144899-41-2

Upstream product

• 63-91-2 L-phenylalanine 
• 67-64-1 acetone 
• 3182-95-4 L-Phenylalaninol 

Downstream Products

• 155185-83-4 1-((S)-4-Benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-chloro-ethanone 
• 205437-40-7 (2E,4S)-2,2-dimethyl-3-(2-methyl-1-oxo-2-butenyl)-4-phenylmethyloxazolidine 
• 171736-89-3 (S)-4-benzyl-2,2-dimethyl-3-propanoyloxazolidine 
• 144899-50-3 (S)-3-acryloyl-4-benzyl-2,2-dimethyloxazolidine 
• 155185-91-4 2-(Benzhydrylidene-amino)-1-((S)-4-benzyl-2,2-dimethyl-oxazolidin-3-yl)-ethanone 
• 216219-26-0 1-((S)-4-Benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-phenylselanyl-butane-1,3-dione 

Relevant academic research and scientific papers

Chiral auxiliary mediated stereoselective allylation of electron deficient radicals

Electron deficient radicals bearing oxazolidine chiral auxiliaries undergo efficient addition to allyltributyltin with moderate to excellent stereoselectivities.

Synthesis of chiral γ-lactams via Rh(II) catalyzed intramolecular C-H insertion: α-substituents and conformational effects

Highly functionalized chiral γ-lactams are efficiently synthesized via Rh(II) catalyzed intramolecular C-H insertion from various α-diazoamides. Independent of α-substituents, regio- and stereoselectivities are enhanced through a conformational effect exerted by a bicyclic transition state.

New chiral auxiliaries based on conformation control, a C2-symmetric 2,2-dimethylimidazolidine and 4-chiral 2,2-dialkyloxazolidines. Synthesis and conformational analysis of acrylamide derivatives

New chirality-controlling auxiliaries, a C2-symmetric 2,2-dimethylimidazolidine and 4-chiral 2,2-dialkyloxazolidines, are readily prepared from a C2-symmetric 1,2-ethanediamine and naturally occurring α-amino acids, respectively. Con