(1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol

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Chemical Name:(1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol
CAS No.:1127306-32-4
Molecular Formula:C₂₁H₂₂N₂O₆S
Molecular Weight:430.481
Hs Code.:

Synonyms:(1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol

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Chemical Property of (1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol

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Technology Process of (1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol

There total 1 articles about (1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol 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:

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Reference yield:

: 1127305-35-4
(Z)-(1'R,4'R,1''R)-N-{4'-[diisopropyl(1''-phenylallyloxy)silyloxy]cyclopent-2'-en-1'-yl}-N-{4-[2-((N'-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-4-methylbenzenesulfonamido)methylallyloxy]but-2-enyl}-2-nitrobenzenesulfonamide

: 1127306-32-4
(1S,2Z,4R)-1-phenyl-5-[(2R)-1'-(2-nitrophenylsulfonyl)-2,5-dihydro-1H-pyrrol-2-yl]-pent-2-ene-1,4-diol

Guidance literature:: (Z)-(1'R,4'R,1''R)-N-{4'-[diisopropyl(1''-phenylallyloxy)silyloxy]cyclopent-2'-en-1'-yl}-N-{4-[2-((N'-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)-4-methylbenzenesulfonamido)methylallyloxy]but-2-enyl}-2-nitrobenzenesulfonamide; With Grubbs catalyst first generation; In dichloromethane; Inert atmosphere; Reflux;

With tris(hydroxymethyl)phosphine; triethylamine; In dichloromethane; at 20 ℃; for 0.25h; Further stages; Inert atmosphere;
DOI:10.1002/anie.200804486