(2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

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Chemical Name:(2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam
CAS No.:474882-23-0
Molecular Formula:C₂₄H₃₁NO₄S
Molecular Weight:429.58
Hs Code.:

Synonyms:(2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

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Chemical Property of (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

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Technology Process of (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

There total 1 articles about (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam 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: 88.0%

: 14371-10-9
(E)-3-phenylpropenal

: 127392-82-9
1-((3aS,6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)pent-4-en-1-one

: 474882-23-0
(2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

Guidance literature:: 1-((3aS,6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-1H-3a,6-methanobenzo[c]isothiazol-1-yl)pent-4-en-1-one; With N-ethyl-N,N-diisopropylamine; diethylboron trifluoromethanesulfonate; In hexane; dichloromethane; at -5 ℃; for 0.333333h;

(E)-3-phenylpropenal; In hexane; dichloromethane; at -78 ℃; for 2h;
DOI:10.1081/CAR-120003734

Reference yield:

: 474882-23-0
(2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

: (1R,2R,3R,4S)-4-hydroxymethyl-1,2,3-trihydroxycyclopentane

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / RuCl₂(=CHPh)(PCy₃)2 / CH₂Cl₂

2: 90 percent / K₂OsO₄*2H₂O; N-methylmorpholine N-oxide / 2-methyl-propan-2-ol; dimethylformamide / 20 °C

3: 52 percent / NaBH₄ / ethanol / 1 h / 20 °C

With Grubbs catalyst first generation; sodium tetrahydroborate; potassium osmate(VI); 4-methylmorpholine N-oxide; In ethanol; dichloromethane; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1081/CAR-120003734