-
1
-
-
0036817159
-
Synthesis of substituted piperidines via aziridinium intermediates: Synthetic applications
-
Cossy J, Gomez Pardo D. Synthesis of substituted piperidines via aziridinium intermediates: synthetic applications. Chemtracts 2002;15:579-605. (Pubitemid 35470690)
-
(2002)
Chemtracts
, vol.15
, Issue.11
, pp. 579-605
-
-
Cossy, J.1
Gomez Pardo, D.2
-
2
-
-
85016282057
-
Enantioselective ring expansion via aziridinium intermediates. Synthesis of substituted piperidines from substituted pyrrolidines. Synthetic applications
-
Cossy J, Gomez Pardo D. Enantioselective ring expansion via aziridinium intermediates. Synthesis of substituted piperidines from substituted pyrrolidines. Synthetic applications. Targets Heterocyclic Systems 2002;2:1-26.
-
(2002)
Targets Heterocyclic Systems
, vol.2
, pp. 1-26
-
-
Cossy, J.1
Gomez Pardo, D.2
-
4
-
-
0032811082
-
Ring expansion - Formation of optically active 3-hydroxypiperidines from pyrrolidinemethanol derivatives
-
Cossy J, Dumas C, Gomez Pardo D. Ring expansion - formation of optically active 3-hydroxypiperidines from pyrrolidinemethanol derivatives. Eur J Org Chem 1999;1693-1699.
-
(1999)
Eur J Org Chem
, pp. 1693-1699
-
-
Cossy, J.1
Dumas, C.2
Gomez Pardo, D.3
-
5
-
-
0034815682
-
Ring expansion: Synthesis of the velbanamine piperidine core
-
Cossy J, Mirguet O, Gomez Pardo D. Ring expansion: synthesis of the velbanamine piperidine core. Synlett 2001;1575-1577. (Pubitemid 32929762)
-
(2001)
Synlett
, Issue.10
, pp. 1575-1577
-
-
Cossy, J.1
Mirguet, O.2
Gomez Pardo, D.3
-
6
-
-
32444448756
-
Enantioselective diethylzinc addition to aromatic and aliphatic aldehydes using (3R,5R)-dihydroxypiperidine derivatives catalyst
-
DOI 10.1016/j.tet.2005.11.070, PII S0040402005021253
-
Roudeau R, Gomez Pardo D, Cossy J. Enantioselective diethylzinc addition to aromatic and aliphatic aldehydes using (3R,5R)-dihydroxypiperidine derivatives catalyst. Tetrahedron 2006;62:2388-2394. (Pubitemid 43227913)
-
(2006)
Tetrahedron
, vol.62
, Issue.10
, pp. 2388-2394
-
-
Roudeau, R.1
Gomez Pardo, D.2
Cossy, J.3
-
7
-
-
0031792973
-
A short and efficient synthesis of (3S,4S)-1-benzyl-4-N-benzylamino-3- hydroxypiperidine
-
Langlois N, Calvez O. A short and efficient synthesis of (3S,4S)-1-benzyl-4-N-benzylamino-3-hydroxypiperidine. Synth Commun 1998;28:4471-4477.
-
(1998)
Synth Commun
, vol.28
, pp. 4471-4477
-
-
Langlois, N.1
Calvez, O.2
-
8
-
-
33748845937
-
Synthesis of new chiral bicyclic 3-hydroxypiperidines - Highly diastereoselective ring expansion of the azabicyclo[3.3.0]octane system to chiral piperidine derivatives
-
Wilken J, Kossenjans M, Saak W, Haase D, Pohl S, Martens J. Synthesis of new chiral bicyclic 3-hydroxypiperidines - highly diastereoselective ring expansion of the azabicyclo[3.3.0]octane system to chiral piperidine derivatives. Liebigs Ann 1997;573-579.
