Guanidines: from classical approaches to efficient catalytic syntheses

被引:184
作者
Alonso-Moreno, Carlos [1 ]
Antinolo, Antonio [2 ]
Carrillo-Hermosilla, Fernando [2 ]
Otero, Antonio [2 ]
机构
[1] Univ Castilla La Mancha, Fac Farm, Dept Quim Inorgan Organ & Bioquim, Albacete 02071, Spain
[2] Univ Castilla La Mancha, Fac Ciencias & Tecnol Quim, Dept Quim Inorgan Organ & Bioquim, E-13071 Ciudad Real, Spain
关键词
RING-OPENING POLYMERIZATION; SOLID-PHASE SYNTHESIS; SUBSTITUTED GUANIDINES; N-H; EPSILON-CAPROLACTONE; LIGANDS SYNTHESIS; SECONDARY-AMINES; METAL-COMPLEXES; M(NME2)(5) M; C-C;
D O I
10.1039/c4cs00013g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
From organosuperbases capable of base-catalyzing organic reactions, through versatile 'ligand-sets' for use in coordination chemistry, to fundamental entities in medicinal chemistry, guanidines are amongst the most interesting, attractive, valuable, and versatile organic molecules. Since the discovery of these compounds, synthetic chemists have developed new methodologies that are mainly based on multi-step and stoichiometric reactions. Despite the fact that these methodologies are still being used by the interested scientific and industrial communities, drawbacks such as the poor availability of precursors, low yields, and use and production of undesirable substances highlight the need for safe, simple and efficient syntheses of these entities. This review focuses on the metal-mediated catalytic addition of amines to carbodiimides as an atom-economical alternative to the classical synthesis.
引用
收藏
页码:3406 / 3425
页数:20
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