Rearrangement de carbanion derivant d'allyl thioether
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. α-Alcoylation d'allyl-thioethers: couplage queue-a-queue d'unites isopreniques
2. Synthese du squalene par couplage queue a queue
3. Thermal cycloadditions of thiocarbonyl compounds to conjugated dienes
4. Cyclopropanes: The Cyclopropyl Carbanion1,2
5. Cyclopropanes. XIV. The Haller-Bauer Cleavage Reaction
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1. Stereoconvergent [1,2]- and [1,4]-Wittig Rearrangements of 2-Silyl-6-aryl-5,6-dihydropyrans: A Tale of Steric vs Electronic Regiocontrol of Divergent Pathways;The Journal of Organic Chemistry;2015-01-06
2. Cyclopentene Synthesis from 1,3-Dienes via Base-Induced Ring Contraction of 3,6-Dihydro-2H-thiopyrans: Studies on Diastereoselection and Mechanism;The Journal of Organic Chemistry;1996-01-01
3. The Thio-Wittig Rearrangement of Deprotonated Allyl Methyl Sulfide. A Gas-Phase Unimolecular Isomerization Probed with a Variable Temperature Flowing Afterglow-Triple Quadrupole Device;Journal of the American Chemical Society;1996-01-01
4. [2,3]1‐Thia‐Wittig Rearrangements Proceeding with Complete Inversion or with Partial Loss of Configuration at the Carbanionic Center;Chemische Berichte;1993-05
5. α-Alkylation of the Diels–Alder cycloadducts of the thioaldehyde, ethyl thioxoacetate;J. Chem. Soc., Perkin Trans. 1;1991
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