Preparation and Diels-Alder Reaction of a Highly Nucleophilic Diene:trans-1-Methoxy-3-Trimethylsiloxy-1,3-Butadiene and 5β-Methoxycyclohexan-1-One-3β,4β-Dicarboxylic Acid Anhydride-Reference-Cited by-同舟云学术

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Preparation and Diels-Alder Reaction of a Highly Nucleophilic Diene:trans-1-Methoxy-3-Trimethylsiloxy-1,3-Butadiene and 5β-Methoxycyclohexan-1-One-3β,4β-Dicarboxylic Acid Anhydride

Published:2003-04-28 Issue: Volume: Page:147-147
ISSN:
Container-title:Organic Syntheses
language:
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Author:

Danishefsky Samuel¹²,Kitahara Takeshi¹,Schuda Paul F.¹

Affiliation:

1. University of Pittsburgh; Department of Chemistry; Pittsburgh PA 15260

2. Yale University; Department of Chemistry; New Haven CT 06520

Publisher

John Wiley & Sons, Inc.

Reference5 articles.

1. Useful diene for the Diels-Alder reaction

2. A new stereoselective synthesis of dl-pumiliotoxin C using novel 1,3-bis(trimethylsilyloxy)-1,3-dienes

3. Diels-Alder adducts of acetoxy-1,3-dienes and p-benzoquinone

4. Diels-Alder route to cis-fused .DELTA.1-3-octalones

5. A remarkable epoxide opening. An expeditious synthesis of vernolepin and vernomenin

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