111900-65-3

Upstream product

• 72486-93-2 1-methoxy-2-methyl-3-trimethylsiloxy-1,3-pentadiene 
• 100-52-7 benzaldehyde 

Downstream Products

• 109278-72-0 (2S,3S,4S)-4-acetoxy-3,5-dimethyl-2-phenyl-2,3-dihydro-4H-pyran 
• 106930-09-0 (2S,3R,6R)-3,5-Dimethyl-6-((R)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran 
• 107079-19-6 (2S,3R,6R)-3,5-Dimethyl-6-((S)-1-methyl-allyl)-2-phenyl-3,6-dihydro-2H-pyran 
• 106930-44-3 (3R,3aR,5S,6S,7S,7aS)-3,6,7a-Trimethyl-5-phenyl-7-phenylselanyl-hexahydro-furo[3,2-b]pyran 

Relevant academic research and scientific papers

An N,N′-dioxide/In(OTf)3 catalyst for the asymmetric hetero-Diels-Alder reaction between Danishefsky's dienes and aldehydes: Application in the total synthesis of triketide

(Chemical Equation Presented) In-teresting catalyst: An asymmetric hetero Diels-Alder reaction between Danishefsky's dienes and various aldehydes using an N,N′-dioxide/In(OTf)3 complex affords highly substituted chiral dihydropyranones with up

Asymmetric Hetero Diels-Alder Reaction Catalyzed by Stable and Easily Prepared CAB Catalyst

A stable chiral (acyloxy)borane (CAB) complex is prepared in situ by mixing a tartaric acid derivative and arylboronic acids at room temperature.A solution of the catalyst is effective in catalyzing hetero Diels-Alder reactions to produce dihydropyrone derivatives of high optical purities.

Asymmetric Hetero Diels-Alder Reaction Catalyzed by Stable and Easily Prepared CAB Catalysts

A stable chiral (acyloxy)borane (CAB) complex is prepared in situ by mixing tartaric acid derivative and arylboric acid at room temperature.A solution of the catalyst is effective to catalyze hetero Diels-Alder reaction to produce dihydropyrone derivative