Microwave-assisted synthesis of α-aminophosphonates with sterically demanding α-aryl substituents

被引:9
作者
Hudson, Harry R. [1 ]
Tajti, Adam [2 ]
Balint, Erika [2 ]
Czugler, Matyas [2 ]
Karaghiosoff, Konstantin [3 ]
Keglevich, Gyorgy [2 ]
机构
[1] London Metropolitan Univ, Fac Life Sci & Comp, London, England
[2] Budapest Univ Technol & Econ, Dept Organ Chem & Technol, H-1521 Budapest, Hungary
[3] Ludwig Maximilians Univ Munchen, Dept Chem, Munich, Germany
关键词
alpha-Aminophosphonate; crystal structure; C - H delta+ center dot center dot center dot H delta+ - C bonds; Kabachnik-fields reaction; microwave; X-ray diffraction; KABACHNIK-FIELDS REACTION; DOT-H DISTANCES; DERIVATIVES; SOLVENT; BONDS; ACIDS; DFT;
D O I
10.1080/00397911.2019.1679186
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of N-benzhydryl protected alpha-aminophosphonates with alpha-phenyl, alpha-(1-naphtyl), alpha-(9-anthryl) or alpha-(1-pyrenyl) substituents was synthesized by the Kabachnik-Fields condensation of diphenylmethylamine (benzhydrylamine), the corresponding aryl aldehyde and a dialkyl phosphite under MW irradiation. X-ray studies performed at low temperatures for a few of these alpha-aminophosphonates confirmed the presence of unusually short intramolecular C-alpha-H delta+ center dot center dot center dot H delta+-C-peri contacts. [GRAPHICS] .
引用
收藏
页码:1446 / 1455
页数:10
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