86040-00-8

Upstream product

• 76331-10-7 (R)-1-((4S,5R)-5-(1,3-dithian-2-yl)-2,2-dimethyl-1,3-dioxolan-4-yl)propan-2-ol 
• 65-85-0 benzoic acid 
• 86039-98-7 2,3,5-Tri-O-acetyl-4,6-didesoxy-D-xylo-hexose-trimethylendithioacetal 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 76331-09-4 4,6-Didesoxy-D-xylo-hexose-trimethylendithioacetal 
• 4990-82-3 methyl 4,6-dichloro-4,6-dideoxy-α-D-galactopyranoside 
• 20585-18-6 methyl 4,6-dideoxy-α-D-glucopyranoside 

Downstream Products

• 1054626-10-6 Benzoic acid (S)-2-((4S,5R)-5-formyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-methyl-ethyl ester 
• 863444-52-4 Benzoic acid (S)-2-((4S,5S)-5-ethynyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-methyl-ethyl ester 
• 863444-55-7 benzoic acid 2-(2,2-dimethyl-5-prop-1-ynyl-[1,3]dioxolan-4-yl)-1-methyl-ethyl ester 
• 863444-49-9 6-O-benzoyl-1,1-dibromo-5,7-dideoxy-3,4-O-isopropyliden-L-arabino-hept-1-ene 
• 863444-31-9 benzoic acid 2-[5-(2-iodo-propenyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-1-methyl-ethyl ester 
• 863444-93-3 benzoic acid 2-[2,2-dimethyl-5-(2-methyl-but-1-en-3-ynyl)[1,3]dioxolan-4-yl]-1-methyl-ethyl ester 
• 863445-05-0 Benzoic acid (S)-2-[(4S,5S)-2,2-dimethyl-5-((E)-2-methyl-4-trimethylsilanyl-but-1-en-3-ynyl)-[1,3]dioxolan-4-yl]-1-methyl-ethyl ester 
• 86040-02-0 3-O-Benzoyl-2,4,6-tridesoxy-5-O-tetrahydropyranyl-L-threo-hexose-trimethylendithioacetal 

Relevant academic research and scientific papers

A ring-closing metathesis (RCM)-based approach to mycolactonesa A/B

The total synthesis of the mycobacterial toxins mycolactones A/B (1 a/b) has been accomplished based on a strategy built around the construction of the mycolactone core through ring-closing metathesis. By employing the Grubbs second-generation catalyst, t

New approaches towards the synthesis of the side-chain of mycolactones A and B

New approaches towards the synthesis of the C1′-C16′ side-chain of mycolactones A and B from Mycobacterium ulcerans are reported. Chiral building block 4 (Fig. 2) with the correct stereochemistry was obtained starting from naturally occurring monosacchari

Chiral Building Units from Carbohydrates, VIII. - Syntheses of the Four Isomeric 1,3-Dimethyl-2,9-dioxabicyclononanes

Starting from different compounds, the syntheses of the four isomeric bicyclic acetals 17, 32, 36, and 40 - the title compounds - are described.One of these compounds is supposed to direct the attack of the striped ambrosia beetle Trypodendron lineatum Ol