Stereoselective Alkylations in Rigid Systems. Effect of Remote Substituents on π-Facial Additions to Lactam Enolates. Stereoelectronic and Steric Effects
- 18 July 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (30) , 7429-7438
- https://doi.org/10.1021/ja980614s
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Origin of Stereochemistry in Simple Pyrrolidinone Enolate AlkylationsJournal of the American Chemical Society, 1997
- Chiral bicyclic lactams: useful precursors and templates for asymmetric syntheses1Chemical Communications, 1997
- Chiral Bicyclic Lactams. A New Study on Facial AlkylationThe Journal of Organic Chemistry, 1996
- Solvation-controlled diastereofacial selectivity in alkylations of bicyclic lactam enolatesJournal of the American Chemical Society, 1990
- Some observations on the validity and generality of the "Cieplak stereoelectronic effect"The Journal of Organic Chemistry, 1989
- Conversion of L-pyroglutamic acid to 4-alkyl-substituted L-prolines. The synthesis of trans-4-cyclohexyl-L-prolineThe Journal of Organic Chemistry, 1986
- Asymmetric synthesis of quaternary carbon centersJournal of the American Chemical Society, 1984
- Stereochemistry of nucleophilic addition to cyclohexanone. The importance of two-electron stabilizing interactionsJournal of the American Chemical Society, 1981
- Structural Studies of Crystalline EnaminesHelvetica Chimica Acta, 1978
- Synthetic applications of trimethylsilyl cyanide. Efficient synthesis of .beta.-aminomethyl alcoholsThe Journal of Organic Chemistry, 1974