1964
DOI: 10.1002/anie.196406961
|View full text |Cite
|
Sign up to set email alerts
|

A Simple Route to Organogallium Compounds

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
1
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 2 publications
0
1
0
Order By: Relevance
“…2,2′‐Dilithiobiphenyl, 2,2′‐dilithiobiphenyl · 2tmeda, phenylgallium dichloride, 6 , 7 ,and 10 were prepared as described in literature.…”
Section: Methodsmentioning
confidence: 99%
“…2,2′‐Dilithiobiphenyl, 2,2′‐dilithiobiphenyl · 2tmeda, phenylgallium dichloride, 6 , 7 ,and 10 were prepared as described in literature.…”
Section: Methodsmentioning
confidence: 99%
“…[2] While this strategy is well established for the synthesis of arylboron species due to facile migration of aryl ligands from silicon to boron, [3] there are only two examples of ligand redistribution involving boron species and alkylsilanes, both of which involve strong Lewis acidic BBr 3 or BI 3 . [4][5][6] In 1977, Nöth et al [4] reported that N(SiMe 3 ) 3 reacts with BBr 3 to afford MeBBr 2 and N(SiMe 2 Br) 3 (Scheme 1a). Following this report, Haubold et al [5] discovered that the reaction of SiMe 4 with BX 3 (X=Br or I) resulted in the formation of Me n BX 3-n (n=1 or 2) and Me 3 SiBr (Scheme 1b).…”
Section: Introductionmentioning
confidence: 99%