14916-79-1Relevant articles and documents
A Short Total Synthesis of (+/-)-Gephyrotoxin-223AB
Broka, Chris A.,Eng, Kan K.
, p. 5043 - 5045 (1986)
(+/-)-Gephyrotoxin-223AB has been synthesized from 2-carbomethoxycyclopentanone in nine steps by a route utilizing the stereoselective homolytic cyclization of an alkenyl-substituted N-chloropiperidine.
Tert-Butyl Nitrite Promoted Oxidative Intermolecular Sulfonamination of Alkynes to Synthesize Substituted Sulfonyl Pyrroles from the Alkynylamines and Sulfinic Acids
Qi, Zhenjie,Jiang, Yong,Wang, Yanyan,Yan, Rulong
supporting information, p. 8636 - 8644 (2018/06/18)
tert-Butyl nitrite promoted oxidative intermolecular sulfonamination of alkynes to synthesize substituted sulfonyl pyrroles from the alkynylamines and sulfinic acids via tandem addition/cyclization was developed. This reaction is performed well by employing tert-butyl nitrite as the oxidant, and various substituted sulfonyl pyrroles are formed in moderate to good yields with no requirement of metal catalysis.
M -Terphenyl Ethers, a new hydroxy protecting group cleavable under reductive single electron transfer reaction conditions
Azzena, Ugo,Mocci, Sarah,Pisano, Luisa
experimental part, p. 1575 - 1580 (2011/06/24)
m-Terphenyl ethers and, to a lesser extent, 2,6-dimethoxyphenyl ethers, were tested as protected hydroxy derivatives under a variety of reaction conditions. These ethers underwent regioselective cleavage of the aromatic C(1)-O bond under reductive SET reaction conditions using alkali metals in tetrahydrofuran at room temperature. This deprotective procedure was efficiently realized in the presence of several other functional groups, including an acetal, a phenyl alkyl ether, an unprotected alcohol, and carbon-carbon double and triple bonds. Furthermore, m-terphenyl ethers proved stable under different reaction conditions, including acidic hydrolysis and formation and/or employment of different organometallic reagents. Georg Thieme Verlag Stuttgart · New York.
