-tetrazine

2. Ein Beitrag zur Reaktivität und Regiochemie ausgewählter Diazadiene in der inversen [4+2]-Cycloaddition;Hierstetter,1994

3. Ab initio quantum-mechanical and experimental mechanistic studies of Diels-Alder reactions between unsubstituted and phenyl-substituted acetylenes and 1,2,4,5-tetrazines

4. Synthese von 3‐Phenyl‐5‐silylpyridazinen durch regioselektive [4 + 2]‐Cycloadditionen

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