856410-06-5

Upstream product

• 856410-04-3 1-ethyl 4-methyl 2-trichloroacetylamino-3-methylidenebutanedioate 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 856410-05-4 1-ethyl 4-methyl 2-trichloroacetiminoxy-3-methylidenebutanedioate 
• 856410-03-2 1-ethyl 4-methyl 2-trichloroacetylaminocarbonyloxy-3-methylenebutandioate 
• 108735-94-0 1-Ethyl 4-methyl 2-hydroxy 3-methylenebutanedioate 

Downstream Products

• 856410-08-7 (3S,4R,1'S)-3-t-butoxycarbonylamino-4-hydroxymethyl-1-(1'-phenylethyl)pyrrolidin-2-one 
• 856410-12-3 (3S,4R,1S')-3-t-butoxycarbonylamino-4-methoxycarbonyl-1-(1'-phenylethyl)pyrrolidin-2-one 
• 856410-09-8 (3S,4R,1'S)-3-t-butoxycarbonylamino-1-(1'-phenyl-ethyl)-4-(tetrahydropyran-2-yloxymethyl)pyrrolidin-2-one 
• 1206626-18-7 (3S,4R,1'S)-4-benzyl-4-methoxycarbonyl-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-19-8 (3S,4S,1'S)-4-benzyl-4-methoxycarbonyl-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-16-5 (3S,4R,1'S)-4-allyl-4-methoxycarbonyl-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-17-6 (3S,4S,1'S)-4-allyl-4-methoxycarbonyl-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-12-1 (3S,4R,1'S)-4-methoxycarbonyl-4-methyl-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-13-2 (3S,4S,1'S)-4-methoxycarbonyl-4-methyl-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-14-3 (3S,4R,1'S)-4-methoxycarbonyl-4-(2''-methylprop-1''-yl)-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 
• 1206626-15-4 (3S,4S,1'S)-4-methoxycarbonyl-4-(2''-methylprop-1''-yl)-1-(1'-phenyleth-1'-yl)-3-trichloroacetylaminopyrrolidin-2-one 

Relevant academic research and scientific papers

Conformationally restricted analogues of both (S)-β-homoserine and (S)-aspartic acid from chiral 3-acylamino pyrrolidin-2-ones

Starting from chiral 3,4-trans-disubstituted pyrrolidin-2-ones 11a and 11b, obtained from a Baylis-Hillman adduct, conformationally restricted analogues of both (S)-β-homoserine, 17, and (S)-aspartic acid, 21, were synthesized, respectively, and these com

NEW SYNTHONS FOR THE SYNTHESIS OF CHIRAL PEPTIDE NUCLEIC ACIDS AND METHODS FOR PREPARING THE SAME

Novel l-acyl-3-amino-4-hydroxymethylpyiτolidine derivatives useful as PNA synthons optionally having protecting groups suitable of removal under mild conditions are disclosed having the formula (E) wherein: R1 is H or R-C(=O), wherein R is stra