Total, asymmetric synthesis of methyl 3-deoxy-3-(1 ',2 ',6 '-trideoxy-2 ',6 '-imino-D-galactitol-1-yl)-alpha-D-manno-pyranoside (A C-linked imino disaccharide): Conformational analysis and glycosidase inhibition

Citation
C. Marquis et al., Total, asymmetric synthesis of methyl 3-deoxy-3-(1 ',2 ',6 '-trideoxy-2 ',6 '-imino-D-galactitol-1-yl)-alpha-D-manno-pyranoside (A C-linked imino disaccharide): Conformational analysis and glycosidase inhibition, SYNTHESIS-S, 1999, pp. 1441-1452
Citations number
75
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
SYNTHESIS-STUTTGART
ISSN journal
00397881 → ACNP
Year of publication
1999
Pages
1441 - 1452
Database
ISI
SICI code
0039-7881(1999):<1441:TASOM3>2.0.ZU;2-1
Abstract
The lithium enolate 16 derived in 5 steps from the Diels-Alder adduct of fu ran to 1-cyanovinyl (1S)-camphanate [(+)-12: a "naked sugar" of the first g eneration] was reacted with (+)(1R,4S,5S,6S)-6-endo-chroro-3-methylidene-5- exo-phenylseleno-7-oxabicyclo[2.2.1]. heptan-2-one [(+)-8] to give a unique product of Michael addition after acidic quenching. This adduct (-)-18 was transformed into branched long-chain carbohydrate derivatives such as benz yl 5-deoxy-5-[(5"-O-acetyl-3"-deoxy-2"-O-methoxymethyl-D-manno-furanurono-6 , 1-lactone-3''-yl)methyl]- (tert-butyl)dimethylsilyl-2,3-di-O-methoxymethy l-alpha and beta-L-gulo-furanosideuronate [(-)-27]. Hydrogenolysis, followe d by a Curtius rearrangement permitted to construct the corresponding branc hed 5-amino-5,6-dideoxydodecose derivative (-)-30 which was converted into 5-O-acetyl-3- [ 5'-N-(benzyloxy)carbonyl-2',3'-di-O-methoxymethyl-alpha and beta-D-manno-furanose]-2-O-methoxymethyl-D-manno-furanurono-6, 1-lactone [ (-)-31] and then into methyl 3-deoxy-3-(1',2',6'-trideoxy-2',6'-imino-D-gal actitol-1'-yl)-alpha-D-manno-pyranoside [(-)-1]. Its H-1 NMR spectrum measu red at variable temperature demonstrated that (-)-1 exist as a double equil ibrium involving two pairs of rotamers about the sigma C(1')-C(2') and sigm a C(1')-C(3) bond [CH2 bridge linking beta-C(I) of the I,5-dideoxy-1,5-imin o-D-lyxitol unit at C(3) of methyl alpha-D-manno-pyranoside]. Rotamers B' i n which C(3) is gauche with respect to C(3') is preferred to conformers C' in which C(3) is anti with respect to C(3'). An equilibrium constant K (B' = C') congruent to 0.35 (25 degrees C) was evaluated. Rotamers B [C(2) gauc he with respect to C(2')] and C [C(2) anti with respect to C(2')] are equal ly populated. Disaccharide mimetic (-)-1 is a moderate inhibitor of alpha-L -fucosidases from bovine liver (K-i = 100 mu M) and human placenta.