TY  - JOUR
N2  - A library of pinane-based aminodiols were prepared from commercially available (1R)-(-)-myrtenol (-)-1. Compound (-)-1 was transformed into ally! trichloroacetamide (+)-2 via the acetimidate, followed by the Overman rearrangement. In order obtain the aminodiol structure, (+)-2 was subjected to stereoselective dihydroxylation with OsO4, resulting in dihydroxy trichloroacetamide (+)-3. The trichloroacetyl group was removed from (+)-3 with aqueous HCl and the (1R,2R,3S,5R)-3-amino-2-hydroxymethyl-6,6-dimethylbicyclo[3.1.1]heptan-2-ol hydrochloride (-)-4 obtained was transformed to primary, secondary and tertiary aminodiols by reductive amination, N-alkylation of aminodiol (+)-9 and debenzylation of N-benzyl aminodiol (+)-10, respectively. In the reactions of (+)-9 and (+)-14 with formaldehyde, highly regioselective ring closure was observed. In contrast with earlier results, the aminodiols gave pinane-fused oxazolidines (+)-11 and (-)-15. The aminodiols and their oxazolidine derivatives 5-15 were applied as chiral catalysts in the enantioselective addition of diethylzinc to benzaldehyde. The best enantioselectivity was observed in the case of the N-benzyl-substituted derivative (+)-9. (C) 2012 Elsevier Ltd. All rights reserved.
UR  - http://publicatio.bibl.u-szeged.hu/10398/
SP  - 144
JF  - TETRAHEDRON-ASYMMETRY
TI  - Stereoselective synthesis of pinane-type tridentate aminodiols and their application in the enantioselective addition of diethylzinc to benzaldehyde
IS  - 2
N1  - FELTÖLT?: Németh József Lukács - nemethl@pharm.u-szeged.hu
WC: Chemistry, Inorganic & Nuclear; Chemistry, Organic; Chemistry, Physical
SN  - 0957-4166
VL  - 23
EP  - 150
AV  - restricted
ID  - publicatio10398
A1  -  Csillag Kinga Karola
A1  -  Németh Lukács
A1  -  Martinek Tamás
A1  -  Szakonyi Zsolt
A1  -  Fülöp Ferenc
Y1  - 2012///
ER  -