cas 201855-60-9, trans 1-Benzyl-4-(4-fluorophenyl)-3-piperidinemethanol | Articles data ｜lookchem

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201855-60-9

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Articles about 201855-60-9Total 10 be found

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Multigram-scale flow synthesis of the chiral key intermediate of (-)-paroxetine enabled by solvent-free heterogeneous organocatalysis
10.1039/c9sc04752b
?tv?s, Sándor B.,Pericàs, Miquel A.,Kappe, C. Oliver
p. 11141 - 11146
(2019/12/28)

Catalytic Michael/Ring-Closure Reaction of α,β-Unsaturated Pyrazoleamides with Amidomalonates: Asymmetric Synthesis of (?)-Paroxetine
10.1002/chem.201603056
Zhang, Yu,Liao, Yuting,Liu, Xiaohua,Yao, Qian,Zhou, Yuhang,Lin, Lili,Feng, Xiaoming
p. 15119 - 15124
(2016/10/11)

Optically pure γ-butyrolactones and epoxy esters via two stereocentered HKR of 3-substituted epoxy esters: A formal synthesis of (-)-paroxetine, Ro 67-8867 and (+)-eldanolide
10.1039/c3ob27321k
Devalankar, Dattatray A.,Karabal, Pratibha U.,Sudalai, Arumugam
supporting information
p. 1280 - 1285
(2013/05/08)

Highly enantioselective organocatalytic cascade reaction for the synthesis of piperidines and oxazolidines
10.1016/j.tet.2011.08.079
?íhalová, Sylva,Valero, Guillem,Schimer, Ji?í,Humpl, Marek,Dra?ínsky, Martin,Moyano, Albert,Rios, Ramon,Vesely, Jan
scheme or table
p. 8942 - 8950
(2011/12/01)

Stereospecific construction of substituted piperidines. Synthesis of (-)-paroxetine and (+)-laccarin
10.1039/b617260a
Bower, John F.,Riis-Johannessen, Thomas,Szeto, Peter,Whitehead, Andrew J.,Gallagher, Timothy
p. 728 - 730
(2007/10/03)

Organocatalytic conjugate addition of malonates to α,β- unsaturated aldehydes: Asymmetric formal synthesis of (-)-paroxetine, chiral lactams, and lactones
10.1002/anie.200601025
Brandau, Sven,Landa, Aitor,Franzen, Johan,Marigo, Mauro,Jorgensen, Karl Anker
p. 4305 - 4309
(2007/10/03)

Concise synthesis of trans- and cis-3,4-disubstituted piperidines based on regio- and stereoselective allylation of cyclopentenyl esters
10.1016/j.tetlet.2004.08.174
Igarashi, Junji,Ishiwata, Hiroyuki,Kobayashi, Yuichi
p. 8065 - 8068
(2007/10/03)

Application of the chiral base desymmetrisation of imides to the synthesis of the alkaloid jamtine and the antidepressant paroxetine
10.1016/j.tet.2003.08.046
Gill, Christopher D.,Greenhalgh, Daniel A.,Simpkins, Nigel S.
p. 9213 - 9230
(2007/10/03)

A formal synthesis of (-)-paroxetine by enantioselective ring enlargement of a trisubstituted prolinol
10.1002/1099-0690(200211)2002:21<3543::AID-EJOC3543>3.0.CO;2-0
Cossy, Janine,Mirguet, Olivier,Pardo, Domingo Gomez,Desmurs, Jean-Roger
p. 3543 - 3551
(2007/10/03)

Ring expansion: Formal total synthesis of (-)-paroxetine
10.1016/S0040-4039(01)01096-6
Cossy, Janine,Mirguet, Olivier,Gomez Pardo, Domingo,Desmurs, Jean-Roger
p. 5705 - 5707
(2007/10/03)

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Chemical Properties

Melting Point: >55oC (dec.)
Boiling Point: 402.1oC at 760 mmHg
Flash Point:197oC
Density: 1.139g/cm3
Solubility:Chloroform (Slightly), DMSO (Slightly)
Storage Temp.:-20°C, Inert atmosphere
Vapor Pressure: 3.45E-07mmHg at 25°C
PSA: 23.47000
LogP: 3.36160

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