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Carbene transposition involving double dehydrogenation of an sp3 carbon
Home
Publications
Carbene transposition involving double dehydrogenation of an sp3 carbon
Carbene transposition involving double dehydrogenation of an sp3 carbon
Authors:
JI
Joseph N. Coalter Iii
Joseph N. Coalter Iii
JH
John C. Huffman
John C. Huffman
KC
Kenneth G. Caulton
Kenneth G. Caulton
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7 June 2001
journal article
research article
Published by
Royal Society of Chemistry (RSC)
in
Chemical Communications
No. 13
,
p.
1158-1159
DOI:
10.1039/b102422c
Abstract
Two
benzylic hydrogens of 2,6-Me
2
C
6
H
3
O
−
coordinated to RuCl(PCy
3
)
2
(CHPh)
+
are transferred to the benzylidene ligand, liberating toluene to form a new carbene which is covalently linked to the aryloxide ligand.
Keywords
DEHYDROGENATION
INVOLVING DOUBLE
TRANSPOSITION INVOLVING
CARBENE
ME2C6H3O
BENZYLIC
BENZYLIDENE
COVALENTLY
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