1344980-48-8

Upstream product

• 1075709-09-9 1-O-p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-β-D-glucopyranose 
• 98-88-4 benzoyl chloride 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 3150-20-7 4-methoxyphenyl β-D-glucopyranoside 
• 83-87-4 D-glucose pentaacetate 
• 150-76-5 4-methoxy-phenol 
• 2872-65-3 p-methoxyphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 

Downstream Products

• 23567-05-7 1,6-Anhydro-2,3,4-tri-O-benzoyl-β-D-glucopyranose 
• 1344980-54-6 1-O-p-methoxyphenyl 2,3,4-tri-O-benzoyl-β-D-glucopyranose 

Relevant academic research and scientific papers

Tea leaf perfumery precursor glucoside and synthesizing method thereof

The invention relates to a tea leaf perfumery precursor glucoside and a synthesizing method thereof. The synthesizing method comprises the following steps of synthesizing ten glucosides including aromatic alcohol ( alkanol )-beta -D-glucosides and aromatic alcohol (alkanol )-beta -D-primrose indicans. The synthesizing method disclosed by the invention is a glucoside synthesizing method which is good in selectivity, high in production rate and low in cost.

An efficient and recyclable catalyst for the cleavage of tert-butyldiphenylsilyl ethers

An efficient, chemoselective, and environment-friendly method for the deprotection of tert-butyldiphenylsilyl ethers mediated by triflic acid supported on silica gel is reported. A wide range of tert-butyldiphenylsilyl ethers derived from carbohydrate and saponin residues can be smoothly cleaved in the presence of various types of other protecting groups in good to excellent yields in acetonitrile. This heterogeneous reaction does not require aqueous workup, and the supported catalyst can be readily recycled.