(S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

Base Information

Chemical Name:(S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate
CAS No.:1197132-40-3
Molecular Formula:C₂₇H₂₅ClNO₄PS
Molecular Weight:525.993
Hs Code.:

Synonyms:(S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

Suppliers and Price of (S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

Supply Marketing:

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

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Total 2 raw suppliers

Chemical Property of (S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of (S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

There total 1 articles about (S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate 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:

: 87751-37-9
N-(4-chlorobenzylidene)benzenesulfonamide

: 880335-39-7
benzyl benzyl-H-phosphinate

: (R)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

: (S)-benzyl benzyl((S)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

: 1197132-40-3
(S)-benzyl benzyl((R)-(4-chlorophenyl)(phenylsulfonamido)methyl)phosphinate

Guidance literature:: With (1S,2S)-N-(dipyrrolidin-1-ylmethylene)-2-(dipyrrolidin-1-ylmethylenamino)-1,2-diphenylethanaminium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate; potassium carbonate; In dichloromethane; toluene; at -40 ℃; for 108h; optical yield given as %ee; enantioselective reaction;
DOI:10.1002/anie.200903971