English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Plus monthly

Global: Zendy Tools annual

Global: Zendy Tools monthly

Global: Zendy Free Plan

The recent progresses of the application of trifluoromethanesulfonyl chloride, CF 3 SO 2 Cl, in the formation of C-CF 3 , C-SCF 3 , C-SOCF 3 , and C-Cl bonds are summarised in this second part of a two-part review published back-to-back on both sodium trifluoromethanesulfinate, CF 3 SO 2 Na, (Part 1) and trifluoromethanesulfonyl chloride, CF 3 SO 2 Cl (Part 2). There are many reactions in common between these two reagents but it should be noted that CF 3 SO 2 Cl reacts under reductive conditions while CF 3 SO 2 Na requires oxidative conditions. Electrophilic chlorination is obviously the exclusive preserve of CF 3 SO 2 Cl that has been exploited with emphasis in enantioselective chlorination.

beilstein journal of organic chemistry

CF3SO2X (X = Na, Cl) as reagents for trifluoromethylation, trifluoromethylsulfenyl-, -sulfinyl- and -sulfonylation and chlorination. Part 2: Use of CF3SO2Cl