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Synthesis, Structure, and Rearrangement of 1,3‐Dibora[5]radialenes
Author(s) -
Enders Markus,
Krämer Albrecht,
Pritzkow Hans,
Siebert Walter
Publication year - 1991
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.199100841
Subject(s) - sigmatropic reaction , derivative (finance) , product (mathematics) , chemistry , medicinal chemistry , stereochemistry , crystallography , mathematics , geometry , business , finance
The new 1,3‐bis(dimethylamino) derivative 1 is isoelectronic with decamethyl[5]radialene. The analogous 1,3‐dimethyl compound 2 undergoes slow 1,5‐sigmatropic H shift to give a 1,3‐diborafulvene. This process is faster in the reaction with [Mo(CO) 6 ], whereby the product is the [Mo(CO) 4 ] complex 3.
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