127927-60-0

Upstream product

• 341524-38-7 (-)-(2S,1'S)-1-benzyl-2-[1'-(dibenzylamino)-2'-(phenyl)ethyl]aziridine 
• 127943-39-9 (1R)-[1'(S)-(dibenzylamino)-2'-phenylethyl]oxirane 
• 100-46-9 benzylamine 
• 127927-43-9 Dibenzyl-((S)-1-oxiranyl-2-phenyl-ethyl)-amine 

Relevant academic research and scientific papers

Ring opening of nonactivated 2-(1-aminoalkyl) aziridines: Unusual regio- and stereoselective C-2 and C-3 cleavage

We have studied the ring opening of nonactivated amino aziridines 1 by water under acidic conditions. Depending on the acid used, amino aziridines are cleaved at C-3 or C-2 with high regioselectivity, and total stereoselectivity, affording chiral 2,3-diam

PROTECTIVE GROUP TUNING IN THE STEREOSELECTIVE CONVERSION OF α-AMINO ALDEHYDES INTO AMINOALKYL EPOXIDES

Sulfonium and arsonium ylides of the type CH2=S(CH3)2 and CH2=As(Ph)3 react with doubly protected α-amino aldehydes 1 derived from amino acids to form aminoalkyl epoxides 3/4, diastereofacial selectivity ranging between 86:14 and >95:5.