2021
DOI: 10.1021/jacs.1c02606
|View full text |Cite
|
Sign up to set email alerts
|

Trifluoromethyl Thianthrenium Triflate: A Readily Available Trifluoromethylating Reagent with Formal CF3+, CF3, and CF3 Reactivity

Abstract: Here we report the synthesis and application of trifluoromethyl thianthrenium triflate (TT-CF 3 + OTf − ) as a novel trifluoromethylating reagent, which is conveniently accessible in a single step from thianthrene and triflic anhydride. We demonstrate the use of TT-CF 3 + OTf − in electrophilic, radical, and nucleophilic trifluoromethylation reactions.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

1
110
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 155 publications
(111 citation statements)
references
References 59 publications
1
110
0
Order By: Relevance
“…We recently developed an electrochemical strategy to engage oxidatively sensitive nucleophiles in net oxidative alkene difunctionalization reactions . Our approach draws inspiration from Yoshida’s pioneering cation pool work and contributes to a rapidly growing body of literature exploiting oxidized thianthrene derivatives as synthetic intermediates. Specifically, we leveraged electrochemistry to cleanly generate dicationic adducts between unactivated alkenes and thianthrene ( TT ), , a safe and inexpensive reagent. This strategy circumvents the need for oxidatively stable coupling partners in net oxidative alkene functionalization reactions; the oxidative alkene activation event is decoupled from nucleophilic substitution.…”
mentioning
confidence: 99%
“…We recently developed an electrochemical strategy to engage oxidatively sensitive nucleophiles in net oxidative alkene difunctionalization reactions . Our approach draws inspiration from Yoshida’s pioneering cation pool work and contributes to a rapidly growing body of literature exploiting oxidized thianthrene derivatives as synthetic intermediates. Specifically, we leveraged electrochemistry to cleanly generate dicationic adducts between unactivated alkenes and thianthrene ( TT ), , a safe and inexpensive reagent. This strategy circumvents the need for oxidatively stable coupling partners in net oxidative alkene functionalization reactions; the oxidative alkene activation event is decoupled from nucleophilic substitution.…”
mentioning
confidence: 99%
“…Based on the above results and related literature, [3,10,17] In summary, we have developed a novel procedure on carbonylative trifluoromethylation of unactivated alkenes. Catalyzed by copper catalyst, carbonylative difunctionaliza-tion of alkenes with Togin-CF 3 and nitrogen (or oxygen) nucleophiles occurred successfully.…”
Section: Methodsmentioning
confidence: 79%
“…[6] Among the limited achievements, Ding and co-workers reported a rhodium-catalyzed asymmetric hydrogenation of a-or b-trifluoromethylated acrylic acids for their preparation in 2013. [7] In 2020, an original transformation on C(sp 3 )-H trifluoromethylation of unactivated alkanes using CF 3 -Cu III complex was established by Hongs group. [8] Very recently, Studers group realized a cascade radical alkene acyltrifluoromethylation with acid fluorides employing Langlois reagent as the CF 3 source (Scheme 2, a).…”
mentioning
confidence: 99%
“…[2] In the past decades, significant progress have been achieved in the incorporation of CF 3 group into organic molecules. [3] In this context, b-trifluoromethylated carboxylic acid derivates constitute an important component of various bio-active drugs. [4] For example, btrifluoromethylated phenylpropionic acid derivatives have been used as agonists of human peroxisome proliferatoractivated receptor alpha (PPAR) (Scheme 1).…”
mentioning
confidence: 99%