115479-79-3

Upstream product

• 103233-18-7 (4R,5S)-4-Methyl-5-((S)-1-methyl-3-trityloxy-propyl)-dihydro-furan-2-one 
• 21461-84-7 (2S)-tetrahydro-5-oxofuran-2-carboxylic acid 
• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 
• 103233-17-6 (S)-5-((S)-1-Methyl-3-trityloxy-propyl)-5H-furan-2-one 
• 99315-75-0 (-)-5-O-(diphenyl-t-butylsilyl)-2,3-O-(thiocarbonyl)-D-ribono-1,4-lactone 
• 115479-85-1 (R)-3-Benzenesulfinyl-5-((S)-1-methyl-3-trityloxy-propyl)-dihydro-furan-2-one 
• 115479-77-1 (4R,5S)-4-Hydroxy-5-methyl-2-phenylsulfanyl-7-trityloxy-heptanoic acid 
• 115479-81-7 (4S,5R)-4-Methyl-5-((S)-1-methyl-3-trityloxy-propyl)-dihydro-furan-2-one 
• 103233-15-4 (2R,3S)-1-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-5-trityloxy-pentan-2-ol 
• 103246-24-8 (S)-5-((S)-1-Methyl-3-trityloxy-propyl)-3-phenylsulfanyl-dihydro-furan-2-one 
• 103233-14-3 (4S,5S)-5-({[tert-butyl(diphenyl)silyl]oxy}methyl)-4-methyldihydrofuran-2(3H)-one 
• 103233-16-5 4,5-anhydro-2,3-dideoxy-3-C-methyl-1-O-triphenylmethyl-D-threo-pentitol 
• 112031-78-4 (3S,4R)-5-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-pentane-1,4-diol 
• 99315-76-1 (5S)-5-(tert-butyldiphenylsiloxymethyl)-2(5H)-furanone 

Downstream Products

• 103233-19-8 (3R,4S,5S)-3,4-dimethyl-1-O-tert-butyldiphenylsilyl-7-O-triphenylmethyl-heptane-1,4,7-triol 
• 103233-20-1 (3S,5R)-3,5-dimethyl-1-O-tert-butyldiphenylsilyl-7-O-triphenylmethyl-heptane-1,7-diol 
• 115479-80-6 Methanesulfonic acid (1S,2S)-1-[(R)-3-(tert-butyl-diphenyl-silanyloxy)-1-methyl-propyl]-2-methyl-4-trityloxy-butyl ester 
• 103233-23-4 (3R,5R)-3,5-di-C-methyl-1-O-tert-butyldiphenylsilyl-7-O-triphenylmethyl-heptane 1,7-diol 
• 115479-80-6 Methanesulfonic acid (1S,2S)-1-[(S)-3-(tert-butyl-diphenyl-silanyloxy)-1-methyl-propyl]-2-methyl-4-trityloxy-butyl ester 
• 103303-19-1 (3S,4S,5S)-1-(tert-Butyl-diphenyl-silanyloxy)-3,5-dimethyl-7-trityloxy-heptan-4-ol 

Relevant academic research and scientific papers

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 Tactically Novel Alternative to Acyclic Stereoselection Based on the Concept of a Replicating Chiron - 1,3- and 1,4-C-Methyl Substitution

A chiral 4-hydroxymethyl butenolide is used as a template for the stereocontrolled conjugate addition of a C-methyl group.A sequential two-carbon extension and reformation of a lactone with the new side-chain leads to a "replicated" butenolide, which is s