Some observations regarding the stereochemical course of iminium ion reductions: An example of the size difference between sodium cyanoborohydride and sodium triacetoxyborohydride
- 1 May 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (20) , 5757-5770
- https://doi.org/10.1016/0040-4020(95)00253-5
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Clavepictines A and B: cytotoxic quinolizidines from the tunicate Clavelina pictaJournal of the American Chemical Society, 1991
- Total synthesis of (.+-.)-lythrancepine II and (.+-.)-lythrancepine IIIThe Journal of Organic Chemistry, 1987
- Intramolecular reactions of N-acyliminium intermediatesTetrahedron, 1985
- Synthetic applications of N-acylamino-1,3-dienes. 10. Importance of allylic interactions and stereoelectronic effects in dictating the steric course of the reaction of iminium ions with nucleophiles. An efficient total synthesis of (.+-.)-gephyrotoxinJournal of the American Chemical Society, 1983
- Preparation of primary amines and 2-azetidinones via N-(trimethylsilyl)iminesThe Journal of Organic Chemistry, 1983
- Stereochemistry of the Robinson-Schoepf reaction. A stereospecific total synthesis of the ladybug defense alkaloids precoccinelline and coccinellineJournal of the American Chemical Society, 1979
- Synthesis and diels-alder reactions of e-1-trimethylsilylbuta-1,3-dieneTetrahedron, 1979
- Studies on organophosphorus compounds XXI. the dimer of p‐methoxyphenylthionophosphine sulfide as thiation reagent. a new route to thiocarboxamidesBulletin des Sociétés Chimiques Belges, 1978
- A mild, general method for conversion of esters to amidesTetrahedron Letters, 1977
- A new method for the deoxygenation of secondary alcoholsJournal of the Chemical Society, Perkin Transactions 1, 1975