93267-06-2

Upstream product

• 50299-15-5 methyl (S)-allylglycinate 
• 98-59-9 p-toluenesulfonyl chloride 
• 16338-48-0 L-allylglycine 
• 17234-07-0 ester methylique de la N,O-ditosyl L-serine 
• 917-57-7 vinyllithium 
• 93380-04-2 ester methylique de la N-tosyl β-iodo L-alanine 
• 67-56-1 methanol 
• 110579-31-2 (2S)-N-para-toluenesulfonylvinylglycine 

Downstream Products

• 282527-05-3 (S)-2-[(1-Benzyloxy-allyl)-(toluene-4-sulfonyl)-amino]-pent-4-enoic acid methyl ester 
• 305836-74-2 methyl (L)-N-allyl-N'-tosylallylglycinate 
• 1138019-25-6 methyl (2S)-2-((3-methylbutyl)(4-methylphenylsulfonyl)amino)pent-4-enoate 
• 178389-47-4 S-2-[N-(toluene-4-sulfonyl)-N-(3-phenylprop-2-ynyl)amino]-pent-4-enoic acid methyl ester 
• 178389-44-1 (3S-(3α,4aα))-6-oxo-2-(toluene-4-sulfonyl)-2,3,4,4a,5,6-hexahydro-1H-[2]pyrindine-3-carboxylic acid methyl ester 
• 282527-07-5 (S)-6-Benzyloxy-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydro-pyridine-2-carboxylic acid methyl ester 
• 252648-34-3 (2S,3aR)-5-Oxo-1-(toluene-4-sulfonyl)-1,2,3,3a,4,5-hexahydro-cyclopenta[b]pyrrole-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Stereospecific synthesis of chiral N-(ethynyl)allylglycines and their use in highly stereoselective intramolecular Pauson-Khand reactions

The first synthesis of an enantiopure N-ethynylated allylglycine and its application in the intramolecular Pauson-Khand reaction, which leads to a novel highly functionalised proline derivative with complete control of stereoselectivity, is reported.

LES ORGANOCUPRATES DANS UNE NOUVELLE SYNTHESE D'AMINOACIDES ENANTIOMERIQUEMENT PURS

A new general method of synthesis of optically pure α- amino esters was elaborated during studies on the reaction of organocuprates with tosyl and halogeno derivatives of L-serine and L-homoserine.