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Journal ArticleDOI

Synthesis of Amines from Norbornane Series

TLDR
In this paper, a synthetic procedure was developed for preparation of exo-oriented di- and tetraamines of the norbornane series by 1,3-dipolar cycloaddition to norbornene and norbornadiene of generated in situ diazomethane followed by reduction of arising pyrazolines catalyzed by Raney nickel.
Abstract
Synthetic procedure was developed for preparation of exo-oriented di- and tetraamines of the norbornane series by 1,3-dipolar cycloaddition to norbornene and norbornadiene of generated in situ diazomethane followed by reduction of arising pyrazolines catalyzed by Raney nickel.

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Journal ArticleDOI

Some Peculiarities of Oxidation of 1-Carbamoyl-Substituted Hexahydro-1H-thieno[3,2-c]pyrazole-4,4-dioxides

TL;DR: New bicyclic derivatives of nitrosulfolane annelated with 1-pyrazoline were obtained by oxidation of 3-aryl-1-carbamoyl-6a-methyl-6-nitro-3a,5,6,6a]-tetrahydro-1H-thieno[3,2-c]pyrazole-4,4-dioxides as discussed by the authors.
Journal ArticleDOI

Synthesis of Amines from Norbornane Series.

TL;DR: In this paper, a synthetic procedure was developed for preparation of exo-oriented di- and tetraamines of the norbornane series by 1,3-dipolar cycloaddition to norbornene and norbornadiene of generated in situ diazomethane followed by reduction of arising pyrazolines catalyzed by Raney nickel.
References
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Reactions and Syntheses in the Organic Chemistry Laboratory

TL;DR: C-C BOND FORMATION Nucleophilic Addition to Aldehydes, Ketones, Carboxylic Acid Derivatives (Esters, Anhydrides) and alpha,beta-Unsaturated Carbonyl Compounds Carbonyls Olefination Alkylation of AldeHydes/Ketones, CARBOXylic Acids, and beta-Dicarbonyls Compounds Reactions of Alkenes via Carbenium Ions Transition-Metal-Catalyzed Reactions Pericyclic Reactions Radical Re
Journal ArticleDOI

Novel Access to Polyazamacrocycles: Non‐Template Cyclization of Terephthalaldehyde and Aliphatic Polyamines

TL;DR: In this article, non-template [2+2] condensation of terephthalaldehyde with bis(3-aminopropyl)amine and N,N'-bis(3-, n-bis(1,2)-diaminoethane leads to macrocyclic systems that can be reduced and derivatized further.
Journal ArticleDOI

Cyclopropanation of Unsaturated Compounds with Diazomethane Generated in situ: A New Efficient and Practical Route to Cyclopropane Derivatives

TL;DR: The synthesis of the title compounds is easily achieved by the Pd-catalysed cyclopropanation of unsaturated compounds with diazomethane generated in situ from N-methyl-N-nitrosourea-KOH in CH2Cl2-Et2O as mentioned in this paper.