1443054-73-6

Basic information

• Product Name: (3R,4R)-3-(1-phenylvinyl)-1-tosylpiperidine-4-carbaldehyde
• Synonyms: (3R,4R)-3-(1-phenylvinyl)-1-tosylpiperidine-4-carbaldehyde
• CAS NO: 1443054-73-6
• Molecular Weight: 369.485
• Mol File: 1443054-73-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4R)-3-(1-phenylvinyl)-1-tosylpiperidine-4-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R)-3-(1-phenylvinyl)-1-tosylpiperidine-4-carbaldehyde(1443054-73-6)
• EPA Substance Registry System: (3R,4R)-3-(1-phenylvinyl)-1-tosylpiperidine-4-carbaldehyde(1443054-73-6)

Safety Data

• Hazardous Substances Data: 1443054-73-6(Hazardous Substances Data)

Upstream product

• 1443054-40-7 (E)-4-methyl-N-(4-oxobutyl)-N-(3-phenylbut-2-en-1-yl)benzenesulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 858005-68-2 N-(4,4-diethoxybutyl)-4-methylbenzenesulfonylamide 

Relevant articles and documents

Enantioselective intramolecular aldehyde α-alkylation with simple olefins: Direct access to homo-ene products

A highly selective method for the synthesis of asymmetrically substituted carbocycles and heterocycles from unactivated aldehyde-olefin precursors has been achieved via enantioselective SOMO-catalysis. Addition of a catalytically generated enamine radical cation across a pendent olefin serves to establish a general asymmetric strategy toward the production of a wide range of formyl-substituted rings with alkene transposition. Conceptually, this novel mechanism allows direct access to "homo-ene"-type products.