Diastereoselective chlorocyclofunctionalization of n-allylic trichloroacetamides : Synthesis of an analogue and potential precursor of RP49532
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (27) , 3871-3874
- https://doi.org/10.1016/s0040-4039(00)97492-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Première synthèse totale de la girollineTetrahedron, 1989
- Factors affecting the regioselection of allylic imidate iodocyclizationThe Journal of Organic Chemistry, 1986
- Practical multigram synthesis for 4(5)-vinylimidazoleThe Journal of Organic Chemistry, 1983
- Halonium-initiated cyclizations of allylic urethanes: stereo- and regioselectivity in functionalizing the olefinic bondJournal of the American Chemical Society, 1983
- Halocyclization of N-allylbenzamide derivatives. Effects of halogenating agent, alkene substitution, and mediumThe Journal of Organic Chemistry, 1978
- Attempted inhibition of histidine decarboxylase with .beta.-alkyl analogs of histidineJournal of Medicinal Chemistry, 1977
- A general method for the synthesis of amines by the rearrangement of allylic trichloroacetimidates. 1,3 Transposition of alcohol and amine functionsJournal of the American Chemical Society, 1976
- Rules for ring closureJournal of the Chemical Society, Chemical Communications, 1976
- Evidence against strongly-bridged bromonium ion intermediates in bromocyclization reactions of 2-butene derivativesTetrahedron Letters, 1974
- Neighboring group participation in polar bromination of styrene derivativesTetrahedron Letters, 1973