The 2-phosphaethynolate anion: a convenient synthesis and [2+2] cycloaddition chemistry.

Symplectic ID
416556
Source
PubMed
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Sunday, 10 May, 2026 - 00:06
DOI
10.1002/anie.201305235
Publication Date
Monday, 16 September, 2013
First Page
10064
Last Page
10067
Keywords
cycloaddition
organophosphorus chemistry
phosphaethynolate anion
phosphorus
polyphosphides
Authors
Jupp, AR
Goicoechea, JM
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Abstract
Hip to be square: Direct carbonylation of solutions of the heptaphosphide trianion (P7(3-)) afforded the phosphaethynolate anion in moderate yields. This species undergoes [2+2] cycloaddition reactions with diphenylketene and bis(2,6-diisopropylphenyl)carbodiimide to yield the anionic four-membered heterocycles P[C(O)]2C(C6H5)2(-) and PC(O)(CNDipp)NDipp(-) .
Journal Title
Angew Chem Int Ed Engl
eISSN
1521-3773
Volume
52
Issue
38
ID at Source
23913436
Publication Status
Published
Open access
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