-
(1997)
Liebigs Ann
, pp. 573-579
-
-
Wilken, J.1
Kossenjans, M.2
Saak, W.3
Haase, D.4
Pohl, S.5
Martens, J.6
-
9
-
-
0033600004
-
Solid-phase synthesis of a library of functionalized aminodiol scaffolds
-
Davis PW, Osgood SA, Hébert N, Sprankle KG, Swayze EE. Solid-phase synthesis of a library of functionalized aminodiol scaffolds. Biotechnol Bioeng 1999;61:143-154.
-
(1999)
Biotechnol Bioeng
, vol.61
, pp. 143-154
-
-
Davis, P.W.1
Osgood, S.A.2
Hébert, N.3
Sprankle, K.G.4
Swayze, E.E.5
-
10
-
-
18744403529
-
Stereoselective synthesis of 4-aminomethyl-3-hydroxyprolinols and ring expansion into enantiopure polyfunctionalized piperidines
-
Deyine A, Delcroix JM, Langlois N. Stereoselective synthesis of 4-aminomethyl-3-hydroxyprolinols and ring expansion into enantiopure polyfunctionalized piperidines. Heterocycles 2004;64:207-214.
-
(2004)
Heterocycles
, vol.64
, pp. 207-214
-
-
Deyine, A.1
Delcroix, J.M.2
Langlois, N.3
-
12
-
-
33746876014
-
Ring expansion of functionalized octahydroindoles to enantiopure cis-decahydroquinolines
-
DOI 10.1021/jo060592p
-
Mena M, Bonjoch J, Gomez Pardo D, Cossy J. Ring expansion of functionalized octahydroindoles to enantiopure cis-decahydroquinolines. J Org Chem 2006;71:5930-5935. (Pubitemid 44200260)
-
(2006)
Journal of Organic Chemistry
, vol.71
, Issue.16
, pp. 5930-5935
-
-
Mena, M.1
Bonjoch, J.2
Pardo, D.G.3
Cossy, J.4
-
14
-
-
0001820741
-
Synthesis of (-)-Pseudoconhydrine through Ring Enlargement of a L-Proline Derivative
-
Cossy J, Dumas C, Gomez Pardo D. Synthesis of (-)-pseudoconhydrine through ring enlargement of a L-proline derivative. Synlett 1997;905-906. (Pubitemid 127495127)
-
(1997)
Synlett
, vol.1997
, Issue.8
, pp. 905-906
-
-
Cossy, J.1
Dumas, C.2
Pardo, D.G.3
-
15
-
-
0032542168
-
Enantioselective synthesis of 2,3-disubstituted piperidines from (S)- Methylpyroglutamate
-
PII S004040399802190X
-
Calvez O, Chiaroni A, Langlois N. Enantioselective synthesis of 2,3-disubstituted piperidines from (S)-methyl pyroglutamate. Tetrahedron Lett 1998;39:9447-9450. (Pubitemid 28541102)
-
(1998)
Tetrahedron Letters
, vol.39
, Issue.51
, pp. 9447-9450
-
-
Calvez, O.1
Chiaroni, A.2
Langlois, N.3
-
16
-
-
0034696986
-
An easy access to 2,6-dihydroxy-9-azabicyclo[3.3.1]nonane, a versatile synthon
-
DOI 10.1021/jo991333l
-
Michel P, Rassat A. An easy acess to 2,6-dihydroxy-9-azabicyclo[3.3.1]- nonane, a versatile synthon. J Org Chem 2000;65:2572-2573. (Pubitemid 30235831)
-
(2000)
Journal of Organic Chemistry
, vol.65
, Issue.8
, pp. 2572-2573
-
-
Michel, P.1
Rassat, A.2
-
17
-
-
33846145139
-
Enantioselective ring expansion of prolinols and ring-closing metathesis: Formal synthesis of (-)-swainsonine
-
Déchamps I, Gomez Pardo D, Cossy J. Enantioselective ring expansion of prolinols and ring-closing metathesis: formal synthesis of (-)-swainsonine. Arkivoc 2007;v;38-45.
