Methyl carbenoid addition to enol ethers carrying a chiral auxiliary. Stereocontrol of three chiral centers on cyclopropyl ether
- 14 January 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (3) , 367-368
- https://doi.org/10.1016/s0040-4039(00)74133-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Synthetic Approach for (+)-AfricanolChemistry Letters, 1990
- Regio- and Stereo-controlled Cyclopropanation of Unsaturated Enol EtherChemistry Letters, 1990
- Diastereo-differentiating cyclopropanation of a chiral enol ether: a simple method for the preparation of optically pure cyclopropyl ethersTetrahedron, 1990
- Diastereo-differentiating Simmons-Smith reaction using a new chiral auxiliaryTetrahedron Letters, 1989
- Diastereo-differentiating simmons-smith reaction using 2,4-pentanediol as a chiral auxiliaryTetrahedron Letters, 1988
- Stereochemical Studies. XXIX. Asymmetric Synthesis of 2-Alkylcyclohexanones via optically Active LithioenaminesCHEMICAL & PHARMACEUTICAL BULLETIN, 1974
- A novel synthesis of methylcyclopropanesTetrahedron, 1969
- Ring Enlargements. VIII. The Stereochemical Course of the Diazoalkanecarbonyl ReactionJournal of the American Chemical Society, 1962