Hydroxyl- versus amide-directed cyclopropanation from the allylic position in 1-hydroxy-4-N-acyl-cyclopentenes under modified Simmons-Smith conditions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Stereochemistry of the cycloaddition reaction of methylcarbenoid of zinc to cyclic allylic alcohols
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4. Synthesis, Conformational Analysis, and Biological Activity of a Rigid Carbocyclic Analogue of 2′-Deoxy Aristeromycin Built on a Bicyclo[3.1.0]hexane Template
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1. 4.19 Methylene and Nonfunctionalized Alkylidene Transfer to Form Cyclopropanes;Comprehensive Organic Synthesis II;2014
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3. Chemo- and diastereoselective cyclopropanation of allylic amines and carbamates;Tetrahedron;2010-10
4. ChemInform Abstract: Hydroxyl- versus Amide-Directed Cyclopropanation from the Allylic Position in 1-Hydroxy-4-N-acyl-cyclopentenes under Modified Simmons- Smith Conditions.;ChemInform;2010-08-03
5. Total Syntheses of a Conformationally LockedNorth-Type Methanocarba Puromycin Analogue and a Dinucleotide Derivative;Chemistry - A European Journal;2009-06-15
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