299207-23-1

Upstream product

• 107-21-1 ethylene glycol 
• 59830-61-4 (S)-(1-benzyl-2,2-dimethoxyethyl)carbamic acid benzyl ester 
• 59830-60-3 benzyl (1S)-(1-formyl-2-phenylethyl)carbamate 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 114744-85-3 [(S)-1-(methoxy-methyl-carbamoyl)-2-phenyl-ethyl]-carbamic acid benzyl ester 
• 501-53-1 benzyl chloroformate 
• 1161-13-3 N-Cbz-L-Phe 
• 6372-14-1 N-((benzyloxy)carbonyl)-L-phenylalaninol 
• 3182-95-4 L-Phenylalaninol 

Downstream Products

• 611210-34-5 (2S)-N-[(1S)-1-(1,3-dioxolan-2-yl)-2-phenylethyl]-2-hydroxy-3-methylbutanamide 
• 611210-30-1 (2S)-N-[(1S)-1-(1,3-dioxolan-2-yl)-2-phenylethyl]-2-hydroxy-4-methylpentanamide 
• 611210-36-7 (2S)-N-[(1S)-1-(1,3-dioxolan-2-yl)-2-phenylethyl]-2-hydroxy-3-phenylpropanamide 
• 114701-13-2 (2S,3S)-2-Benzyl-3-(2-hydroxy-ethoxy)-5-methylene-piperidine-1-carboxylic acid methyl ester 
• 114724-30-0 ((S)-1-[1,3]Dioxolan-2-yl-2-phenyl-ethyl)-(2-trimethylsilanylmethyl-allyl)-carbamic acid methyl ester 
• 114701-05-2 (1S)-1-(1,3-dioxolan-2-yl)-2-phenylethanamine 

Relevant academic research and scientific papers

HYDROXYMORPHOLINONE DERIVATIVE AND MEDICINAL USE THEREOF

A compound represented by the following formula (I) wherein R1 and R2 are each a lower alkyl group optionally having substituents, which has a calpain inhibitory activity, or a salt thereof is provided.

Novel 6-Hydroxy-3-morpholinones as cornea permeable calpain inhibitors

A novel series of 6-hydroxy-3-morpholinones, in which the functional aldehyde and the hydroxy group of P2 site form a cyclic hemiacetal, was identified as calpain inhibitors. The placement of isobutyl group at the 2-position of the 3-morpholino

Solid-phase synthesis of C-terminal peptide aldehydes from amino acetals anchored to a backbone amide linker (BAL) handle

Peptide aldehydes were synthesized, starting from amino acetals, by a Solid-phase backbone amide linker (BAL) strategy. (C) 2000 Elsevier Science Ltd.

DIASTEREOSELECTIVE SYNTHESIS OF 2,3-CIS-2-ALKYL-3-OXYGENATED PIPERIDINE DERIVATIVES BY TITANIUM MEDIATED INTRAMOLECULAR CYCLIZATION OF α-AMINOACETAL-ALLYLSILANE SYSTEM

(2S,3S)-2-Alkyl-3-oxygenated 5-methylenepiperidines were obtained with high diastereoselectivity by cyclization of N-methoxycarbonyl-N-silylmethallyl-α-alkylaminoacetaldehyde ethyleneacetals with TiCl3(OPri).