2-(Trimethylsilyloxy)furan as a Dianion Equivalent: A Two-Step Synthesis of Functionalized Spirocyclic Butenolides
Author:
Affiliation:
1. Université catholique de Louvain, Département de Chimie, 1 Place Louis Pasteur, B-1348 Louvain-la-Neuve, Belgium
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol061284g
Reference25 articles.
1. Synthesis of Spirocyclic Butenolides by Ring Closing Metathesis
2. Enantioselective Synthesis of a Highly Preorganised 2′-Deoxy-spiro-nucleoside
3. Efficient synthesis of α,β-unsaturated γ-lactones linked to sugars
4. 1-Oxaspiro[4.4]nonan-6-ones. Synthetic Access via Oxonium Ion Technology, Optical Resolution, and Conversion into Enantiopure Spirocyclic α,β-Butenolides
5. Efficient synthesis of spirolactones from cyclic anhydrides via an allylation/alkylation-RCM sequence
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