-
(2007)
Arkivoc
, vol.5
, pp. 38-45
-
-
Déchamps, I.1
Gomez Pardo, D.2
Cossy, J.3
-
18
-
-
34547581710
-
Enantioselective ring expansion of prolinol derivatives. Two formal synthesis of (-)-swainsonine
-
Déchamps I, Gomez Pardo D, Cossy J. Enantioselective ring expansion of prolinol derivatives. Two formal synthesis of (-)-swainsonine. Tetrahedron 2007;63:9082-9091.
-
(2007)
Tetrahedron
, vol.63
, pp. 9082-9091
-
-
Déchamps, I.1
Gomez Pardo, D.2
Cossy, J.3
-
19
-
-
0030803236
-
Synthesis and structure-activity relationships of 6,7-benzomorphan derivatives as antagonists of the NMDA receptor-channel complex
-
DOI 10.1021/jm970131j
-
Grauert M, Bechtel WD, Ensinger HA, Merz H, Carter AJ. Synthesis and structure-activity relationships of 6,7-benzomorphan derivatives as antagonists of the NMDA receptor-channel complex. J Med Chem 1997;40:2922-2930. (Pubitemid 27382543)
-
(1997)
Journal of Medicinal Chemistry
, vol.40
, Issue.18
, pp. 2922-2930
-
-
Grauert, M.1
Bechtel, W.D.2
Ensinger, H.A.3
Merz, H.4
Carter, A.J.5
-
20
-
-
0030743670
-
Synthesis of racemic 6,7,8,9-tetrahydro-3-hydroxy-1H-1-benzazepine-2,5- diones as antagonists of N-methyl-D-aspartate (NMDA) and α-amino-3- hydroxy-5-methylisoxazole-4-propionic acid (AMPA) receptors
-
Guzikowski AP, Whittemore ER, Woodward RM, Weber E, Keana JFW. Synthesis of racemic 6,7,8,9-tetrahydro-3-hydroxy-1H-1-benzazepine-2,5-diones as antagonists of N-methyl-D-aspartate (NMDA) and α-amino-3-hydroxy-5- methylisoxazole-4-propionic acid (AMPA) receptors. J Med Chem 1997;40:2424-2429.
-
(1997)
J Med Chem
, vol.40
, pp. 2424-2429
-
-
Guzikowski, A.P.1
Whittemore, E.R.2
Woodward, R.M.3
Weber, E.4
Keana, J.F.W.5
-
21
-
-
0033537680
-
Synthesis and photochemistry of a photolabile precursor of N-methyl-D- Aspartate (NMDA) that is photolyzed in the microsecond time region and is suitable for chemical kinetic investigations of the NMDA receptor
-
DOI 10.1021/bi9826557
-
Gee KR, Niu L, Schaper K, Jayaraman V, Hess GP. Synthesis and photochemistry of a photolabile precursor of N-methyl-D-aspartate (NMDA) that is photolyzed in the microsecond time region and is suitable for chemical kinetic investigations of NMDA receptor. Biochemistry 1999;38:3140-3147. (Pubitemid 29131822)
-
(1999)
Biochemistry
, vol.38
, Issue.10
, pp. 3140-3147
-
-
Gee, K.R.1
Niu, L.2
Schaper, K.3
Jayaraman, V.4
Hess, G.P.5
-
22
-
-
18744398256
-
Preparation of 4-[2-(piperidin-1-yl)ethanesulfonyl]-phenols as NMDA receptor-subtype selective blockers
-
2000;WO2000075109
-
Alanine A, Burner S, Buettelmann B, Heitz Neidhart MP, Jaeschke G, Pinard E, Wyler R. Preparation of 4-[2-(piperidin-1-yl)ethanesulfonyl]-phenols as NMDA receptor-subtype selective blockers. 2000;WO2000075109. Chem Abstr 2000;134:42064.
-
(2000)
Chem Abstr
, vol.134
, pp. 42064
-
-
Alanine, A.1
Burner, S.2
Buettelmann, B.3
Heitz Neidhart, M.P.4
Jaeschke, G.5
Pinard, E.6
Wyler, R.7
-
23
-
-
18744387550
-
Preparation of piperidine and piperazine compounds for use in the treatment of alzheimer
-
2001;EP1136475
-
Crameri Y, Scalone M, Waldmeier P, Widmer U. Preparation of piperidine and piperazine compounds for use in the treatment of alzheimer. 2001;EP1136475. Chem Abstr 2001;135:272882.
