The use of aminoiminomethanesulfinic acid (thiourea dioxide) under phase transfer conditions for generating organochalcogenate anions. Synthesis of sulfides, selenides and tellurides
- 1 November 1987
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 334 (3) , 329-340
- https://doi.org/10.1016/0022-328x(87)80095-5
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Synthesis of Diarylselenides and Diarylsulfides Under Phase Transfer ConditionsSynthetic Communications, 1986
- Alkaline hydrolysis of diaryl ditellurides under phase transfer conditions; synthesis of alkyl aryl telluridesJournal of Organometallic Chemistry, 1984
- Phase Transfer Catalyzed Melt Synthesis of Diaryl SulfidesSynthetic Communications, 1984
- Nucleophilic aromatic substitution reactions under phase-transfer conditions. Synthesis of alkyl aryl sulfides from isomeric dichlorobenzenes and thiolatesThe Journal of Organic Chemistry, 1983
- A Novel Synthesis of α and β -Pyran-naphthoquin one TetracyclicSynthetic Communications, 1982
- FACILE SUBSTITUTION REACTION BETWEEN NONACTIVATED ARYL IODIDES AND ARENETHIOLATES IN THE PRESENCE OF COPPER(I) IODIDEChemistry Letters, 1980
- An Iodine-Catalysed Reduction of Sulphoxides by Formamidinesulphinic AcidSynthesis, 1978
- The role of thiourea ss-dioxide in the reduction of steroidal ketonesTetrahedron Letters, 1975
- Reduction of Organic Sulfur Compounds by Formamidinesulfinic Acid under Phase-Transfer ConditionsSynthesis, 1975
- Reduction of organic compounds with thiourea dioxide. I. reduction of ketones to secondary alcoholsTetrahedron Letters, 1972