REAL

Ring closure reactions of bicyclic prolinol and prolin ester enantiomers

Palkó, Márta and Molnar, Zs. and Kivela, H. and Sinnkonen, J. and Pihlaja, K. and Fülöp, Ferenc (2009) Ring closure reactions of bicyclic prolinol and prolin ester enantiomers. ARKIVOC, & (Part 6). pp. 221-234. ISSN 1551-7004

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Abstract

Starting from the of bicyclic proline ester, ethyl exo-2-azabicyclo[2.2.1]heptane-3-carboxylate (+)-5 several hydantoines and thiohydantoines were prepared by acidic ring closure of the corresponding urea or thiourea derivatives. Enantiomer (-)-5 was reduced to 2-azanorbornylmethanol 12, which was transformed to 5,8-methanooxazolo- and thiazolo[3,4-a] pyridine derivatives. The structures, stereochemistry and relative configurations of the synthesized compounds were proved by NMR.

Item Type: Article
Uncontrolled Keywords: Bicyclic prolinol, enantioselective synthesis, epimerisation, ring closure, 1,3-heterocycles
Subjects: Q Science / természettudomány > QD Chemistry / kémia
R Medicine / orvostudomány > RM Therapeutics. Pharmacology / terápia, gyógyszertan
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 22 May 2014 20:27
Last Modified: 22 May 2014 20:27
URI: http://real.mtak.hu/id/eprint/12863

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