-
(2001)
Chem Abstr
, vol.135
, pp. 272882
-
-
Crameri, Y.1
Scalone, M.2
Waldmeier, P.3
Widmer, U.4
-
24
-
-
18744393548
-
Prodrugs to NMDA receptor ligands, namely phenolic esters of (3S,4S)-4-[2-(4-benzyl-3-hydroxypiperidin-1-yl) ethanesulfonyl]phenol, and their preparation and use
-
2002; WO 2002016321
-
Alanine A, Buettelmann B, Fisher H, Huwyler J, Heitz Neidhart MP, Jaeschke G, Pinard E, Wyler R. Prodrugs to NMDA receptor ligands, namely phenolic esters of (3S,4S)-4-[2-(4-benzyl-3-hydroxypiperidin-1-yl) ethanesulfonyl]phenol, and their preparation and use. 2002; WO 2002016321. Chem Abstr 2002;136:216649.
-
(2002)
Chem Abstr
, vol.136
, pp. 216649
-
-
Alanine, A.1
Buettelmann, B.2
Fisher, H.3
Huwyler, J.4
Heitz Neidhart, M.P.5
Jaeschke, G.6
Pinard, E.7
Wyler, R.8
-
25
-
-
0038384650
-
Efficient enantioselective synthesis of the NMDA 2B receptor antagonist Ro 67-8867
-
DOI 10.1021/op034006v
-
Scalone M, Waldmeier P. Efficient enantioselective synthesis of the NMDA 2B receptor antagonist Ro 67-8867. Org Proc Res Dev 2003;7:418-425. (Pubitemid 36706812)
-
(2003)
Organic Process Research and Development
, vol.7
, Issue.3
, pp. 418-425
-
-
Scalone, M.1
Waldmeier, P.2
-
26
-
-
18744366995
-
Efficient enantioselective formal synthesis of Ro 67-8867, a NMDA 2B receptor antagonist
-
DOI 10.1055/s-2005-865225, G04305ST
-
Déchamps I, Gomez Pardo D, Karoyan P, Cossy J. Efficient enantioselective formal synthesis of Ro 67-8867, a NMDA 2B receptor antagonist. Synlett 2005;1170-1172. (Pubitemid 40675953)
-
(2005)
Synlett
, Issue.7
, pp. 1170-1172
-
-
Dechamps, I.1
Pardo, D.G.2
Karoyan, P.3
Cossy, J.4
-
27
-
-
0031014620
-
New strategy for the synthesis of 3-substituted prolines
-
DOI 10.1016/S0040-4039(96)02221-6, PII S0040403996022216
-
Karoyan P; Chassaing G. New strategy for the synthesis of 3-substituted prolines. Tetrahedron Lett 1997;38:85-88. (Pubitemid 27018847)
-
(1997)
Tetrahedron Letters
, vol.38
, Issue.1
, pp. 85-88
-
-
Karoyan, P.1
Chassaing, G.2
-
28
-
-
0031014621
-
Zinca-ene-allene and zinc-enolate cyclization. Towards the synthesis of polysubstituted pyrrolidines
-
Lorthiois E, Marek I, Normant JF. Zinca-ene-allene and zinc-enolate cyclization. Towards the synthesis of polysubstituted pyrrolidines. Tetrahedron Lett 1997;38:89-92.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 89-92
-
-
Lorthiois, E.1
Marek, I.2
Normant, J.F.3
-
29
-
-
0030987385
-
Asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinomethionines: 3-Methylsulfanylmethyl-pyrrolidine-2-carboxylic acids
-
DOI 10.1016/S0957-4166(97)00203-6, PII S0957416697002036
-
Karoyan P, Chassaing G. Asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinomethionines: 3-(methylsulfanylmethyl)pyrrolidine-2-carboxylic acids. Tetrahedron Asymmetry 1997;8:2025-2032. (Pubitemid 27277927)
-
(1997)
Tetrahedron Asymmetry
, vol.8
, Issue.12
, pp. 2025-2032
-
-
Karoyan, P.1
Chassaing, G.2
-
30
-
-
0000541846
-
Diastereoselective and enantioselective intramolecular amino-zinc-enolate carbometalation reactions. a new polysubstituted pyrrolidines synthesis
-
Lorthiois E,Marek I, Normant JF. Diastereoselective and enantioselective intramolecular amino-zinc-enolate carbometalation reactions. A new polysubstituted pyrrolidines synthesis. J OrgChem 1998;63:2442-2450.
