Stereochemistry of sulfur-lithium and tin-lithium exchange reactions of functionalized cyclopropanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Optically active cyclopropanes
2. A Short, Efficient, Stereoselective Synthesis of Functionalized Cyclopropanes through the Cyclization ofN-Phenyl-3-phenylthio-2-(phenylthiomethyl)propanamide
3. Asymmetric synthesis of functionalized cyclopropanes via .beta.-lithiation-cyclization of N-monosubstituted 3-(phenylthio)-2-[(phenylthio)methyl]propanamides
4. Reductive Lithiation of Some Thioketals Using Lithium 1-(Dimethylamino)naphthalenide
5. A simple preparation of sulfur-stabilized cyclopropyl anions via reductive lithiation of cyclopropanone dithioketals.
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1. Lithium 1-(Dimethylamino)naphthalenide;Encyclopedia of Reagents for Organic Synthesis;2015-04-01
2. Organoalkali Chemistry;Organometallics in Synthesis: A Manual;2013-06-26
3. ChemInform Abstract: Stereochemistry of Sulfur - Lithium and Tin - Lithium Exchange Reactions of Functionalized Cyclopropanes.;ChemInform;2010-09-01
4. The superiority of properly prepared lithium 1-N,N-dimethylaminonaphthalenide (LDMAN) over other aromatic radical-anions for the generation of organolithiums by reductive lithiation;Tetrahedron Letters;2010-01
5. Synthetic Applications of Organic Germanium, Tin and Lead Compounds (Excluding R3MH);PATAI'S Chemistry of Functional Groups;2009-12-15
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