Results 381 to 390 of about 424,465 (437)
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Manganese-Catalyzed Direct Nucleophilic C(sp(2))-H Addition to Aldehydes and Nitriles.
Angewandte Chemie, 2015Herein, a manganese-catalyzed nucleophilic addition of inert C(sp(2))-H bonds to aldehydes and nitriles is disclosed by virtue of a dual activation strategy.
Bingwei Zhou, Yuanyuan Hu, Cong-Hui Wang
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Acute aldehyde syndrome and chronic aldehydism
Mutation Research/Reviews in Genetic Toxicology, 1987Abstract Different types of alcohol dehydrogenase and of aldehyde dehydrogenase lead to different blood acetaldehyde levels. With respect to acetaldehyde levels in human blood 3 types can be distinguished: (1) the normal range, (2) the acute aldehyde syndrome, and (3) the chronic aldehydism.
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Ligand-Controlled Divergent C-H Functionalization of Aldehydes with Enynes by Cobalt Catalysts.
Journal of the American Chemical Society, 2015We describe a highly step and atom economical cobalt-catalyzed cyclization of 1,6-enynes with aldehydes to synthesize functionalized pyrrolidines and dihydrofurans with high chemo- and stereoselectivity.
R. Santhoshkumar+2 more
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Organic Letters, 2015
A one-pot synthesis of phenanthridines and quinolines from commercially available or easily prepared aldehydes has been reported. O-(4-Cyanobenzoyl)hydroxylamine was utilized as the nitrogen source to generate O-acyl oximes in situ with aldehydes ...
Xiao-De An, Shouyun Yu
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A one-pot synthesis of phenanthridines and quinolines from commercially available or easily prepared aldehydes has been reported. O-(4-Cyanobenzoyl)hydroxylamine was utilized as the nitrogen source to generate O-acyl oximes in situ with aldehydes ...
Xiao-De An, Shouyun Yu
semanticscholar +1 more source
Access to nitriles from aldehydes mediated by an oxoammonium salt.
Angewandte Chemie, 2015A scalable, high yielding, rapid route to access an array of nitriles from aldehydes mediated by an oxoammonium salt (4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate) and hexamethyldisilazane (HMDS) as an ammonia surrogate has
C. Kelly+5 more
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Accounts of Chemical Research, 2015
Chemists no longer doubt the importance of a methodology that could activate and utilize aldehydes in organic syntheses since many products prepared from them support our daily life.
Y. Hoshimoto, M. Ohashi, S. Ogoshi
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Chemists no longer doubt the importance of a methodology that could activate and utilize aldehydes in organic syntheses since many products prepared from them support our daily life.
Y. Hoshimoto, M. Ohashi, S. Ogoshi
semanticscholar +1 more source
Journal of Organic Chemistry, 2015
The combination of a catalytic amount of InCl3 and acetic anhydride remarkably promotes the Knoevenagel condensation of a variety of aldehydes and activated methylene compounds.
Yohei Ogiwara+3 more
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The combination of a catalytic amount of InCl3 and acetic anhydride remarkably promotes the Knoevenagel condensation of a variety of aldehydes and activated methylene compounds.
Yohei Ogiwara+3 more
semanticscholar +1 more source
Journal of Organic Chemistry, 1996
Sodium triacetoxyborohydride is presented as a general reducing agent for the reductive amination of aldehydes and ketones. Procedures for using this mild and selective reagent have been developed for a wide variety of substrates.
A. Abdel-Magid+4 more
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Sodium triacetoxyborohydride is presented as a general reducing agent for the reductive amination of aldehydes and ketones. Procedures for using this mild and selective reagent have been developed for a wide variety of substrates.
A. Abdel-Magid+4 more
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Synthesis from Aldehydes by Substitution of the Aldehyde Hydrogen
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
X. Franck, B. Figadere
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Stereodivergent α-allylation of linear aldehydes with dual iridium and amine catalysis.
Journal of the American Chemical Society, 2014We describe the fully stereodivergent, dual catalytic α-allylation of linear aldehydes. The reaction proceeds via direct iridium-catalyzed substitution of racemic allylic alcohols with enamines generated in situ.
S. Krautwald+3 more
semanticscholar +1 more source