A two-step synthesis of allylic syn 1,3-diols via an intramolecular oxa-Michael reaction followed by a modified Julia olefination
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Diastereoselective Synthesis of Protected syn 1,3-Diols: Preparation of the C16−C24 Portion of Dolabelides
2. Synthesis of functionalized Morita–Baylis–Hillman adducts by a conjugate addition–elimination sequence
3. Syntheses a l'aide de sulfones v(+)- methode de synthese generale de doubles liaisons.
4. Synthesis of protected syn 1,3-diols by intramolecular conjugate addition to vinyl sulfones
5. Condensation of β-hydroxy sulfones and vinyl sulfones with aldehydes and ketones using phenyllithium as base
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1. Trisubstituted Highly Activated Benzo[d]thiazol-2-yl-sulfone-Containing Olefins as Building Blocks in Organic Synthesis;The Journal of Organic Chemistry;2020-04-30
2. Novel Synthesis of Trisubstituted Olefins for the Preparation of the C16–C30 Fragment of Dolabelide C;Organic Letters;2018-12-27
3. Water-Compatible Synthesis of 2-Trifluoromethyl-1,3-Dioxanes;European Journal of Organic Chemistry;2018-11-20
4. Synthesis of 1,3-Diols by O-Nucleophile Additions to Activated Alkenes;Synthesis;2018-08-30
5. The Julia-Kocienski Olefination;Organic Reactions;2018-04-04
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