13296-94-1Relevant articles and documents
An engineered linker capable of promoting on-resin reactions for microwave-assisted solid-phase organic synthesis
Sun, Li-Ping,Dai, Wei-Min
, p. 7255 - 7258 (2006)
An active link: A diglycine-containing linker (cat·linker) was fabricated on Rink amide resin for dual functions: a) attachment of a scaffold and b) capture of metal ions for promoting on-resin reactions (see picture). The metal-catching feature of the li
Stereospecific 1,3-Aminobromination of Donor–Acceptor Cyclopropanes
Das, Saikat,Daniliuc, Constantin G.,Studer, Armido
, p. 11554 - 11558 (2017)
Sn(OTf)2-catalyzed 1,3-aminobromination of donor–acceptor cyclopropanes with various sulfonyl amides or electron-poor anilines and N-bromosuccinimide is reported. These experimentally straightforward reactions occurred with complete regio- and
Rhodium-Catalyzed Synthesis and Optical Properties of Silicon-Bridged Arylpyridines
Shintani, Ryo,Misawa, Nana,Takano, Ryo,Nozaki, Kyoko
, p. 2660 - 2665 (2017)
A convergent and regioselective synthesis of silicon-bridged 4-arylpyridines has been developed through a rhodium-catalyzed [2+2+2] cycloaddition of silicon-containing diynes with nitriles. The absorption and emission properties of these compounds have be
DEOXYNOJIRIMYCIN DERIVATIVES AS GLUCOSIDASE INHIBITORS
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Paragraph 0716, (2022/01/22)
The present invention relates to novel iminosugars and their use as glucosidase inhibitors. The present inventors discovered that certain deoxynojirimycin derivatives may be effective in inhibiting glucosidases. In particular, such deoxynojirimycin derivatives may be useful for treating a disease or condition in which inhibition of glucosidase may play an important role.
A Practical Procedure for Regioselective Bromination of Anilines
Takahashi, Yusuke,Seki, Masahiko
, p. 1828 - 1832 (2021/04/15)
A highly practical procedure for the preparation of bromoanilines by using copper-catalyzed oxidative bromination has been developed. Treatment of free anilines with readily available NaBr and Na 2S 2O 8in the presence of a catalytic amount of CuSO 4·5H 2O enabled regioselective bromination.
Cu-mediated selective bromination of aniline derivatives and preliminary mechanism study
Zhao, Hong-Yi,Yang, Xue-Yan,Lei, Hao,Xin, Minhang,Zhang, San-Qi
supporting information, p. 1406 - 1415 (2019/05/01)
A simple and efficient bromination of aniline, aniline derivatives, and analogs have been developed. Forty three examples were given and the highest yield reached was 98%. Different substrates including substituted aniline, pyridin-amine, N-substituted aniline, N,N-disubstituted aniline, N-phenyl-amide, N-phenyl-sulfonamide, and nitrogen-containing heterocycles were all reactive and selectively generated desired bromo-products. The method can be applied to synthesize drug intermediate and quinoxaline derivatives.