251914-75-7

Upstream product

• 188605-67-6 (1-prop-2-ynyl)-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 121237-62-5 2-propynyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 100-39-0 benzyl bromide 
• 251914-74-6 2-(prop-2-ynyl)-4,6-di-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 251914-81-5 C₁₇H₂₀O₆ 
• 251914-80-4 Acetic acid (4S,4aR,5S,6R,7aS,7bS)-5-benzyloxy-6-benzyloxymethyl-4,4a,5,6,7a,7b-hexahydro-2H-1,7-dioxa-cyclopenta[cd]inden-4-yl ester 
• 251914-79-1 (4S,4aR,5S,6R,7aS,7bS)-5-Benzyloxy-6-benzyloxymethyl-4,4a,5,6,7a,7b-hexahydro-2H-1,7-dioxa-cyclopenta[cd]inden-4-ol 

Relevant academic research and scientific papers

Iridoids from carbohydrates via Pauson-Khand reaction: Synthesis of advanced highly oxygenated cyclopentane-annulated pyranosides from D-glucal derivatives

The Pauson-Khand reaction on suitable 4-oxa-hept-1-en-6-ynes (1, 17) obtained from 3,4,6-tri-O-acetyl-D-glucal gives the cyclopentane-annulated pyranosides (2, 18) that can be efficiently and stereoseiectivelly transformed into chiral, advanced, highly oxygenated intermediates (10, 16, 24) for the synthesis of iridoid aglycones.