نتایج جستجو برای: hypervalent iodine

تعداد نتایج: 22019  

2016
Pushpak Mizar Rebecca Niebuhr Matthew Hutchings Umar Farooq Thomas Wirth

An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of different sulfur nucleophiles allows the flexible synthesis of 1,2-aminothiols from alkenes. By employing chiral iodine(III) reagents, a stereoselective version of the thioamination protocol has also been developed.

Journal: :Chemical communications 2014
Makoto Iwata Kyohei Kanoh Takuya Imaoka Kazuo Nagasawa

Cylindradines A and B, members of the polycyclic pyrrole-imidazole alkaloids (PIAs), are the only congeners bearing a 3-carbamoylpyrrole unit among the PIAs. In this communication, we described a total synthesis of (+)-cylindradine A based on intramolecular Friedel-Crafts type cyclization of pyrrole-aldehyde and oxidative cyclization of tricyclic pyrrolopyrrolidine-guanidine with hypervalent io...

Journal: :Molecules 2015
Siguara Bastos Lemos Silva Adriana Della Torre João Ernesto de Carvalho Ana Lúcia Tasca Gois Ruiz Luiz F Silva

A versatile and metal-free approach for the synthesis of carbocycles and of heterocycles bearing seven- and eight-membered rings is described. The strategy is based on ring expansion of 1-vinylcycloalkanols (or the corresponding silyl or methyl ether) mediated by the hypervalent iodine reagent HTIB (PhI(OH)OTs). Reaction conditions can be easily adjusted to give ring expansion products bearing ...

2014
Nadia O Ilchenko Boris O A Tasch Kálmán J Szabó

An air- and moisture-stable fluoroiodane in the presence of AgBF4 is suitable for selective geminal difluorination of styrenes under mild reaction conditions. One of the CF bonds is formed by transfer of electrophilic fluorine from the hypervalent iodine reagent, while the other one arises from the tetrafluoroborate counterion of silver. Deuterium-isotope-labelling experiments and rearrangemen...

Journal: :Journal of Synthetic Organic Chemistry, Japan 2004

Journal: :Synthesis 2022

Abstract Derivatives of fused 1,2,4-triazines containing heterocyclic and metallocene fragments were obtained by one-pot oxidative cyclization hydrazones in the presence hypervalent iodine(III) reagents. For 1,2,4-triazolo[4,3-a]azines, ability to activate HSF1 was investigated. The compounds shown increase degree activation. It that can be used induce Hsp70 expression decrease extent mutant HT...

2013
Yifan Li Jérôme Waser

The direct alkynylation of benzofurans was achieved for the first time using the hypervalent iodine reagent 1-[(triisopropylsilyl)ethynyl]-1,2-benziodoxol-3(1H)-one (TIPS-EBX) based on the cooperative effect between a gold catalyst and a zinc Lewis acid. High selectivity was observed for C2-alkynylation of benzofurans substituted with alkyl, aryl, halogen and ether groups. The reaction was also...

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