-
(1998)
J OrgChem
, vol.63
, pp. 2442-2450
-
-
Lorthiois, E.1
Marek, I.2
Normant, J.F.3
-
31
-
-
0037033192
-
Short asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinoglutamic acids: 2-carboxy-3-pyrrolidineacetic acids (CPAA)
-
Karoyan P, Chassaing G. Short asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinoglutamic acids: 2-carboxy-3-pyrrolidineacetic acids (CPAA). Tetrahedron Lett 2002;43:253-255.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 253-255
-
-
Karoyan, P.1
Chassaing, G.2
-
32
-
-
0037059970
-
Asymmetric synthesis of 3-alkyl substituted prolines by alkylation of a chiral sulfone
-
DOI 10.1016/S0040-4039(01)02391-7, PII S0040403901023917
-
Karoyan P, Chassaing G. Asymmetric synthesis of 3-alkyl substituted prolines by alkylation of a chiral sulfone. Tetrahedron Lett 2002;43:1221-1223. (Pubitemid 34127869)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.7
, pp. 1221-1223
-
-
Karoyan, P.1
Chassaing, G.2
-
33
-
-
0037459690
-
Amino-zinc-enolate carbometalation reactions: Application to ring closure of terminally substituted olefin for the asymmetric synthesis of cis- and trans-3-prolinoleucine
-
DOI 10.1021/jo026535n
-
Karoyan P, Quancard J, Vaissermann J, Chassaing G. Amino-zinc-enolate carbometalation reactions: application to ring closure of terminally substituted olefin for the asymmetric synthesis of cis- and trans-3-prolinoleucine. J Org Chem 2003;68:2256-2265. (Pubitemid 36505103)
-
(2003)
Journal of Organic Chemistry
, vol.68
, Issue.6
, pp. 2256-2265
-
-
Karoyan, Ph.1
Quancard, J.2
Vaissermann, J.3
Chassaing, G.4
-
34
-
-
1242272914
-
Amino-zincenolate cyclization: A short access to (2S,3R)- and (2S,3S)-3-benzylprolines (3-benzylpyrrolidine-2-carboxylic acids)
-
Quancard J, Magellan H, Lavielle S, Chassaing G, Karoyan P. Amino-zincenolate cyclization: a short access to (2S,3R)- and (2S,3S)-3-benzylprolines (3-benzylpyrrolidine-2-carboxylic acids). Tetrahedron Lett 2004;45:2185-2187.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 2185-2187
-
-
Quancard, J.1
Magellan, H.2
Lavielle, S.3
Chassaing, G.4
Karoyan, P.5
-
35
-
-
8644274669
-
Asymmetric synthesis of 3-substituted proline chimeras bearing polar side chains of proteinogenic amino acids
-
DOI 10.1021/jo048762q
-
Quancard J, Labonne A, Jacquot Y, Chassaing G, Lavielle S, Karoyan P. Asymmetric synthesis of 3-substituted proline chimeras bearing polar side chains of proteinogenic amino acids. J Org Chem 2004;69: 7940-7948. (Pubitemid 39507402)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.23
, pp. 7940-7948
-
-
Quancard, J.1
Labonne, A.2
Jacquot, Y.3
Chassaing, G.4
Lavielle, S.5
Karoyan, P.6
-
36
-
-
33750026643
-
Palladium- Or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formation
-
Negishi E. Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formation. Acc Chem Res 1982;15:340-348.
