Electronic control of stereoselectivity in the metal hydride reductions of 7-benzonorbornenones
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (23) , 2645-2648
- https://doi.org/10.1016/s0040-4039(00)84607-9
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- The synthesis of spiro[bicyclo[2.2.1]heptene-7,1′-cycloalkan]-2′-ones and related benzobicyclo[2.2.1]heptene derivativesCanadian Journal of Chemistry, 1976
- Simulation and evaluation of chemical synthesis. Congestion: a conformation-dependent function of steric environment at a reaction center. Application with torsional terms to stereoselectivity of nucleophilic additions to ketonesJournal of the American Chemical Society, 1976
- Orbital mixing ruleJournal of the American Chemical Society, 1976
- Stereochemistry of organometallic compound addition to ketonesChemical Reviews, 1975
- [1,3]-Sigmatropic rearrangement with retention of configuration forced upon the migrating groupJournal of the American Chemical Society, 1974
- Reactions of Norbornen-7-one with Organolithium ReagentsCanadian Journal of Chemistry, 1971
- Reactions of norbornyl-type ketones with diazomethaneThe Journal of Organic Chemistry, 1970
- Reactions of norbornen-7-one with Grignard reagentsCanadian Journal of Chemistry, 1970
- Rates of Reaction of Sodium Borohydride with Bicyclic Ketones. Steric Approach Control and Steric Departure Control in the Reactions of Rigid Bicyclic Systems1,2Journal of the American Chemical Society, 1966
- The Preparation and Stereospecific Rearrangement of Spiro[bicyclo[2.2.1]hept-2-en-anti-7,2'-oxacyclopropane]. The Effect of a Nonclassical Intermediate1The Journal of Organic Chemistry, 1963