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 Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Barton's O-acyl thiohydroxamates are very useful to generate alkyl radicals from carboxylic acids via O-acyl thiohydroxamates 1,2 and have been used to form carboncarbon bonds by reacting with sulfonyl cyanides 3 and activated olefins. 4 However, Barton esters 1 have some limitations because they are very reactive, thereby yielding a byproduct resulting from attacking the thiocarbonyl group of Barton ester by alkyl radicals. This problem was solved to some extent by using less reactive O-acyl thiohydroxamates 6 in radical acylation approach. 5,6

Decarboxylative Allylation and Vinylation Approach of Thiohydroxamate Esters