-
(1982)
Acc Chem Res
, vol.15
, pp. 340-348
-
-
Negishi, E.1
-
37
-
-
0010337731
-
Efficient synthesis of β- and γ-amino acid derivatives using new functionalised zinc reagents: Enhanced stability and reactivity of β-amido zinc reagents in dimethylformamide
-
Dexter CS, Jackson RFW. Efficient synthesis of β- and γ-amino acid derivatives using new functionalised zinc reagents: enhanced stability and reactivity of β-amido zinc reagents in dimethylformamide. J Chem Soc Chem Commun 1998;75-76. (Pubitemid 128686619)
-
(1998)
Chemical Communications
, Issue.1
, pp. 75-76
-
-
Dexter, C.S.1
Jackson, R.F.W.2
-
38
-
-
34247232142
-
2-symmetric tetraamine base
-
2-symmetric tetraamine base. Org Proc Res Dev 2007;11:215-222.
-
(2007)
Org Proc Res Dev
, vol.11
, pp. 215-222
-
-
Frizzle, M.J.1
Caille, S.2
Marshall, T.L.3
McRae, K.4
Nadeau, K.5
Guo, G.6
Wu, S.7
Martinelli, M.J.8
Moniz, G.A.9
-
39
-
-
33744725551
-
Aziridinium from N,N-dibenzyl serine methyl ester: Synthesis of enantiomerically pure β-amino and α,β-diamino esters
-
DOI 10.1021/ol060700u
-
Couturier C, Blanchet J, Schlama T, Zhu J. Aziridinium from N,N-dibenzyl serine methyl ester: synthesis of enantiomerically pure β-amino and α,β-diamino esters. Org Lett 2006;8:2183-2186. (Pubitemid 43823641)
-
(2006)
Organic Letters
, vol.8
, Issue.10
, pp. 2183-2186
-
-
Couturier, C.1
Blanchet, J.2
Schlama, T.3
Zhu, J.4
-
40
-
-
5144232796
-
Development of an efficient process for the preparation of Sch 39166: Aziridinium chemistry on scale
-
DOI 10.1021/op0402026
-
Gala D, Dahanukar VH, Eckert JM, Lucas BS, Schumacher DP, Zavialov IA, Buholzer P, Kubisch P, Mergelsberg I, Scherer D. Development of an efficient process for the preparation of Sch 39166: aziridinium chemistry on scale. Org Proc Res Dev 2004;8:754-768. (Pubitemid 39345689)
-
(2004)
Organic Process Research and Development
, vol.8
, Issue.5
, pp. 754-768
-
-
Gala, D.1
Dahanukar, V.H.2
Eckert, J.M.3
Lucas, B.S.4
Schumacher, D.P.5
Zavialov, I.A.6
Buholzer, P.7
Kubisch, P.8
Mergelsberg, I.9
Scherer, D.10
-
41
-
-
0037059483
-
Diamine synthesis: Exploring the regioselectivity of ring opening of aziridinium ions
-
DOI 10.1021/jo010824e
-
O'Brien P, Towers TD. Diamine synthesis: exploring the regioselectivity of ring opening of aziridinium ions. J Org Chem 2002;67:304-307. (Pubitemid 34052457)
-
(2002)
Journal of Organic Chemistry
, vol.67
, Issue.1
, pp. 304-307
-
-
O'Brien, P.1
Towers, T.D.2
-
42
-
-
0034624592
-
Treatment of N,N-dibenzylamino alcohols with sulfonyl chloride leads to rearranged β-chloro amines, precursors to β-amino acids, and not to tetrahydroisoquinolines
-
Weber K, Kuklinski S, Gmeiner P. Treatment of N,N-dibenzylamino alcohols with sulfonyl chloride leads to rearranged β-chloro amines, precursors to β-amino acids, and not to tetrahydroisoquinolines. Org Lett 2000;2:647-649.
