نتایج جستجو برای: regio and chemoselective

تعداد نتایج: 16827812  

Journal: :journal of sciences, islamic republic of iran 2015
m. j. taghizadeh f. salahi m. hamzelooian k. jadidi

an efficient, one-pot, four-component procedure for the synthesis of a small library of new chiral spiro- oxindolopyrrolidines with high regio-, diastereo- (>99:1 dr), and enantioselectivity (up to 80% ee) is described. in this process, the regio- and stereochemical 1,3-dipolar cycloaddition of azomethine ylides, which were generated insitu by the reaction of isatin derivatives and sarcosin,wit...

Journal: :Chemical communications 2011
Saikat Khamarui Deblina Sarkar Palash Pandit Dilip K Maiti

A general strategy for fast decarboxylative difunctionalization to gem-dihalohydrin, gem-dihaloether, gem-dibromoester and cyclized bromo-1,4-dioxane synthons with outstanding regio- and stereoselectivity is demonstrated.

Journal: :Chemical communications 2011
Masahito Murai Ryo Hatano Sachie Kitabata Kouichi Ohe

Treatment of arylacetylenes and cyanogen bromide in ClCH(2)CH(2)Cl with a catalytic amount of GaCl(3) afforded (Z)-β-bromoacrylonitriles with high regio- and stereoselectivity.

Journal: :Chemical communications 2014
Kenta Tatsumi Tetsuaki Fujihara Jun Terao Yasushi Tsuji

Palladium-catalyzed formal arylacylation of allenes using acid chlorides and arylboronic acids has been achieved. The reaction afforded the corresponding α,β-unsaturated ketones regio- and stereoselectively.

Journal: :Organic & biomolecular chemistry 2012
Andrew K Swenson Kate E Higgins Matthew G Brewer William W Brennessel Michael G Coleman

A convenient Cu(I)-catalyzed cycloaddition of electron rich internal aryl alkynes and diazoacetates was discovered for the chemoselective and regioselective synthesis of tetra-substituted furans and cyclopropenes in moderate isolated yields (18-67%), and alkyne conversion (29-73%).

Journal: :Chemical communications 2012
Nozomi Saito Yuh Kohyama Yuki Tanaka Yoshihiro Sato

Ruthenium-catalyzed cyclization of 1,6-allenynes occurs via the addition of heteroatom nucleophiles to ruthenacyclopentenes, providing functionalized 1,2-bisalkylidenecyclopentanes in a highly regio- and stereoselective manner.

Journal: :Chemical communications 2007
Akihiro Ooguri Zenichi Ikeda Seijiro Matsubara

Treatment of thiol ester with bis(iodozincio)alkane in the presence of palladium catalyst followed by silylation affords Z-silyl enol ether chemo-, regio- and stereoselectively.

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