Weber, Anna K., Schachtner, Josef, Fichtler, Robert, Leermann, Timo M., Neudoerfl, Joerg M. and Jacobi von Wangelin, Axel (2014). Modular synthesis of cyclic cis- and trans-1,2-diamine derivatives. Org. Biomol. Chem., 12 (28). S. 5267 - 5278. CAMBRIDGE: ROYAL SOC CHEMISTRY. ISSN 1477-0539
Full text not available from this repository.Abstract
Structurally diverse carbocycles with two vicinal nitrogen-substituents were prepared in expedient three-component reactions from simple amines, aldehydes, and nitroalkenes. trans, trans-6-Nitrocyclohex-2-enyl amines were obtained in a one-pot domino reaction involving condensation, tautomerisation, conjugate addition, and nitro-Mannich cyclisation. Upon employment of less nucleophilic carboxamides, a concerted Diels-Alder cycloaddition mechanism operated to give the corresponding cis, trans-nitrocyclohexenyl amides. Both types of substituted carbocycles offer ample opportunities for chemical manipulations at the core and periphery. Ring oxidation with MnO2 affords substituted nitroarenes. Reduction with Zn/HCl provides access to various trans-and cis-diaminocyclohexenes, respectively, in a straight-forward manner. With enantiopure secondary amines, a two-step synthesis of chiral nitrocyclohexadienes was developed (82-94% ee).
Item Type: | Journal Article | ||||||||||||||||||||||||||||
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URN: | urn:nbn:de:hbz:38-450102 | ||||||||||||||||||||||||||||
DOI: | 10.1039/c4ob00913d | ||||||||||||||||||||||||||||
Journal or Publication Title: | Org. Biomol. Chem. | ||||||||||||||||||||||||||||
Volume: | 12 | ||||||||||||||||||||||||||||
Number: | 28 | ||||||||||||||||||||||||||||
Page Range: | S. 5267 - 5278 | ||||||||||||||||||||||||||||
Date: | 2014 | ||||||||||||||||||||||||||||
Publisher: | ROYAL SOC CHEMISTRY | ||||||||||||||||||||||||||||
Place of Publication: | CAMBRIDGE | ||||||||||||||||||||||||||||
ISSN: | 1477-0539 | ||||||||||||||||||||||||||||
Language: | English | ||||||||||||||||||||||||||||
Faculty: | Unspecified | ||||||||||||||||||||||||||||
Divisions: | Unspecified | ||||||||||||||||||||||||||||
Subjects: | no entry | ||||||||||||||||||||||||||||
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URI: | http://kups.ub.uni-koeln.de/id/eprint/45010 |
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