135708-89-3

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 135708-79-1 (2R,3S,5S,6R)-1-Benzyloxy-2,6-dimethyl-oct-7-ene-3,5-diol 
• 135708-85-9 C₄₉H₈₄O₇Si₃ 
• 135708-86-0 C₄₉H₈₄O₇Si₃ 
• 135708-84-8 (3R,4S,6S,7R)-8-Benzyloxy-4,6-bis-(tert-butyl-dimethyl-silanyloxy)-3,7-dimethyl-octanoic acid (1S,5R,6S)-6-benzyloxy-5-methoxy-cyclohex-2-enyl ester 
• 135708-83-7 (3R,4S,6S,7R)-8-Benzyloxy-4,6-bis-(tert-butyl-dimethyl-silanyloxy)-3,7-dimethyl-octanoic acid 
• 135708-81-5 (3R,4S,6S,7R)-8-Benzyloxy-4,6-bis-(tert-butyl-dimethyl-silanyloxy)-3,7-dimethyl-octan-1-ol 
• 135708-82-6 (3R,4S,6S,7R)-8-Benzyloxy-4,6-bis-(tert-butyl-dimethyl-silanyloxy)-3,7-dimethyl-octanal 
• 135708-80-4 [(2R,3S,5S,6R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2,6-dimethyl-oct-7-enyloxymethyl]-benzene 
• 135708-77-9 (R)-5-Benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-4-methyl-pentanal 
• 135708-75-7 [1-((R)-2-Benzyloxy-1-methyl-ethyl)-but-3-enyloxy]-tert-butyl-dimethyl-silane 
• 89046-67-3 (5R)-6-benzyloxy-5-methyl-4-hydroxyhex-1-ene 

Downstream Products

• 135708-93-9 (E)-(4R,5S,7S,8R)-5,7-Bis-(tert-butyl-dimethyl-silanyloxy)-9-((1S,3R,4R)-4-hydroxy-3-methoxy-cyclohexyl)-2,4,8-trimethyl-non-2-enoic acid methyl ester 
• 135708-92-8 (2S,3S,5S,6R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-7-((1S,3R,4R)-4-hydroxy-3-methoxy-cyclohexyl)-2,6-dimethyl-heptanal 
• 135708-91-7 (1R,2R,4S)-4-[(2R,3S,5S,6R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-7-hydroxy-2,6-dimethyl-heptyl]-2-methoxy-cyclohexanol 
• 135708-90-6 C₄₂H₇₀O₅Si₂ 

Relevant academic research and scientific papers

Synthetic Studies toward Rapamycin: A Solution to a Problem in Chirality Merger through Use of the Ireland Reaction

A program directed toward a total synthesis of rapamycin is described.This paper reports the synthesis of enoate 36, a fragment that would correspond to carbons 28-49 of rapamycin.The two building blocks required to reach 36 were allylic alcohol 5 and aci