1221682-30-9

Upstream product

• 98-81-7 1-bromovinylbenzene 
• 590-86-3 isovaleraldehyde 
• 4432-63-7 2-phenylacrolein 

Downstream Products

• 1221682-35-4 C₁₃H₁₆O₂ 
• 1420479-98-6 C₁₆H₂₂O₂ 
• 1460349-71-6 2-(5-methyl-2-phenylhex-1-en-3-yl)isoindoline-1,3-dione 
• 1460349-35-2 5-methyl-2-phenylhex-1-en-3-amine 
• 1420480-31-4 C₁₆H₂₄O₃S 
• 1420480-14-3 C₁₅H₂₂O 
• 1420480-49-4 (E)-N-(7-methyl-4-phenyloct-4-en-1-yl)-3-nitrobenzenesulfonamide 
• 1420479-40-8 (Z)-N-(7-methyl-4-phenyloct-4-en-1-yl)-3-nitrobenzenesulfonamide 

Relevant academic research and scientific papers

Non-enzymatic acylative kinetic resolution of primary allylic amines

A non-enzymatic acetyl transfer-based kinetic resolution of primary allylic amines is reported. The process involves the use of (1S,2S)-1 in conjunction with a supported ammonium salt and affords the corresponding enantio-enriched N-acetylated allylic ami

C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization

A catalytic asymmetric bromocyclization of trisubstituted olefinic amides that uses a C2-symmetric mannitol-derived cyclic selenium catalyst and a stoichiometric amount of N-bromophthalimide is reported. The resulting enantioenriched pyrrolidine products, which contain two stereogenic centers, can undergo rearrangement to yield 2,3-disubstituted piperidines with excellent diastereoselectivity and enantiospecificity.

One-pot synthesis of α,β-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols

Described herein is a one-pot synthesis of α,β-epoxy ketones using a palladium-catalyzed epoxidation-oxidation sequence. Functionalized terminal allylic alcohols are treated with m-CPBA under mild reaction conditions to obtain the α,β-epoxy ketones. The m