231609-90-8

Upstream product

• 231609-87-3 (S)-2-Benzyloxyamino-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-isopropyl-pent-4-en-1-one 
• 231609-88-4 C₂₇H₃₅NO₅ 
• 66222-05-7 (E)-1-bromo-4-methyl-2-pentene 
• 124-63-0 methanesulfonyl chloride 

Relevant academic research and scientific papers

Asymmetric synthesis of L-azetidine-2-carboxylic acid and 3-substituted congeners - Conformationally constrained analogs of phenylalanine, naphthylalanine, and leucine

Enantiopure L-azetidine-2-carboxylic acid, the (3R)-phenyl, (3R)- naphthyl and (3S)-isopropyl analogs were prepared based on a zinc-mediated asymmetric addition of allylic halides to the camphor sultam derivative of glyoxylic acid O-benzyl oxime.