z-logo
Premium
Synthesis, Structure, and Thermolysis of N‐Apical 1,2λ 5 ‐Azaphosphetidines with a Pentacoordinate P Center and the First Observation of Their N‐Equatorial Pseudorotamers
Author(s) -
Kawashima Takayuki,
Soda Tomokazu,
Okazaki Renji
Publication year - 1996
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199610961
Subject(s) - thermal decomposition , chemistry , center (category theory) , decomposition , stereochemistry , phosphorus , crystallography , organic chemistry
C‐apical intermediates are implicated for the first time in the synthesis of olefins by the thermolysis of azaphosphetidines 1 . Compound 1 and its pseudorotamer 2 are the first reported azaphosphetidines containing pentacoordinate phosphorus. R = H, CO 2 Me.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom