Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
about
Recent developments in and perspectives on three-coordinate boron materials: a bright future.Cleavage of Unstrained C-C Bonds in Acenes by Boron and Light: Transformation of Naphthalene to Benzoborepin.Synthesis of a Doubly Boron-Doped Perylene through NHC-Borenium Hydroboration/C-H Borylation/Dehydrogenation.An Isolable Diboron-Centered Diradical with a Triplet Ground State.How Boron Doping Shapes the Optoelectronic Properties of Canonical and Phenylene-Containing Oligoacenes: A Combined Experimental and Theoretical Investigation.Addition of dihydrogen to a borylborenium center.A redox-active diborane platform performs C(sp3)-H activation and nucleophilic substitution reactions.
P2860
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P2860
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@en
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@nl
type
label
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@en
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@nl
prefLabel
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@en
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@nl
P2093
P2860
P356
P1476
Reversible Dihydrogen Activation by Reduced Aryl Boranes as Main-Group Ambiphiles.
@en
P2093
Esther von Grotthuss
Hans-Wolfram Lerner
Martin Diefenbach
Matthias Wagner
Max C Holthausen
Michael Bolte
P2860
P304
14067-14071
P356
10.1002/ANIE.201608324
P407
P577
2016-10-06T00:00:00Z