92512-38-4

Upstream product

• 92512-37-3 (3S,5S)-3-acetoxy-5-<(diphenyl-t-butylsilyloxy)methyl>dihydrofuran-2(3H)-one 
• 102717-30-6 (3R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-3-hydroxy-dihydro-furan-2-one 
• 5336-08-3 D-Ribono-1,4-lactone 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 92512-33-9 (3R,4S,5R)-5-((tert-butyldiphenylsilyloxy)methyl)-3,4-dihydroxydihydrofuran-2(3H)-one 
• 92512-35-1 2,3-di-O-acetyl-5-O-diphenyl-t-butylsilyl-D-ribonic acid γ-lactone 
• 92512-36-2 (5S)-3-acetoxy-5-<(diphenyl-t-butylsilyloxy)-methyl>furan-2(5H)-one 
• 102717-29-3 (5S)-5-({[tert-butyl(diphenyl)silyl]oxy}methyl)dihydrofuran-2(3H)-one 

Downstream Products

• 102717-39-5 (S)-1-(tert-Butyl-diphenyl-silanyloxy)-3-((R)-2,2-diethyl-[1,3]dioxolan-4-yl)-propan-2-ol 
• 106747-80-2 (S)-5-((R)-2,2-Diethyl-[1,3]dioxolan-4-ylmethyl)-5H-furan-2-one 
• 106731-90-2 (S)-5-((R)-2,2-Diethyl-[1,3]dioxolan-4-ylmethyl)-3-phenylselanyl-dihydro-furan-2-one 
• 92512-39-5 (2S,4S)-5-diphenyl-t-butylsilyloxy-2,4-dihydroxypentyl 2,4,6-tri-isopropylbenzenesulphonate 
• 92512-42-0 (3S,5S)-3,5-bis(dimethyl-t-butylsilyloxy)-6-(diphenyl-t-butylsilyloxy)hexanenitrile 
• 92512-40-8 (3S,5S)-6-Diphenyl-t-butylsilyloxy-3,5-dihydroxyhexanenitrile 
• 92512-41-9 (2S,4S)-5-(diphenyl-t-butylsilyloxy)-4-hydroxy-1,2-epoxypentane 
• 1391927-45-9 C₃₇H₄₈O₅Si 
• 1391927-43-7 C₃₆H₄₆O₅Si 
• 1391927-42-6 C₃₆H₄₈O₅Si 
• 1391927-41-5 C₄₀H₅₄O₆Si 
• 1391927-38-0 C₄₂H₅₈O₈Si 
• 1391927-64-2 C₅₆H₈₀O₉Si₂ 
• 1391927-37-9 C₄₂H₅₈O₈Si 

Relevant academic research and scientific papers

METHODOLOGY FOR THE POLYENE AND RELATAD ANTIBIOTICS-ENANTIOSPECIFIC SYNTHESIS OF CHIRAL STRUCTURAL UNITS OF AMPHOTERICIN B FROM A COMMON PROGENITOR:THE C14-C20 AND C32-C38 SEGMENTS

Structural units corresponding to the C14-C20 and C32-C3 segments of amphotericin B were synthesized from a single chiral progenitor.

A Tactically Novel Alternative to Acyclic Stereoselection Based on the Concept of a Replicating Chiron - Access to 1,3-Polyols

(S)-Glutamic acid is used as a chiral template to construct seven carbon subunits containing alternating hydroxyl groups with stereochemical control.Enantiomeric and/or diastereomeric 3,5-dideoxy-heptitols are thus obtained.

A Convenient Procedure for the Deoxygenation and Homologation of D-Ribose Derivatives

5-O-Acetyl- and 5-O-diphenyl-t-butylsilyl-2,3-di-O-acetyl-D-ribonolactones were converted into the corresponding 3-deoxy-2-O-acetyl-D-arabinolactone derivatives (9a) and (9b) by sequential reaction with 1,8-diazabicycloundec-7-ene and hydrogen over