RESUMEN
A total synthesis of the proposed structures of fulicineroside and its aglycone fulicinerine is reported. The tetrasubstituted dibenzofuran substructure was accessible either through a Pd-mediated ortho-metalation or by an Ir-catalyzed meta-borylation. The synthesis of the ß,ß,α-linked trisaccharide consisting of D-olivose, L-rhodinose, and L-rhamnose was challenged by the unprecedented ß-linked rhodinose. A Pd-catalyzed ß-selective glycosylation of a 4-epi-rhodinose and a subsequent Mitsunobu inversion provided selectively the ß-linked L-rhodinose-L-rhamnose disaccharide. Comparison with the reported data for the natural product and the aglycone suggests a misassignment of the structure of the natural product.
Asunto(s)
Benzofuranos/química , Benzofuranos/síntesis química , Productos Biológicos/síntesis química , Desoxiazúcares/química , Disacáridos/síntesis química , Glicósidos/síntesis química , Productos Biológicos/química , Disacáridos/química , Glicósidos/química , Glicosilación , Trisacáridos/síntesis químicaRESUMEN
Ring closing metathesis of d-glucose derived diene-substrate containing nitrogen functionality followed by asymmetric dihydroxylation afforded sugar substituted dihydroxylated pyrrolidines 8a-c which on 1,2-acetonide deprotection and reductive amination afforded putative uniflorine A 2a and its analogues 2b-c, respectively.
Asunto(s)
Alcaloides/síntesis química , Indolizinas/síntesis química , Alcaloides/química , Hidroxilación , Indolizinas/química , Espectroscopía de Resonancia Magnética , Estructura Molecular , EstereoisomerismoRESUMEN
The Johnson-Claisen rearrangement of D-gluco and L-ido-derived allylic orthoesters afforded gamma,delta-unsaturated ester that on ester reduction, epoxidation, regioselective oxirane opening by sodium azide and hydrogenation led to sugar amino alcohols--immediate precursors for 1-deoxy-homonojirimycin 3a,b, and polyhydroxylated homoazepanes 4a,b. Our synthetic approach and glycosidase inhibitory activity is reported.
Asunto(s)
1-Desoxinojirimicina/análogos & derivados , 1-Desoxinojirimicina/farmacología , Azepinas/farmacología , Glicósido Hidrolasas/antagonistas & inhibidores , 1-Desoxinojirimicina/síntesis química , 1-Desoxinojirimicina/química , Animales , Azepinas/síntesis química , Azepinas/química , Bovinos , Hidroxilación/efectos de los fármacos , Concentración 50 Inhibidora , Conformación Molecular , Plantas/enzimología , Levaduras/enzimologíaRESUMEN
Conjugate addition of n-butyl amine to d-glucose derived alpha,beta-unsaturated ester 4 afforded beta-amino esters 5a,b that on reduction of ester group, 1,2-acetonide deprotection, and reductive amination led to the formation of corresponding N-butyl 1-deoxy-D-gluco-homonojirimycin 2c and N-butyl 1-deoxy-L-ido-homonojirimycin 2d which were found to be selective beta-glucosidase inhibitors with an IC(50) value in millimolar range.
Asunto(s)
1-Desoxinojirimicina/análogos & derivados , Inhibidores Enzimáticos/síntesis química , Glicósido Hidrolasas/antagonistas & inhibidores , Piperidinas/síntesis química , 1-Desoxinojirimicina/síntesis química , 1-Desoxinojirimicina/farmacología , Aminación , Inhibidores Enzimáticos/farmacología , Iminopiranosas/síntesis química , Iminopiranosas/farmacología , Concentración 50 Inhibidora , Modelos Químicos , Piperidinas/farmacologíaRESUMEN
The intramolecular aminomercuration reaction of sugar-derived beta-hydroxy-gamma-alkenylamines 8a-c undergoes 5-endo-trig cyclization in high yield. The sugar-substituted pyrrolidines thus obtained were elaborated to the synthesis of polyhydroxylated indolizidine alkaloids, namely, castanospermine 1a, 1-epi-castanospermine 1b, and 8a-epi-castanospermine 1c, having promising glycosidase inhibitory activities.
Asunto(s)
Indolizinas/síntesis química , Pirrolidinas/síntesis química , Aminas/química , Ciclización , Glucosidasas/antagonistas & inhibidores , Mercurio/químicaRESUMEN
The Johnson-Claisen rearrangement of D-glucose-derived allylic alcohols 5a,b, afforded sugar-substituted gamma,delta-unsaturated ester in high yield. Conversion of the ester group to an azidomethyl group, epoxidation of the double bond and hydrogenation gave pyrrolidine ring skeletons 13a and 13b, which were transformed to tetrahydroxy perhydroaza-azulenes 1a and 1b, respectively. Glycosidase inhibitory activity was also evaluated.
RESUMEN
[reaction: see text] The synthesis and evaluation of glycosidase inhibitory activity of polyhydroxylated indolizidine alkaloids namely 2-hydroxy-1-deoxycastanospermine 3a,b and 2-hydroxy-1-deoxy-8a-epi-castanospermine 3c,d is reported. The key step involves the intermolecular 1,3-dipolar cycloaddition of allyl alcohol to d-glucose-derived nitrone 4, followed by tosylation, that afforded four diastereomeric sugar-substituted isoxazolidines 5a-d with the desired regioselectivity. The one-pot conversion of 5a-d to pyrrolidines 8a-d by hydrogenolysis, removal of 1,2-acetonoide functionality, and hydrogenation afforded corresponding target molecules 3a-d.
Asunto(s)
Glucosa/química , Óxidos de Nitrógeno/química , Propanoles/química , Glicósido Hidrolasas/antagonistas & inhibidores , Glicósido Hidrolasas/metabolismo , Indolizinas , Concentración 50 Inhibidora , Conformación Molecular , Estructura Molecular , EstereoisomerismoRESUMEN
The asymmetric dihydroxylation of a d-glucose derived alpha,beta-unsaturated ester 3 afforded syn vicinal diols in good to high diastereoselectivity. The conversion of these vicinal diols to the corresponding cyclic sulfate, regio-, stereoselective nucleophilic ring opening by sodium azide, and LAH reduction afforded amino heptitols 7a,b that were converted to azepane 1c,d and nojirimycin analogues 2c,d.