(2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide

Base Information

Chemical Name:(2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide
CAS No.:1073146-94-7
Molecular Formula:C₂₃H₂₈N₂O₂S
Molecular Weight:396.554
Hs Code.:

Synonyms:(2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide

Suppliers and Price of (2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide

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 (2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide

There total 1 articles about (2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide 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: 57.0%

: 440084-60-6
2-methylene-cyclopropanecarboxylic acid diethylamide

: 153277-49-7
(S)-N-benzylidene-4-toluenesulfinamide

: 1073146-94-7
(2R,3R)-4-methylene-2-phenyl-1-((S)-toluene-4-sulfinyl)-pyrrolidine-3-carboxylic acid diethylamide

Guidance literature:: With magnesium iodide; In tetrahydrofuran; at 20 ℃; for 3.33333h; stereoselective reaction; Inert atmosphere; Reflux;
DOI:10.1021/jo802049u