Add to ORKGBy gas-phase pyrolysis over a solid base the title compound has been prepared as a 1:1 mixture with its hydration product and characterised spectroscopically; the hindered C=P double bond is surprisingly unreactive. (C) 1999 Elsevier Science Ltd. All rights reserved.</p
Contrary to a previous report, the sulfurisation of phosphorus(III) derivatives by 3-amino-1,2,4-dit...
In solution the PCy3/B(C6F5)3 pair is rapidly deactivated by nucleophilic aromatic substitution. In ...
Caution! Decomposition of excess PCl3 (step A) should be carried out carefully in a fume-hood becaus...
Hoge B, Garcia P, Willner H, Oberhammer H. Bis(trifluoromethyl)phosphinous acid (CF3)(2)P-O-H: An ex...
Dibenzo-7-phosphanorbornadiene Ph<sub>3</sub>PC(H)P<b>A</b> (<b>1</b>, <b>A</b> = C<sub>14</sub>H<...
© 2015 The Royal Society of Chemistry. Air-sensitive and air-stable primary phosphines (RPH2) were c...
CASSCF, CASPT2, CCSD(T), and (U)B3LYP electronic structure calculations have been performed in order...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2018.This electronic...
1. Benzylidenephenylsulfonylacetophenone (I) reacts with trimethyl phosphite (80°, C6H6) to give 2,2...
Newer techniques of phosphole synthesis, particularly those which lead to simple phospholes substit...
Fast development in all areas of life and science over the last 50 years demands versatile, energy e...
The reaction of a stable two-coordinate phosphorus compound, 3,3-dimethyl-2-trimethylsiloxy-1-trimet...
International audienceFive different unsupported transition metal phosphides were synthesized and te...
6 pages Full paperThe gas-phase decomposition of diallylvinylphosphine 1 into C5H5P 12 is studied by...
Journal ArticleThe most widely used phosphorous source in chemical beam epitaxy (CBE) is phosphine ...
Contrary to a previous report, the sulfurisation of phosphorus(III) derivatives by 3-amino-1,2,4-dit...
In solution the PCy3/B(C6F5)3 pair is rapidly deactivated by nucleophilic aromatic substitution. In ...
Caution! Decomposition of excess PCl3 (step A) should be carried out carefully in a fume-hood becaus...
Hoge B, Garcia P, Willner H, Oberhammer H. Bis(trifluoromethyl)phosphinous acid (CF3)(2)P-O-H: An ex...
Dibenzo-7-phosphanorbornadiene Ph<sub>3</sub>PC(H)P<b>A</b> (<b>1</b>, <b>A</b> = C<sub>14</sub>H<...
© 2015 The Royal Society of Chemistry. Air-sensitive and air-stable primary phosphines (RPH2) were c...
CASSCF, CASPT2, CCSD(T), and (U)B3LYP electronic structure calculations have been performed in order...
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2018.This electronic...
1. Benzylidenephenylsulfonylacetophenone (I) reacts with trimethyl phosphite (80°, C6H6) to give 2,2...
Newer techniques of phosphole synthesis, particularly those which lead to simple phospholes substit...
Fast development in all areas of life and science over the last 50 years demands versatile, energy e...
The reaction of a stable two-coordinate phosphorus compound, 3,3-dimethyl-2-trimethylsiloxy-1-trimet...
International audienceFive different unsupported transition metal phosphides were synthesized and te...
6 pages Full paperThe gas-phase decomposition of diallylvinylphosphine 1 into C5H5P 12 is studied by...
Journal ArticleThe most widely used phosphorous source in chemical beam epitaxy (CBE) is phosphine ...
Contrary to a previous report, the sulfurisation of phosphorus(III) derivatives by 3-amino-1,2,4-dit...
In solution the PCy3/B(C6F5)3 pair is rapidly deactivated by nucleophilic aromatic substitution. In ...
Caution! Decomposition of excess PCl3 (step A) should be carried out carefully in a fume-hood becaus...