Rearrangements of the [2+2]-cycloadducts of DDQ and 2-ethynylpyrroles-Reference-Cited by-同舟云学术

Rearrangements of the [2+2]-cycloadducts of DDQ and 2-ethynylpyrroles

Published:2010-09 Issue:38 Volume:51 Page:5028-5031
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Trofimov Boris A.,Sobenina Lyubov N.,Stepanova Zinaida V.,Ushakov Igor A.,Mikhaleva Albina I.,Tomilin Denis N.,Kazheva Olga N.,Alexandrov Grigorii G.,Chekhlov Anatolii N.,Dyachenko Oleg A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Facile [2+2] Cycloaddition of DDQ to an Alkyne: Synthesis of Pyrrolyl- and Indolylbicyclo[4.2.0]octadienes from C-Ethynylpyrroles or C-Ethynylindoles

2. Ethynylation of pyrroles with 1-acyl-2-bromoacetylenes on alumina: a formal ‘inverse Sonogashira coupling’

3. Chemo- and regioselective ethynylation of 4,5,6,7-tetrahydroindoles with ethyl 3-halo-2-propynoates

4. Synthesis and solvolytic rearrangement of 1-methoxybicyclo[4.2.0]octa-3,7-diene-2,5-diones

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