405915-30-2

Upstream product

• 405914-77-4 tert-Butyl-diphenyl-[4-((1R,5S,7R)-7-vinyl-6,8-dioxa-bicyclo[3.2.1]oct-2-en-5-yl)-butoxy]-silane 
• 405914-82-1 [4-((4R,5R)-2-Allyl-4,5-divinyl-[1,3]dioxolan-2-yl)-butoxy]-tert-butyl-diphenyl-silane 
• 405915-07-3 tert-Butyl-{4-[(4R,5R)-2-(3-chloro-propyl)-4,5-divinyl-[1,3]dioxolan-2-yl]-butoxy}-diphenyl-silane 
• 111-29-5 1 ,5-pentanediol 
• 131216-47-2 5-(tert-butyldiphenylsilyloxy)pentanal 
• 121671-76-9 5-(tert-butyldiphenylsilyloxy)pentan-1-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 405915-62-0 tert-butyl-{4-[2-(3-chloro-propyl)-[1,3]dithian-2-yl]-butoxy}-diphenyl-silane 
• 405915-02-8 8-(tert-butyl-diphenyl-silanyloxy)-1-chloro-octan-4-one 
• 405914-97-8 2-(4'-(tert-butyldiphenylsilyloxy)butane)-1,3-dithiane 

Downstream Products

• 405915-35-7 (1R,2S,3S,5S,7R)-3-Bromo-5-[4-(tert-butyl-diphenyl-silanyloxy)-butyl]-7-vinyl-6,8-dioxa-bicyclo[3.2.1]octan-2-ol 

Relevant academic research and scientific papers

Dioxolane-to-bridged acetal-to-spiroketal via ring-closing metathesis and rearrangement: A novel route to 1,7-dioxaspiro[5.5]undecanes

(Equation Presented) Several examples of 1,7-dioxaspiro[5.5]undecane spiroketal systems have been synthesized from the common bicyclic intermediate 1 via acid-catalyzed rearrangement. Intermolecular ketalization of C2 symmetric diene diol 3 wit