A convenient new procedure for the construction of highly substituted acetates. Reductive alkylation of α-cyano esters
- 3 November 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (44) , 7713-7716
- https://doi.org/10.1016/s0040-4039(97)10063-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Reductive cleavage of benzyl ethers with lithium naphthalenide. A convenient method for debenzylationTetrahedron Letters, 1997
- Carbon−Carbon Bond Formation from Small- and Medium-Ring Lactol Acetates via Radical and Oxonium Ion Intermediates. Synthesis of (±)-LaurenanThe Journal of Organic Chemistry, 1996
- Organolithium reagents by reductive decyanation of nitriles with lithium and a catalytic amount of 4,4′-Di-tert-butyl-biphenyl in a Barbier-Type reactionTetrahedron, 1994
- A new synthetic route to prostaglandinsTetrahedron Letters, 1986
- Geminal prostanoidsThe Journal of Organic Chemistry, 1980
- Alkylation and Acylation of Active Methylene Compounds Using 1,8-Diazabicyclo[5.4.0]undec-7-ene as a BaseBulletin of the Chemical Society of Japan, 1979
- Dialkylierung in Gegenwart von 1,8‐Diazabicyclo[5.4.0]undec‐7‐enEuropean Journal of Organic Chemistry, 1976
- Deconjugative alkylation of the enolate anion derived from ethyl crotonateTetrahedron Letters, 1973
- A convenient one flask procedure for ester alkylationTetrahedron Letters, 1973
- Reaction of lithium N-isopropylcyclohexylamide with esters. Method for the formation and alkylation of ester enolatesJournal of the American Chemical Society, 1971