Revisiting the 7-Phospanorbornene Family: New P-Alkyl Derivatives

被引:10
|
作者
Kovacs, Tamara [1 ]
Fueloep, Laura Sz. [1 ]
Mucsi, Zoltan [1 ]
Karaghiosoff, Konstantin [2 ]
Czugler, Matyas [1 ]
Keglevich, Gyoergy [1 ]
机构
[1] Budapest Univ Technol & Econ, Dept Organ Chem & Technol, H-1521 Budapest, Hungary
[2] Univ Munich, Dept Chem, D-81377 Munich, Germany
基金
匈牙利科学研究基金会;
关键词
LIGHT-MEDIATED FRAGMENTATION; VILLIGER TYPE OXIDATION; 7-(2,4,6-TRIALKYLPHENYL-)7-PHOSPHANORBORNENE 7-OXIDES; NMR PROPERTIES; COMPLEXES; PHOSPHORUS; OXIDES; 2,5-DIHYDRO-1H-PHOSPHOLE; PHOSPHINES; 1-OXIDE;
D O I
10.1002/hc.21265
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of 1-alkyl-3-methyl-2,5-dihydro-1H-phosphole oxides were converted to the corresponding phosphole oxides that, by the Diels-Alder reaction with N-maleimide derivatives or with another unit of phosphole oxide, yielded trapped phosphole oxides or phosphole oxide dimers, respectively, as new 7-phosphanorbornene 7-oxides. The stereostructures of three derivatives were evaluated by single crystal X-ray analysis. The regio- and stereospecific dimerization was studied by B3LYP/6-31G(d,p) quantum chemical calculations, whose results were in accord with syntheses. Novel mechanistic features were explored. The geometrical data obtained by single crystal X-ray analysis validated the results of quantum chemical calculations, as the deviation was less than 3%. (C) 2015 Wiley Periodicals, Inc.
引用
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页码:335 / 347
页数:13
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