110013-33-7

Upstream product

• 111971-12-1 (Z)-(R)-8,9-Bis-benzyloxy-non-6-enal oxime 
• 111971-10-9 (Z)-(R)-8,9-Bis-benzyloxy-non-6-en-1-ol 
• 111971-14-3 (E)-(R)-8,9-Bis-benzyloxy-non-6-enal oxime 
• 109960-73-8 (E)-(S)-8,9-Bis-benzyloxy-non-6-enal oxime 
• 68760-65-6 (6-hydroxyhexyl)triphenylphosphonium bromide 
• 20196-70-7 (+)-(R)-2,3-bis(benzyloxy)propanal 

Relevant academic research and scientific papers

Stereoselective Intramolecular Nitrile Oxide Cycloaddition to Chiral Allyl Ethers

Intramolecular nitrile oxide cycloaddition reactions on (Z)- and (E)-chiral allyl ethers occur with poor to good stereoselectivity (diastereoisomeric ratios up to 86:14), which depends on the double bond configuration as well as on steric and stereoelectr

Stereoselectivity of Intramolecular Nitrile Oxide Cycloadditions to Z and E Chiral Alkenes

Intramolecular nitrile oxide cycloaddition (INOC) reactions on chiral alkenes were studied in order to evaluate the influence of the double bond configuration on the stereochemical outcome of the process.Oximes 11-16 were prepared, starting from aldehydes