1994
DOI: 10.1016/0022-1139(93)05008-o
|View full text |Cite
|
Sign up to set email alerts
|

Reaction of hexafluorobenzene with trimethylsilyl ethers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
10
0

Year Published

1999
1999
2016
2016

Publication Types

Select...
5
1
1

Relationship

0
7

Authors

Journals

citations
Cited by 15 publications
(10 citation statements)
references
References 15 publications
0
10
0
Order By: Relevance
“…Several attempts to synthesize C 6 (OFc) 6 failed, because of the low thermal stability of 1 compared with C 6 H 5 OH . Compound 6e is the second example of a molecule bearing five ether and one fluoro substituent …”
Section: Resultsmentioning
confidence: 99%
“…Several attempts to synthesize C 6 (OFc) 6 failed, because of the low thermal stability of 1 compared with C 6 H 5 OH . Compound 6e is the second example of a molecule bearing five ether and one fluoro substituent …”
Section: Resultsmentioning
confidence: 99%
“…Similar nucleophilic substitution of alkoxide anion equivalent 9 on an aromatic ring was achieved by the reaction of silyl ethers with hexafluorobenzene 7 in the presence of a catalytic amount of CsF as an initiator (Scheme 4) [4]. It was reported that the use of silyl ethers was more favorable for polyalkoxylation of 7 than alkali metal alkoxide.…”
Section: Intermolecular Desilylative-defluorination Reactionmentioning
confidence: 85%
“…When Me 3 SiCl/Et 3 N, was used, only a poor yield of the silylated product SCHEME 1 2a was formed, but in the case of hexamethyldisilazane with a catalytic amount of sodium saccharin [3], the silyl ethers 2a and 2b were formed in high yield irrespective of the fluoroalkyl chain length (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
“…The filtrate was dried in vacuo, giving 6a as very hygroscopic solid. 9,9,9,8,8,7,7,6,6,5,5,4,4- 3 P, 40%], 1.0 (s, 7A) and 1.7 (s, 7B, 60%). After 1 day: d ‫ס‬ 1.0 and 1.7 (60%), 114.0 (40%).…”
Section: General Procedures For Silylation Of Hydroxy Ketones 1abmentioning
confidence: 99%