期刊
ORGANIC LETTERS
卷 19, 期 14, 页码 3835-3838出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01710
关键词
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资金
- School of Chemistry, Cardiff University
- EPSRC [EP/M50631X/1]
- German Academic Exchange Service (DAAD)
- Royal Society [RG150466]
- Engineering and Physical Sciences Research Council [1647922] Funding Source: researchfish
The first one-pot deoxftyanamidation,of alcohols has been developed using N-cyano-N-phenyl-p-methylbenzenesulfonamide (NCTS) as both a sulfonyl transfer reagent and a cyanamide source, accessing a diveite range of tertiary,cyanamides in excellent isolated yields. ThiS approach exploits the underdeveloped desulfonylative (N-S bond cleavage) reactivity pathway of NCTS, which is more Commonly employed for electrophilic C- and N-cyanation processes.
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