57032-39-0

Upstream product

• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 35781-78-3 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 99869-99-5 2-(6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-propan-2-ol 
• 3208-32-0 2-hexyltetrahydrofuran 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 23313-03-3 (R)-2-[(3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-hydroxyethyl 4-methylbenzenesulfonate 
• 18439-45-7 3-O-Benzyl-6-desoxy-1,2-O-isopropyliden-α-D-gluco-hexofuranose 
• 41670-98-8 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-xylo-hept-6-enofuranos-5-ulose 
• 19493-09-5 Methylenetriphenylphosphorane 

Downstream Products

• 114244-55-2 3-O-benzyl-5-deoxy-1,2-O-isopropylidene-5-C-methyl-β-L-idofuranose 
• 114244-54-1 [(S)-2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-propoxy]-tert-butyl-dimethyl-silane 

Relevant academic research and scientific papers

A FACILE CONVERSION OF TERTIARY ALCOHOLS TO OLEFINS

An efficient method for the dehydration of tertiary alcohols to obtain olefins in high yield, employing methanesulfonyl chloride-triethylamine and catalytic amount of 4-dimethylaminopyridine in dichloromethane, is described.

1,3,5-TRIDEOXY-3,5-DI-C-METHYL-L-TALITOL: A CHIRON FOR THE C-33-C-37 SEGMENT OF AMPHOTERICIN B

1,3,5-Trideoxy-3,5-di-C-methyl-L-talitol is a potential chiron for the C-33-C-37 segment of amphotericin B.This hexitol has been synthesized from 3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose by a route in which a C-methylene derivative at C-5 is hydr

5-Deoxy-3-O-arylmethyl or substituted arylmethyl-1, 2-0-alkylidene-alpha-D-xylofuranose herbicide derivatives

5-Deoxy-3-0-arylmethyl or substituted arylmethyl-1,2-0-alkylidene-a-D-xylofuranose and 5-C-alkyl and alkenyl derivatives thereof. The compounds are useful as herbicides and plant growth regulators.