Stereoselective Sequential Spirocyclopropanation/Cloke–Wilson Rearrangement Reactions for Synthesis of trans-β,γ-Disubstituted γ-Butyrolactones Using Alkylidene Meldrum’s Acid and Benzyl Halides
Author:
Affiliation:
1. College of Chemistry, Zhengzhou University, No. 100 Science Avenue, Zhengzhou 450001, P. R. China
Funder
Henan Province
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02978
Reference78 articles.
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3. Synthetic approaches towards structurally diverse γ-butyrolactone natural-product-like compounds
4. General Approach to 2,3-Dibenzyl-γ-butyrolactone Lignans: Application to the Total Synthesis of (±)-5′-Methoxyyatein, (±)-5′-Methoxyclusin, and (±)-4′-Hydroxycubebinone
5. Concise Total Synthesis of (−)-8-Epigrosheimin
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