Additions to bicyclic olefins—X
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Stereoselectivity of the Hydration of Representative Cyclic and Bicyclic Olefins by the New Oxymercuration-Demercuration Procedure
2. Solvomercuration-demercuration. I. Oxymercuration-demercuration of representative olefins in an aqueous system. Mild procedure for the Markovnikov hydration of the carbon-carbon double bond
3. STEREOCHEMISTRY OF THE HYDROXYMERCURATION OF ALKENES
4. Oxymercuration of strained olefins. Effect of neighboring groups
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4. Adjusting the Features of Active Metallocene Ziegler Systems fot Their Potential Use as Carbon–Carbon Coupling Catalysts in Organic Synthesis;Chemische Berichte;1997-02
5. Cyclization to Stereoisomeric Hexahydro-3,6-pentaleno[1,6-cd]pyran- 1(3H)-ones. A Model Study Explains the Preference for Trans Products;The Journal of Organic Chemistry;1996-01-01
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