نتایج جستجو برای: 4 dihydroquinoline 3 carbohydrazide

تعداد نتایج: 2481523  

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

Journal: :Marine Drugs 2008
Yutthapong Sangnoi Oraphan Sakulkeo Supreeya Yuenyongsawad Akkharawit Kanjana-opas Kornkanok Ingkaninan Anuchit Plubrukarn Khanit Suwanborirux

Acetylcholinesterase-inhibiting activity of marinoquinoline A (1), a new pyrroloquinoline from a novel species of a marine gliding bacterium Rapidithrix thailandica, was assessed (IC(50) 4.9 microM). Two related pyrrole derivatives, 3-(2'-aminophenyl)-pyrrole (3) and 2,2-dimethyl-pyrrolo-1,2-dihydroquinoline (4), were also isolated from two other strains of R. thailandica. The isolation of 3 fr...

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

Journal: :Oriental journal of chemistry 2022

Benzofurans display a wide array of pharmaceutical activities. The present work incorporates the synthesis some novel benzofuran derivatives. compound 1 (z)-3-amino-7methoxy-N1-(2-oxoindolin-3-yliedene)benzofuran-2-carbohydrazide was synthesized by refluxing carbohydrazide and isatin. formed key intermediate for compounds 2a-c. structures prepared derivatives were established physical spectral ...

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

Journal: :Organic & biomolecular chemistry 2007
Yuji Mikata Shiho Aida Yoko Inaba Shigenobu Yano

The regio- and enantioselectivity of the reduction of an NAD model compound having axial chirality with respect to the C(3)(quinolinium)-C(carbonyl) bond, 3-piperidinylcarbonyl-1,2,4-trimethylquinolinium ion (1), by using several reducing agents is described. Reaction of 1 with sodium hydrosulfite affords the 1,4-reduced product, 3-piperidinylcarbonyl-1,2,4-trimethyl-1,4-dihydroquinoline (), wi...

Journal: :Organic & biomolecular chemistry 2014
Xue-Qiang Chu You Zi Hua Meng Xiao-Ping Xu Shun-Jun Ji

A transition-metal-free process for the synthesis of 1,4-dihydroquinoline derivatives starting from simple enaminones with aldehydes via intermolecular cascade cyclization in a one-pot protocol is developed. This methodology affords a variety of products in moderate to good yields. Particularly, the use of the enaminone fragment in 1,4-dihydroquinoline derivatives 3 as a leaving group for furth...

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