α-Lithio-δ-sultones: high preference for equatorial vs. axial lithium
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Protonation and methylation of conformationally fixed 2-lithio-1,3-dithianes. Some reactions of remarkable stereoselectivity
2. Stereochemical behavior of .alpha.-lithio sulfoxides (.alpha.-sulfinyl carbanions)
3. Solvent effect on the conformational preference of the carbanions derived from benzyl methyl sulfoxide
4. A new route to 5- and 6-membered ring sultones
5. Cyclohexylmetal compounds. III. Stereochemistry of some substitution reactions at the carbon-lithium bond
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1. Rearrangement and Cyclization of β-Mesyloxy Ketones. Synthesis of δ-Sultones;Bulletin des Sociétés Chimiques Belges;2010-09-01
2. Desulfurization of sultams with simultaneous methylenation;Tetrahedron Letters;2008-01
3. Chemistry of Sulfonate‐ and Sulfonamide‐Stabilized Carbanions − The CSIC Reactions;European Journal of Organic Chemistry;2003-09-16
4. Intramolecular Diels-Alder reaction of vinylsulfonates derived from hydroxyalkyl substituted 1,3-dienes and oxidative desulfurization of the resultant sultones;Tetrahedron;1995-01
5. Sulphonyl Carbanions;Sulphones in Organic Synthesis;1993
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