Chiral dipole-stabilized anions: experiment and theory in benzylic and allylic systems. Stereoselective deprotonations, pyramidal inversions, and stereoselective alkylations of lithiated (tetrahydroisoquinolyl)oxazolines
- 1 March 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 111 (6) , 2211-2217
- https://doi.org/10.1021/ja00188a040
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Chiral dipole-stabilized anions: experiment and theory in nonbenzylic systems. 100 Percent stereoselective deprotonation and two-electron versus single-electron transfer in the chemistry of lithium and copper piperidinooxazolinesThe Journal of Organic Chemistry, 1989
- Asymmetric synthesis of isoquinoline alkaloidsTetrahedron, 1987
- Asymmetric synthesis of 2-alkyl pyrrolidines and piperidines. Synthesis of (+)-metazocineJournal of the American Chemical Society, 1985