Microwave-assisted tandem Wittig–intramolecular Diels–Alder cycloaddition. Product distribution and stereochemical assignment-Reference-Cited by-同舟云学术

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Microwave-assisted tandem Wittig–intramolecular Diels–Alder cycloaddition. Product distribution and stereochemical assignment

Published:2006-08 Issue:35 Volume:62 Page:8360-8372
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Wu Jinlong,Sun Lijie,Dai Wei-Min

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference146 articles.

1. The Diels–Alder Reaction: Selected Practical Methods,2002

2. Selected reviews on IMDA reaction, see:

3. Intramolecular Diels–Alder and Alder Ene Reactions;Taber,1984

4. The intramolecular Diels–Alder reaction: recent advances and synthetic applications

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2. Classical Example of Total Kinetic and Thermodynamic Control: The Diels–Alder Reaction between DMAD and Bis-furyl Dienes;The Journal of Organic Chemistry;2018-04-04

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4. Tandem-, Domino- and One-Pot Reactions Involving Wittig- and Horner-Wadsworth-Emmons Olefination;Alkenes;2018-02-07

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