The use of o-nitroarylacetonitriles as carbon acid participants in the mitsunobu reaction
- 1 December 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (49) , 7195-7198
- https://doi.org/10.1016/0040-4039(91)80474-k
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- 3-(1,2,5,6-Tetrahydropyrid-4-yl)pyrrolo[3,2-b]pyrid-5-one: a potent and selective serotonin (5-HT1*) agonist and rotationally restricted phenolic analog of 5-methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl)indoleJournal of Medicinal Chemistry, 1990
- The Synthesis of a Rotationally Restricted Phenolic Analog of 5-Methoxy-3-(1,2,5,6-tetrahydropyrid-4-yl)indole (RU-24,969)HETEROCYCLES, 1990
- Reactions of organic anions, 147. Simple and general synthesis of hydroxy‐ and methoxyindoles via vicarious nucleophilic substitution of hydrogenEuropean Journal of Organic Chemistry, 1988
- The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural ProductsSynthesis, 1981
- Intermolecular dehydration between alcohols and active hydrogen compounds by means of diethyl azodicarboxylate and triphenylphosphineTetrahedron Letters, 1972