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

页码：5898 / 5901

页数：4

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