New benzotriazole-based reagents for the phosphonylation of various N-, O-, and S-nucleophiles

被引：67
|
作者：
Panmand, Deepak S. [1 ]
Tiwari, Anand D. [1 ]
Panda, Siva S. [1 ]
Monbaliu, Jean-Christophe M. [1 ,2 ]
Beagle, Lucas K. [1 ]
Asiri, Abdullah M. [3 ,4 ]
Stevens, Christian V. [2 ]
Steel, Peter J. [5 ]
Hall, C. Dennis [1 ]
Katritzky, Alan R. [1 ,5 ]
机构：
[1] Univ Florida, Dept Chem, Ctr Heterocycl Cpds, Gainesville, FL 32611 USA
[2] Univ Ghent, Fac Biosci Engn, Dept Sustainable Organ Chem & Technol, B-9000 Ghent, Belgium
[3] King Abdulaziz Univ, Dept Chem, Jeddah 21589, Saudi Arabia
[4] King Abdulaziz Univ, Ctr Adv Mat Res CEAMR, Jeddah 21589, Saudi Arabia
[5] Univ Canterbury, Dept Chem, Christchurch 1, New Zealand
来源：
TETRAHEDRON LETTERS | 2014年 / 55卷 / 43期
关键词：
Benzotriazole; Phosphonylation; Conjugates; Nucleophile; Methodology; ORGANOPHOSPHORUS COMPOUNDS; QUANTITATIVE CHARACTERIZATION; DIALKYL CHLOROPHOSPHATES; CYCLOADDITION REACTIONS; ELECTROPHILICITY; REACTIVITY; EFFICIENT; ESTERS; ACIDS; PHOSPHONATES;
D O I：
10.1016/j.tetlet.2014.07.057
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Benzotriazole surrogates showing higher stabilities than the corresponding chlorophosphates, allow phosphonylation of a variety of N-, O-, and S-nucleophiles in good yields. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码：5898 / 5901
页数：4
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