(±)-1α-Nitro-2β-[3-(6-chloropyridyl)]-cyclohexanone, a key intermediate for a stereocontrolled synthesis of the alkaloid epibatidine, possessing a 7-azanorbornane structure to which is attached, in an exo-orientation, a 5-(2-chloropyridyl) substituent, has been prepared either by Diels-Alder reaction or tandem Michael reaction by way of 5-(2-nitrovinyl)-2-chloropyridine as common starting material and 2-trimethylsilyloxy-1,3-butadiene or methyl 3-oxo-4-pentenoate as counterparts respectively.

Total synthesis of (+/-)-epibatidine

BARCO, Achille;BENETTI, Simonetta;DE RISI, Carmela;POLLINI, Gian Piero;ROMAGNOLI, Romeo;ZANIRATO, Vinicio
1994

Abstract

(±)-1α-Nitro-2β-[3-(6-chloropyridyl)]-cyclohexanone, a key intermediate for a stereocontrolled synthesis of the alkaloid epibatidine, possessing a 7-azanorbornane structure to which is attached, in an exo-orientation, a 5-(2-chloropyridyl) substituent, has been prepared either by Diels-Alder reaction or tandem Michael reaction by way of 5-(2-nitrovinyl)-2-chloropyridine as common starting material and 2-trimethylsilyloxy-1,3-butadiene or methyl 3-oxo-4-pentenoate as counterparts respectively.
1994
Albertini, E.; Barco, Achille; Benetti, Simonetta; DE RISI, Carmela; Pollini, Gian Piero; Romagnoli, Romeo; Zanirato, Vinicio
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/461251
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