153995-99-4

Upstream product

• 153996-23-7 (1R,2R)-2-(triisopropylsilyloxy)cyclohexanol 
• 1072-86-2 (1R,2R)-trans-1,2-cyclohexanediol 
• 73881-10-4 (E)-1-bromo-2-hexene 
• 593-71-5 Chloroiodomethane 
• 153996-15-7 (1R,2R)-2-[((E)-Hex-2-enyl)oxy]-cyclohexanol 

Relevant academic research and scientific papers

The use of 1,2-trans-cyclohexanediol as an efficient chiral auxiliary for the asymmetric cyclopropanation of allylic ethers

A new and simple chiral auxiliary derived from optically pure 1,2-trans-cyclohexanediol was developed for the asymmetric Simmons-Smith cyclopropanation of substituted allylic alcohols. Excellent yields and diastereoselectivities were obtained with a variety of olefins.