Retentive Stereospecificity in Deoxygenation of Epoxides with Sn–Al or Si–Al Reagents
- 1 May 1985
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 58 (5) , 1480-1483
- https://doi.org/10.1246/bcsj.58.1480
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Reformatsky Type Reaction with New Aluminium Reagents Containing Al–Sn or Al–Pb LinkageBulletin of the Chemical Society of Japan, 1984
- Reformatsky type reaction by means of Bu3SnA1et2 or Bu3Pba1et2Tetrahedron Letters, 1984
- Regioselective stannylmetalation of acetylenes in the presence of transition-metal catalystTetrahedron Letters, 1984
- Transition-metal-catalyzed silylmetalation of acetylenes and its application to the stereoselective synthesis of steroidal side chainsJournal of the American Chemical Society, 1983
- Some deoxygenation reactions with low-valent titanium (titanium trichloride/lithium tetrahydroaluminate)The Journal of Organic Chemistry, 1978
- Trimethylsilylpotassium. Deoxygenation of epoxides with inversion of stereochemistryJournal of the American Chemical Society, 1976
- Inversion of acyclic olefins by the phosphorus betaine method. Scope and limitationsJournal of the American Chemical Society, 1973
- Lower valent tungsten halides. New class of reagents for deoxygenation of organic moleculesJournal of the American Chemical Society, 1972
- Alkenes from halides and epoxides by reductive eliminations with CrII complexesTetrahedron, 1968
- Stereospecific Syntheses of Olefins from 1,2-Thionocarbonates and 1,2-Trithiocarbonates. trans-CyclohepteneJournal of the American Chemical Society, 1965