727429-07-4

Upstream product

• 100-39-0 benzyl bromide 
• 954406-23-6 (R)-2-(1-Allyloxy-2-ethoxy-allyl)-1,4-dioxa-spiro[4.5]decane 
• 727428-80-0 1-(R)-1,4-Dioxa-spiro[4.5]dec-2-yl-2-ethoxy-prop-2-en-1-ol 
• 727428-88-8 (2R)-2-[(1S,2S,5R)-1-ethoxy-3-oxabicyclo[3.2.0]hept-2-yl]-1,4-dioxa-spiro[4.5]decane 
• 954406-25-8 (1S,2R,5R)-2-benzyl-1-ethoxy-3-oxabicyclo[3.2.0]heptane-2-carboxylic acid methyl ester 
• 727428-94-6 (1S,2R,5R)-1-ethoxy-3-oxabicyclo[3.2.0]heptane-2-carboxylic acid methyl ester 
• 78008-36-3 (R)-2,3-cyclohexylideneglyceraldehyde 
• 954406-28-1 ((1S,2R,5R)-2-Benzyl-1-ethoxy-3-oxa-bicyclo[3.2.0]hept-2-yl)-methanol 

Relevant academic research and scientific papers

Asymmetric induction in copper (I)-catalyzed intramolecular [2 + 2] photocycloaddition: Synthesis of enantiopure cyclobutane derivatives

A simple approach for asymmetric induction in copper (I)-catalyzed intramolecular [2 + 2] photocycloaddition of 1,6-dienes, where asymmetric catalysis or chiral auxiliaries have been inefficient, has been developed using the concept of chirality transfer

Copper(I)-catalyzed intramolecular asymmetric [2 + 2] photocycloaddition. Synthesis of both enantiomers of cyclobutane derivatives

Equation presented. A simple approach for asymmetric induction in Cu(I)-catalyzed [2 + 2] photocycloaddition, where asymmetric catalysts or chiral auxiliaries were inefficient, has been developed using the concept of chirality transfer from the readily av