trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate

Base Information

Chemical Name:trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate
CAS No.:1322877-80-4
Molecular Formula:C₂₂H₂₁ClN₂O₈
Molecular Weight:476.87
Hs Code.:

Synonyms:trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate

Suppliers and Price of trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate

There total 1 articles about trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate 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: 95.0%

: 555-16-8
4-nitrobenzaldehdye

: 624-48-6
dimethyl cis-but-2-ene-1,4-dioate

: 141109-14-0,141109-16-2,141109-13-9
2-(2-chlorophenyl)glycine methyl ester hydrochloride

: 1322877-80-4
trimethyl (2S,3S,4R,5S)-2-(2-chlorophenyl)-5-(4-nitrophenyl)pyrrolidine-2,3,4-tricarboxylate

Guidance literature:: With C₄₂H₂₈O₉P₂; In chloroform; at 50 ℃; for 54h; optical yield given as %ee; enantioselective reaction; Molecular sieve;
DOI:10.1021/ja204218h