نتایج جستجو برای: trisubstituted imidazole

تعداد نتایج: 7707  

Journal: :Chemical & pharmaceutical bulletin 2000
A Wada Y Nomoto K Tano E Yamashita M Ito

Palladium catalyzed cross coupling reactions of a vinyl triflate intermediate and various alkenyl stannanes afforded trisubstituted Z-olefins stereoselectively in high yields. These olefins were then converted to the corresponding 9Z-retinoic acids via Horner-Emmons reaction and subsequent basic hydrolysis in excellent yields.

Journal: :Chemical communications 2018
P V Santhini A S Smrithy C P Irfana Jesin Sunil Varughese Jubi John K V Radhakrishnan

A Pd-catalyzed synthesis of 3,4,5-trisubstituted cyclopentenes from diazabicyclic olefins and o-iodobenzoates has been developed. The hitherto unknown cascade process involves three stages: carbopalladation, oxypalladation and a Tsuji-Trost reaction. We have also developed a facile route involving a novel benzylic C-H activation towards cyclopentenoindane moieties.

Journal: :Chemical communications 2011
Ozora Kubo Kenzo Yahata Tomohiro Maegawa Hiromichi Fujioka

A diastereoselective ring contraction of the diastereomixture of 2,4-disubstituted 1,3-dioxepins to 2,5-cis-2,3,5-trisubstituted tetrahydrofurans was achieved using TfOH in DMF. The reaction appears to proceed via a chair-like transition state, in which stereomutation of the oxocarbenium occurred, followed by an aldol-type cyclization.

2014
David M. Barber Andrej Ďuriš Amber L. Thompson Hitesh J. Sanganee Darren J. Dixon

The highly enantioselective preparation of trisubstituted pyrrolidine derivatives employing a one-pot nitro-Mannich/hydroamination cascade is reported. This cascade approach utilizes an asymmetric bifunctional organocatalytic nitro-Mannich reaction followed by a gold-catalyzed allene hydroamination reaction. The products are afforded in good yields and excellent diastereo- and enantioselectivit...

Journal: :Angewandte Chemie 2015
J Stephen Clark Filippo Romiti Kirsten F Hogg Malai Haniti S A Hamid Sven C Richter Alistair Boyer Joanna C Redman Louis J Farrugia

Chloroacetic acid promotes an efficient and diastereoselective intramolecular cascade reaction of electron-deficient ynenones to deliver products featuring a 2,3,5-trisubstituted furan bearing a fused cyclopropyl substituent at the 5-position. Synthetically relevant polycyclic building blocks featuring rings of various sizes and heteroatoms have been synthesized in high yield using this mild ac...

Journal: :Chemical & pharmaceutical bulletin 2016
Keisuke Tomohara Koji Kasamatsu Tomoyuki Yoshimura Takumi Furuta Takeo Kawabata

Enantioselective intramolecular conjugate addition reactions of short-lived C-O axially chiral enolates have been developed. The reactions proceeded with inversion of the configuration and provided dihydrobenzofurans with contiguous tetra- and trisubstituted carbon centers in up to 96% enantiomeric excess (ee).

Journal: :Organic & biomolecular chemistry 2008
Nandkishkor Chandan Mark G Moloney

2,2,5-Trisubstituted pyrrolidines are available from allylic pyroglutamates by Ireland-Claisen ester rearrangement followed by Eschenmoser sulfide contraction and reduction in a highly diastereoselective and efficient sequence. Some of the products from this sequence exhibit activity against S. aureus, but are much less active against E. coli.

Journal: :Clinical chemistry 1970
R Humbel

DURING A STUDY on the metabolism of histidine in a child affected with histidinemia (Beauvais, P., and Humbel, R., to be published), we became interested in the chromatography of imidazoles. In this disease the urine contains numerous imidazoles: histidine and its metabolites, imidazole-pyruvic, imidazole-lactic and imidazole-acetic acids and N-acetylhistidine.’I developed a chromatographic met...

Journal: :Biochemistry 1999
S J Admiraal B Schneider P Meyer J Janin M Véron D Deville-Bonne D Herschlag

The nonenzymatic reaction of ATP with a nucleophile to generate ADP and a phosphorylated product proceeds via a dissociative transition state with little bond formation to the nucleophile. Consideration of the dissociative nature of the nonenzymatic transition state leads to the following question: To what extent can the nucleophile be activated in enzymatic phosphoryl transfer? We have address...

Journal: :Justus Liebig's Annalen der Chemie 1893

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