1615707-75-9

Upstream product

• 1615707-42-0 (3R,4S,5S)-4-methyl-1-phenyl-5,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)hexan-3-yl acetate 
• 83173-74-4 (3S,4R)-3-methyl-6-phenyl-1-hexen-4-ol 
• 1615707-40-8 C₂₅H₄₂B₂O₅ 
• 1615707-73-7 (3R,4S)-4-methyl-1-phenylhex-5-en-3-yl acetate 
• 1615707-74-8 C₁₅H₂₂O₄ 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 1615707-76-0 tert-butyldiphenyl(((4R,5R,6R)-2,2,5-trimethyl-6-phenethyl-1,3-dioxan-4-yl)methoxy)silane 

Relevant academic research and scientific papers

Hydroxyl-directed stereoselective diboration of alkenes

An alkoxide-catalyzed directed diboration of alkenyl alcohols is described. This reaction occurs in a stereoselective fashion and is demonstrated with cyclic and acyclic homoallylic and bishomoallylic alcohol substrates. After oxidation, the reaction generates 1,2-diols such that the process represents a method for the stereoselective directed dihydroxylation of alkenes.