On the synthesis of aryl cyclopropanes from γ-benzenesulfonylalkyl tin derivatives and n-butyllithium.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Stereochemical outcome of benzyllithiums synthesis from selenides
2. Novel Synthesis of Arylcyclopropane Derivatives from α-Selenobenzyllithiums and Epoxides
3. Stereospecific cyclopropane-ring formation by 1,3-deoxymetalation of trimethyltin-substituted norbornyl mesylates
4. Deoxymetalation reactions. The concerted nature of 1,3-Deoxystannylation
5. Kinetics of cyclopropane formation by 1,3-deoxystannylation. A kinetic isotope effect as a probe for the mechanism of neighboring group participation
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1. 8.28 Reduction of SulfurCarbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon;Comprehensive Organic Synthesis II;2014
2. ChemInform Abstract: On the Synthesis of Aryl Cyclopropanes from γ- Benzenesulfonylalkyl Tin Derivatives and n-Butyllithium.;ChemInform;2010-08-20
3. Unprecedented dual reactivity of anhydrous potassium hydroxide in cascade cyclopropannelation/Haller–Bauer-scission/Grob-fragmentation reactions;Tetrahedron Letters;2010-08
4. Recent Advances in Synthesis of Cyclopropanes;PATAI'S Chemistry of Functional Groups;2009-12-15
5. n-Butyllithium;Encyclopedia of Reagents for Organic Synthesis;2009-09-15
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