Stereoselective Synthesis of α,β‐ trans 1‐Spiro‐β1‐lactones by Diels‐Alder Cycloaddition of 1,3‐Dienes to α1‐Methylene‐β1‐lactone and Their Decarboxylation by Pyrolysis to ( E )1‐Alkylidenecycloalkenes, a Convenient Olefination Method-Reference-Cited by-同舟云学术

Stereoselective Synthesis of α,β‐ trans 1‐Spiro‐β1‐lactones by Diels‐Alder Cycloaddition of 1,3‐Dienes to α1‐Methylene‐β1‐lactone and Their Decarboxylation by Pyrolysis to ( E )1‐Alkylidenecycloalkenes, a Convenient Olefination Method

Published:1993-06 Issue:6 Volume:126 Page:1481-1486
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Adam Walder¹,Salgado Victor Oswaldo Nava¹,Peters Eva‐Maria²,Peters Karl²,Schnering Hans Georg Von²

Affiliation:

1. Institut für Organische Chemie der Universität Würzburg, Am Hubland, W‐8700 Würzburg, F.R.G.

2. Max‐Planck‐Institut für Festkörperforschung, Heisenbergstraße 1, W‐7000 Stuttgart, F.R.G.

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19931260632

Reference32 articles.

1. Asymmetrische Diels-Alder- und En-Reaktionen in der Organischen Synthese

2. Asymmetric Diels-Alder and Ene Reactions in Organic Synthesis. New Synthetic Methods(48)

3. EPC Syntheses with C, C Bond Formation

4. N-substituted hydroxysuccinimides from (s)-malic acid as new reagents for asymmetric diels-alder additions to enoates

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