Revised structure of a homonojirimycin isomer from Aglaonema treubii: first example of a naturally occurring alpha-homoallonojirimycin.
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P. Compain | H. Kizu | O. Martin | O R Martin | P Compain | H Kizu | N Asano | N. Asano
[1] J. Romeo,et al. α-Homonojirimycin and 2,5-dihydroxymethyl-3,4-dihydroxy-pyrrolidine: Alkaloidal glycosidase inhibitors in the moth Urania fulgens , 1990 .
[2] B. Winchester,et al. Iminoheptitols as glycosidase inhibitors: Synthesis of α-homomannojirimycin, 6-epi-α-homomannojirimycin and of a highly substituted pipecolic acid , 1992 .
[3] Y. Auberson,et al. Total Synthesis of Allonojirimycin (5-Amino-5-Deoxy-D-Allopyranose) , 1989 .
[4] P. D. Lilley,et al. Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases. , 1998, Journal of medicinal chemistry.
[5] Paul S. Liu. Total synthesis of 2,6-dideoxy-2,6-imino-7-O-(.beta.-D-glucopyranosyl)-D-glycero-L-gulo-heptitol hydrochloride. A potent inhibitor of .alpha.-glucosidases , 1987 .
[6] Chi‐Huey Wong,et al. Enzyme-catalyzed organic synthesis: practical routes to aza sugars and their analogs for use as glycoprocessing inhibitors , 1993 .
[7] G. Kite,et al. α-Homonojirimycin [2,6-dideoxy-2,6-imino-d-glycero-l-gulo-heptitol] from omphalea diandra L.: isolation and glucosidase inhibtion , 1988 .
[8] G. Fleet,et al. Amino-sugar glycosidase inhibitors: versatile tools for glycobiologists. , 1992, Glycobiology.
[9] Satoshi Ishii,et al. Accelerated transport and maturation of lysosomal α–galactosidase A in Fabry lymphoblasts by an enzyme inhibitor , 1999, Nature Medicine.
[10] K. Matsui,et al. Homonojirimycin Isomers and Glycosides from Aglaonema treubii , 1997 .
[11] Li Liu,et al. Synthesis of “α-Homogalactostatin” and of its 1,N-anhydro derivative , 1995 .