This article is cited in 8 scientific papers (total in 8 papers)
2,4,4,6-Tetrabromocyclohexa-2,5-dienone in the presence of triphenylphosphine as a regiospecific and stereoselective reagent for the nucleophilic substitution of bromine for hydroxyl
Abstract:
A highly reactive, regio- and stereo-specific reagent, a 2,4,4,6-tetrabromocyclohexa-2,5-dienone–triphenylphosphine complex, has been used for the first time in the nucleophilic substitution of bromine for hydroxyl in alcohols.
Document Type:
Article
Language: English
Citation:
E. D. Matveeva, T. A. Podrugina, N. S. Zefirov, “2,4,4,6-Tetrabromocyclohexa-2,5-dienone in the presence of triphenylphosphine as a regiospecific and stereoselective reagent for the nucleophilic substitution of bromine for hydroxyl”, Mendeleev Commun., 8:1 (1998), 21–23
Linking options:
https://www.mathnet.ru/eng/mendc4637
https://www.mathnet.ru/eng/mendc/v8/i1/p21
This publication is cited in the following 8 articles:
Naruti Longkumer, Kikoleho Richa, Rituparna Karmaker, Basanta Singha, Upasana Bora Sinha, “Facile Green Synthesis of Bromoaniline Molecules: An Experimental and
Computational Insight into their Antifungal Behaviour”, Asian J. Chem., 34:12 (2022), 3115
Indranirekha Saikia, Arun Jyoti Borah, Prodeep Phukan, “Use of Bromine and Bromo-Organic Compounds in Organic Synthesis”, Chem. Rev., 116:12 (2016), 6837
Henri A. van Kalkeren, Floris L. van Delft, Floris P. J. T. Rutjes, “Catalytic Appel reactions”, Pure and Applied Chemistry, 85:4 (2012), 817
Henri A. van Kalkeren, Stefan H. A. M. Leenders, C. Rianne A. Hommersom, Floris P. J. T. Rutjes, Floris L. van Delft, “In Situ Phosphine Oxide Reduction: A Catalytic Appel Reaction”, Chemistry A European J, 17:40 (2011), 11290
Elena B. Averina, Rashad R. Karimov, Kseniya N. Sedenkova, Yurii K. Grishin, Tamara S. Kuznetzova, Nikolai S. Zefirov, “Carbenoid rearrangement of gem-dihalogenospiropentanes”, Tetrahedron, 62:37 (2006), 8814
E. D. Matveeva, T. A. Podrugina, N. G. Sandakova, N. S. Zefirov, “Triphenylphosphine-2,4,4,6-tetrabromo-2,5-cyclohexadienone complex as a reagent for preparation of carboxylic acid bromides”, Russ J Org Chem, 40:10 (2004), 1469
E. D. Matveeva, T. A. Podrugina, E. V. Tishkovskaya, N. S. Zefirov, “2,4,4,6-Tetrabromocyclohexa-2,5-dienone in the presence of triphenylphosphine as a specific reagent for nucleophilic substitution in cyanohydrins”, Mendeleev Commun., 13:6 (2003), 260–262
E. D. MATVEEVA, T. A. PODRUGINA, N. S. ZEFIROV, “ChemInform Abstract: 2,4,4,6‐Tetrabromocyclohexa‐2,5‐dienone in the Presence of Triphenylphosphine as a Regiospecific and Stereoselective Reagent for the Nucleophilic Substitution of Bromine for Hydroxyl.”, ChemInform, 29:30 (1998)
Contact us: