نتایج جستجو برای: trisubstituted imidazoles

تعداد نتایج: 4534  

Journal: :Chemical communications 2005
Yasushi Obora Masahiro Kimura Makoto Tokunaga Yasushi Tsuji

A variety of 1,1,2-trisubstituted-1H-indenes are synthesized by the reaction of aliphatic ketones, aryl-substituted alkynes and NbCl3(DME) in 1,2-dichloroethane under reflux conditions.

2009
James N. Iley Maria Sanchis-Amat Xiaohui Zhang Mark R.J. Elsegood Raymond C. F. Jones Mark R. J. Elsegood

A catalytic method involving carbenoid insertion onto dihydroimidazoles is reported for the generation of dihydroimidazolium ylides, and their subsequent diastereoselective cycloaddition to form pyrrolo[1,2-a]imidazoles © 2009 Elsevier Science. All rights reserved ———

Journal: :Chemical communications 2009
Santiago Carballares Donald Craig Christopher J T Hyland Pengfei Lu Tanya Mathie Andrew J P White

The highly regioselective, stereospecific ring-opening of trisubstituted N-tosylaziridines possessing vinyl and hydroxymethyl groups by sulfone- and sulfide-stablised carbanions is reported.

Journal: :Chemical communications 2006
Christopher G Nasveschuk Nathan T Jui Tomislav Rovis

A highly diastereoselective Lewis acid-mediated [1,3] rearrangement of 1,3-dioxepins is the key step along a modular route to 2,3,4-trisubstituted tetrahydrofurans.

Journal: :Chemical communications 2009
Yasutaka Yatsumonji Yuichiro Atake Akira Tsubouchi Takeshi Takeda

Conjugated dienes were produced with complete regio- and stereoselectivity by the titanocene(ii)-promoted alkylation of propargyl carbonates via the formation of 2,3,4-trisubstituted titanacyclobutenes.

Journal: :Chemical communications 2011
Alexander Paptchikhine Kaori Itto Pher G Andersson

A range of 1,2,4-trisubstituted cyclohexadienes obtained from the Birch reaction were hydrogenated asymmetrically to produce synthetically valuable chiral compounds in high enantio- and diastereoselectivity.

Journal: :Organic & biomolecular chemistry 2009
Yasushi Obora Keisuke Takeshita Yasutaka Ishii

NbCl(3)(DME)-catalyzed [2+2+2] intermolecular cycloaddition of alkynes and alkenes was successfully achieved to give 1,4,5-trisubstituted-1,3-cyclohexadiene derivatives in good yields.

Journal: :Chemical communications 2008
Ian Paterson Natalie A Miller

A concise total synthesis of the antiproliferative macrolide (+)-neopeltolide has been completed, utilising a Jacobsen hetero Diels-Alder reaction to install the trisubstituted tetrahydropyran ring.

Journal: :Chemical communications 2006
L Vijaya Raghava Reddy Abhijeet Deb Roy Raja Roy Arun K Shaw

A new and highly efficient methodology for the construction of synthetically important highly O-functionalized enantiopure 2,3,4-trisubstituted tetrahydrofurans with three contiguous stereocenters is reported.

Journal: :Chemical communications 2012
Shaoyu Li Jie Wu

A novel and straightforward synthetic protocol for the efficient construction of 3',5'-dihydro-1H-spiro[benzo[d]oxepine-2,4'-imidazoles] through a copper(I)-catalyzed reaction between 2-(2-ethynylphenyl)oxirane, sulfonyl azide, and 2-isocyanoacetate is described.

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