106820-44-4

Upstream product

• 5418-86-0 tris(methylthio)methane 
• 99315-76-1 (5S)-5-(tert-butyldiphenylsiloxymethyl)-2(5H)-furanone 
• 39090-54-5 tris(methylthio)methyl lithium 
• 21461-84-7 (2S)-tetrahydro-5-oxofuran-2-carboxylic acid 
• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 
• 5336-08-3 D-Ribono-1,4-lactone 
• 99315-75-0 (-)-5-O-(diphenyl-t-butylsilyl)-2,3-O-(thiocarbonyl)-D-ribono-1,4-lactone 
• 92512-33-9 (3R,4S,5R)-5-((tert-butyldiphenylsilyloxy)methyl)-3,4-dihydroxydihydrofuran-2(3H)-one 
• 106731-86-6 (S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-phenylselanyl-dihydro-furan-2-one 
• 102717-29-3 (5S)-5-({[tert-butyl(diphenyl)silyl]oxy}methyl)dihydrofuran-2(3H)-one 
• 56-86-0 L-glutamic acid 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 106820-45-5 (3S,4S,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-4-(tris-methylsulfanyl-methyl)-dihydro-furan-2-one 
• 105676-50-4 (R)-5-[(R)-1-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-ethyl]-3-phenylsulfanyl-dihydro-furan-2-one 
• 115479-84-0 (R)-3-Benzenesulfinyl-5-[(R)-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl]-dihydro-furan-2-one 
• 115495-43-7 (4R,5R)-5-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-hydroxy-2-phenylsulfanyl-hexanoic acid 
• 105676-31-1 1,2-anhydro-3,4,5,6-tetradeoxy-3,5-di-C-methyl-5-O-tert-butyldiphenyl-silyl-D-arabino-heptitol 
• 115495-40-4 (2S,3S,4S)-5-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-pentane-1,2,4-triol 
• 105676-29-7 3,4,5,6-tetradeoxy-3,5-di-C-methyl-7-O-tert-butyldiphenylsilyl-D-arabino-heptitol 
• 105676-34-4 (3R,4S,5R,7S)-1,4,9-trihydroxy-3,5,7-trimethyl-9-O-tert-butyldiphenylsilyl-nonane 
• 115495-41-5 1-O-tert-butyldiphenylsilyl-3-deoxy-4,5-O-isopropylidene-3-C-methyl-D-arabinitol 
• 105676-32-2 (S)-5-[(1R,3S)-5-(tert-Butyl-diphenyl-silanyloxy)-1,3-dimethyl-pentyl]-5H-furan-2-one 
• 105676-56-0 3,4,5,6-tetradeoxy-1,2-O-isopropylidene-3,5-di-C-methyl-7-O-tert-butyldiphenylsilyl-D-arabino-heptitol 
• 105676-33-3 (4R,5S)-5-[(1R,3S)-5-(tert-Butyl-diphenyl-silanyloxy)-1,3-dimethyl-pentyl]-4-methyl-dihydro-furan-2-one 
• 105676-54-8 3,5,6-dideoxy-1,2-O-isopropylidene-3,5-di-C-methyl-7-O-tert-butyldiphenylsilyl-D-altro-heptitol 
• 115495-42-6 3-deoxy-3-C-methyl-1-O-(2,4,6-triisopropyl)benzenesulfonyl-D-arabinitol 

Relevant academic research and scientific papers

Research on L-Nucleosides. Synthesis and biological evaluation of a series of L- and D-2′,3′-Dideoxy-3′-[tris(methylthio)methyl]-β- pentofuranosyl nucleosides

Novel nucleoside analogues of both D and L enantiomeric series were prepared by coupling reaction between a 2′,3′-dideoxy-3′-modified furanose moiety and four different nucleobases. Though in all cases anomeric mixtures of nucleosides were obtained, the p

STEREOCHEMICAL CONTROL OF NATURE'S BIOSYNTHETIC PATHWAYS: A GENERAL STRATEGY FOR THE SYNTHESIS OF POLYPROPIONATE-DERIVED STRUCTURAL UNITS FROM A SINGLE CHIRAL PROGENITOR

A general strategy that permits the stereocontrolled construction of acyclic chains containing vicinal and/or alternating alkyl and hydroxy substituents is presented.Structural subunits of ionomycin were synthesized from a common chiral intermediate.

A Versatile Protocol for the Stereocontrolled Elaboration of Vicinal Secondary and Tertiary Centers of Relevance to Natural Product Synthesis

Chiral butenolides derived from L-glutamic acid, D-ribonolactone, or D-mannitol are versatile templates from the stereocontrolled introduction of functional groups.Vicinal and/or alternating patterns of secondary and tertiary substitution can be attained