855855-53-7

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 444809-61-4 (3R)-5-[(4-methoxyphenyl)methoxy]pent-1-yn-3-ol 
• 444809-59-0 (2S,3R)-2-Chloromethyl-3-[2-(4-methoxy-benzyloxy)-ethyl]-oxirane 
• 2746-25-0 p-Methoxybenzyl bromide 
• 146916-76-9 5-(4-methoxyphenyl)methoxy-2-pentyn-1-ol 
• 158817-21-1 (E)-5-(4-methoxybenzyloxy)pent-2-en-1-ol 
• 218434-90-3 1-but-3-ynyloxymethyl-4-methoxy-benzene 
• 242808-65-7 ((2R,3R)-3-(2-(4-methoxybenzyloxy)ethyl)oxiran-2-yl)methanol 

Downstream Products

• 855855-51-5 Benzoic acid (1S,3S,7R)-7-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-9-(4-methoxy-benzyloxy)-1-phenethyl-non-5-ynyl ester 
• 954134-26-0 C₂₇H₄₄O₇Si 
• 954134-47-5 C₃₁H₄₈O₉Si 
• 954134-51-1 C₃₁H₅₀O₉Si 
• 1158818-59-7 C₃₀H₄₈O₆Si 
• 1158818-67-7 C₃₀H₄₈O₆Si 
• 1158818-58-6 C₂₂H₃₄O₅Si 
• 855855-59-3 (E)-(3S,5S,9R)-9-(tert-Butyl-dimethyl-silanyloxy)-11-(4-methoxy-benzyloxy)-1-phenyl-undec-7-ene-3,5-diol 
• 855855-61-7 tert-Butyl-{(E)-(R)-4-((4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-1-[2-(4-methoxy-benzyloxy)-ethyl]-but-2-enyloxy}-dimethyl-silane 
• 855855-63-9 (2Z,6E)-(R)-5-(tert-Butyl-dimethyl-silanyloxy)-8-((4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-octa-2,6-dienoic acid ethyl ester 
• 855855-62-8 (E)-(R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-((4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-hex-4-en-1-ol 

Relevant academic research and scientific papers

A convergent approach for the total synthesis of (-)-synrotolide diacetate

A simple carbohydrate based convergent approach towards the total synthesis of (-)-synrotolide diacetate is described employing a Sharpless asymmetric epoxidation, a Grignard assisted lactol opening with a terminal alkyne and a Wittig reaction using the H

A carbohydrate-based approach for the total synthesis of strictifolione

A chiral pool approach starting with D-glucose, using the Yamaguchi protocol and a Z-selective HWE reaction followed by lactonization, has been applied to execute the total synthesis of strictifolione.