874211-87-7

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 874211-85-5 (S)-2-((2R,3S,4aR,8aS)-3-{(2R,4aR,6S,7R,8aS)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-4a,6-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy}-octahydro-pyrano[3,2-b]pyran-2-yl)-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 874211-84-4 tert-Butyl-[2-((2R,4aR,6S,7R,8aS)-7-{(2R,3S,4aR,8aS)-2-[1-(4-methoxy-benzyloxymethyl)-vinyl]-octahydro-pyrano[3,2-b]pyran-3-yloxy}-4a,6-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-ethoxy]-diphenyl-silane 
• 874211-86-6 tert-Butyl-[2-((2R,4aR,6S,7R,8aS)-7-{(2R,3S,4aR,8aS)-2-[(S)-2-(4-methoxy-benzyloxy)-1-methyl-ethyl]-octahydro-pyrano[3,2-b]pyran-3-yloxy}-4a,6-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-ethoxy]-diphenyl-silane 
• 874211-83-3 2-((2R,3S,4aR,8aS)-3-{(2R,4aR,6S,7R,8aS)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-4a,6-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy}-octahydro-pyrano[3,2-b]pyran-2-yl)-acrylic acid methyl ester 
• 874211-94-6 (S)-2-((2R,3S,4aR,8aS)-3-{(2R,4aR,6S,7R,8aS)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-4a,6-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy}-octahydro-pyrano[3,2-b]pyran-2-yl)-propan-1-ol 
• 874211-79-7 1-((2S,3S,4aR,8aS)-3-{(2R,4aR,6S,7R,8aS)-6-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-4a,6-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yloxy}-octahydro-pyrano[3,2-b]pyran-2-yl)-ethanone 
• 874211-78-6 tert-Butyl-{2-[(2R,4aR,6S,7R,8aS)-4a,6-dimethyl-2-phenyl-7-((2R,3S,4aR,8aS)-2-vinyl-octahydro-pyrano[3,2-b]pyran-3-yloxy)-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl]-ethoxy}-diphenyl-silane 

Downstream Products

• 874211-88-8 (2R,4aR,6S,7R,8aS)-4a,6-Dimethyl-7-[(2R,3S,4aR,8aS)-2-((S)-1-methyl-allyl)-octahydro-pyrano[3,2-b]pyran-3-yloxy]-2-phenyl-6-vinyl-hexahydro-pyrano[3,2-d][1,3]dioxine 

Relevant academic research and scientific papers

Convergent synthesis of the FGHI ring segment of yessotoxin

A convergent synthesis of the FGHI ring segment of yessotoxin was achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.