879283-02-0

Upstream product

• 850588-50-0 (2R,4R)-2-[2-(tert-butyldiphenylsilyloxy)ethyl]-4-(triisopropylsilyloxy)-3,4-dihydro-2H-pyran 
• 389123-32-4 C₂₈H₄₄O₂Si₂ 
• 347189-30-4 (±)-1-((tert-butyldiphenylsilyl)oxy)hex-5-en-3-ol 
• 850588-48-6 (3R,5R)-7-(tert-butyldiphenylsilyloxy)-5-(triethylsilyloxy)-3-(triisopropylsilyloxy)hept-1-yne 
• 850588-45-3 (3R,5R)-7-(tert-butyldiphenylsilyloxy)-5-(triethylsilyloxy)-1-(trimethylsilyl)hept-1-yn-3-ol 
• 850588-49-7 (3R,5R)-1-(tert-butyldiphenylsilyloxy)-5-(triisopropylsilyloxy)hept-6-yn-3-ol 
• 850588-47-5 (3R,5R)-7-(tert-butyldiphenylsilyloxy)-5-(triethylsilyloxy)hept-1-yn-3-ol 

Relevant academic research and scientific papers

Stereocontrolled synthesis of spiroketals via Ti(Oi-Pr)4- mediated kinetic spirocyclization of glycal epoxides with retention of configuration

A Ti(Oi-Pr)4-mediated kinetic spiroketalization reaction has been developed for the stereocontrolled target- and diversity-oriented synthesis of spiroketals. In contrast to most existing methods for spiroketal synthesis, this reaction does not

Enantioselective synthesis of erythro-4-deoxyglycals as scaffolds for target- And diversity-oriented synthesis: New insights into glycal reactivity

An efficient, enantioselective synthesis of eryithro-4-deoxygtycals has been developed using asymmetric aldehyde allylation and tungsten-catalyzed alkynol endo-cycloisomerization as the key steps. These versatile synthetic scaffolds have been elaborated t