PHOSPHORYLATION OF PHENOLS AND NAPHTHOLS BY PHENYLMETHYLENEPHOSPHINE OXIDE GENERATED BY THE THERMOLYSIS OF A 2-PHOSPHABICYCLO[2.2.2]OCTA-5,7-DIENE 2-OXIDE-Reference-Cited by-同舟云学术

PHOSPHORYLATION OF PHENOLS AND NAPHTHOLS BY PHENYLMETHYLENEPHOSPHINE OXIDE GENERATED BY THE THERMOLYSIS OF A 2-PHOSPHABICYCLO[2.2.2]OCTA-5,7-DIENE 2-OXIDE

Published:2001-01 Issue:11 Volume:31 Page:1737-1741
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Keglevich Gy.,Szelke H.,Dobó A.,Nagy Z.,Toke L.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1081/SCC-100104403

Reference11 articles.

1. Photochemical fragmentation of the 2-phosphabicyclo[2.2.2]octa-5,7-diene ring system as a versatile method for generating 3-coordinate methylene phosphine oxides and sulfides

2. GENERATION OF P-DIALKYLAMINO METHYLENEPHOSPHINE OXIDES BY THE PHOTOCHEMICAL FRAGMENTATION OF 2-DIALKYLAMINO-2-PHOSPHABICYCLO[2.2.2]-OCTA-5,7-DIENE 2-OXIDES

3. Photolysis of the cycloadduct of a 1,2-dihydrophosphinine oxide with N -phenylmaleimide in the presence of protic species: new aspects on the mechanism of the fragmentation of a 2-phosphabicyclo[2.2.2]octene

4. Phosphorylation of Amines by the UV-light Mediated Fragmentation of a 2-Phosphabicyclo[2.2.2]octene 2-Oxide

5. Evidence for the involvement of pentacoordinate P-intermediates during the UV light-mediated fragmentation of a 2-phosphabicyclo[2.2.2]octene 2-oxide in the presence of O-nucleophiles

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