(2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

Base Information

Chemical Name:(2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate
CAS No.:1403165-21-8
Molecular Formula:C₃₀H₂₇N₃O₆S
Molecular Weight:557.627
Hs Code.:

Synonyms:(2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

Suppliers and Price of (2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

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Technology Process of (2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

There total 1 articles about (2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 886209-14-9
C₁₄H₁₂N₂O₄S

: 81167-39-7
methyl N-(diphenylmethylene)glycinate

: 1403164-85-1
(2S,3R)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

: (2R,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

: 1403165-21-8
(2S,3S)-methyl 2-(diphenylmethyleneamino)-3-(4-nitrophenylsulfonamido)-3-p-tolylpropanoate

Guidance literature:: With 2,6-bis((2R,4S,5S)-1-benzyl-4,5-diphenylimidazolidin-2-yl)pyridine; copper(II) bis(trifluoromethanesulfonate); N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 ℃; for 35h; Overall yield = 43 %; stereoselective reaction; Inert atmosphere;
DOI:10.1002/chem.201201537