نتایج جستجو برای: chemoselectivity

تعداد نتایج: 401  

Journal: :Chemical communications 2014
Shiqing Li Fan Yang Taiyong Lv Jingbo Lan Ge Gao Jingsong You

Imidazolium salts were conveniently prepared by direct aryl quaternization using arylboronic acids. This process features the tolerance of a broad range of functional groups and excellent chemoselectivity, and is especially effective for the synthesis of unsymmetrical imidazolium salts.

Journal: :Dalton transactions 2018
Ramona Turcas Dóra Lakk-Bogáth Gábor Speier József Kaizer

The present study describes the first example of the hydroxylation of benzaldehydes by synthetic nonheme oxoiron(iv) complexes, where the reactivity, chemoselectivity, and mechanism were strongly influenced by the ligand environment of the iron center.

Journal: :Chemical communications 2010
Gaurav Bhargava Beatriz Trillo Marisel Araya Fernando López Luis Castedo José L Mascareñas

We report a Pd-catalyzed intramolecular [3C + 2C + 2C] cycloaddition between alkylidenecyclopropanes, alkynes and alkenes. The method provides synthetically relevant 5-7-5 tricyclic structures, with good chemoselectivity and complete diastereoselectivity.

Journal: :Chemical communications 2014
Chunghyeon Yu Naeem Iqbal Sehyun Park Eun Jin Cho

A visible light-induced process for selective difluoroalkylation of unactivated alkenes has been developed. The choice of base is crucial for governing the chemoselectivity of the process to produce difluoroalkylated alkanes and alkenes.

Journal: :Journal of the American Chemical Society 2013
Tianning Diao Doris Pun Shannon S Stahl

The dehydrogenation of cyclohexanones affords cyclohexenones or phenols via removal of 1 or 2 equiv of H2, respectively. We recently reported several Pd(II) catalyst systems that effect aerobic dehydrogenation of cyclohexanones with different product selectivities. Pd(DMSO)2(TFA)2 is unique in its high chemoselectivity for the conversion of cyclohexanones to cyclohexenones, without promoting su...

Journal: :Chemical communications 2014
Aditi P Chavannavar Allen G Oliver Brandon L Ashfeld

An umpolung approach toward nitrone construction utilizing a phosphine-mediated addition of 1,2-dicarbonyls to nitroso compounds is reported. The reaction exhibits a high degree of chemoselectivity and provides direct access to isoxazolidines, imines, and trisubstituted alkenes.

Journal: :The Journal of organic chemistry 2009
Andrejs Pelss Esa T T Kumpulainen Ari M P Koskinen

Highly chemoselective conjugate reduction of chiral alpha,beta-unsaturated amino ketones has been developed by using triisopropyl phosphite ligated copper hydride complex. The highlights of the method are wide substrate compatibility and exceptional chemoselectivity.

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