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Modeling of sedimentation and filtration layer formation by discrete element method

ДОМИНО-РЕАКЦИИ 1-АРОИЛ-3,4-ДИГИДРОИЗОХИНОЛИНОВ С СИММЕТРИЧНЫМИ АЛКИНАМИ

Synthesis and Properties of 3-Substituted 2H-Chromen-2-ones-amino-3-sulfanylidenepropanoate, 3-amino-N-aryl-3-sulfanylidenepropanamides, and ethyl 2-(1,3-thiazol-2

Synthesis of Functionalized Partially Hydrogenated Quinolines by a Stork Reaction - Intramolecular Transamination - Alkylation Tandem Protocol-amino-4-(2,5-dimethoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide were

Synthesis of Functionalized Partially Hydrogenated Quinolines by a Stork Reaction — Intramolecular Transamination — Alkylation Tandem Protocol-amino-4-(2,5-dimethoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide were

Multicomponent synthesis and molecular structure of 3-amino-2-aroyl(alkoxycarbonyl, arylcarbamoyl)-4-aryl(hetaryl)-5-arylcarbamoyl-6-methylthieno[2,3-b]pyridines groups. The structures of 3-amino-2-benzoyl-4-(furan-2-yl)-6-methyl-N-phenylthieno[2,3-b]pyridine-5

Novel routes towards synthesis of pyrrolo[2,1-a]isoquinolines

New approach to the synthesis of pyrrolo[2,1-a]isoquinolines by the reaction of 1-aroyl-3,4-dihydroisoquinolines with symmetric alkynes

Domino reactions of 1-aroyl-3,4-dihydroisoquinolines with ?,?-unsaturated aldehydes

Domino reactions of 4-aroyl-6,7-dihydrothienopyridines with electron deficient alkynes and alkenes

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