-
(2000)
Org Lett
, vol.2
, pp. 647-649
-
-
Weber, K.1
Kuklinski, S.2
Gmeiner, P.3
-
43
-
-
0033575376
-
The preparation of β-substituted amines from mixtures of epoxide opening products via a common aziridinium ion intermediate
-
DOI 10.1016/S0957-4166(99)00243-8, PII S0957416699002438
-
Anderson SR, Ayers JT, DeVries KM, Ito F, Mendenhall D, Vanderplas BC. The preparation of β-substituted amines from mixtures of epoxide opening products via a common aziridinium ion intermediate. Tetrahedron Asymmetry 1999;10:2655-2663. (Pubitemid 29423373)
-
(1999)
Tetrahedron Asymmetry
, vol.10
, Issue.14
, pp. 2655-2663
-
-
Anderson, S.R.1
Ayers, J.T.2
Devries, K.M.3
Ito, F.4
Mendenhall, D.5
Vanderplas, B.C.6
-
44
-
-
0028104847
-
Enantiomerically pure amino alcohols and diamino alcohols from L-aspartic acid. Application to the synthesis of epi- and diepislaframine
-
DOI 10.1021/jo00101a042
-
Gmeiner P, Junge D, Kaertner A. Enantiomerically pure amino alcohols and diamino alcohols from L-aspartic acid. Application to the synthesis of epi- and diepislaframine. J Org Chem 1994;59:6766-6776. (Pubitemid 24356830)
-
(1994)
Journal of Organic Chemistry
, vol.59
, Issue.22
, pp. 6766-6776
-
-
Gmeiner, P.1
Junge, D.2
Kartner, A.3
-
45
-
-
0026572789
-
Stereo- and regioselective synthesis of chiral diamines and triamines from pseudoephedrine and ephedrine
-
Dieter RK, Deo N, Lagu B, Dieter JW. Stereo- and regioselective synthesis of chiral diamines and triamines from pseudoephedrine and ephedrine. J Org Chem 1992;57:1663-1671.
-
(1992)
J Org Chem
, vol.57
, pp. 1663-1671
-
-
Dieter, R.K.1
Deo, N.2
Lagu, B.3
Dieter, J.W.4
-
46
-
-
33747253554
-
Highly enantioselective synthesis of β-amino alcohols
-
DOI 10.1021/ol061133d
-
Métro TX, Appenzeller J, Gomez Pardo D, Cossy J. Highly enantioselective synthesis of β-amino alcohols. Org Lett 2006;8:3509-3512. (Pubitemid 44238338)
-
(2006)
Organic Letters
, vol.8
, Issue.16
, pp. 3509-3512
-
-
Metro, T.-X.1
Appenzeller, J.2
Pardo, D.G.3
Cossy, J.4
-
47
-
-
34547930152
-
Highly enantioselective synthesis of β-amino alcohols: A catalytic version
-
DOI 10.1021/jo071028x
-
Métro TX, Gomez Pardo D, Cossy J. Highly enantioselective synthesis of β-amino alcohols: a catalytic version. J Org Chem 2007;72:6556-6561. (Pubitemid 47267581)
-
(2007)
Journal of Organic Chemistry
, vol.72
, Issue.17
, pp. 6556-6561
-
-
Metro, T.-X.1
Pardo, D.G.2
Cossy, J.3
-
48
-
-
0021236980
-
Potential antidepressant agents. α-Aryloxy-benzyl derivatives of ethanolamine and morpholine
-
Melloni P, Carniel G, Della Torre A, Bonsignori A, Buonamici M, Pozzi O, Ricciardi S, Rossi AC. Potential antidepressant agents. α-Aryloxy-benzyl derivatives of ethanolamine and morpholine. Eur J Med Chem 1984;19:235-242. (Pubitemid 14075597)
-
(1984)
European Journal of Medicinal Chemistry
, vol.19
, Issue.3
, pp. 235-242
-
-
Melloni, P.1
Carniel, G.2
Della Torre, A.3
-
49
-
-
1642293910
-
The Selective Norepinephrine Reuptake Inhibitor Antidepressant Reboxetine: Pharmacological and Clinical Profile
-
Hajos M, Fleishaker JC, Filipiak-Reisner JK, Brown MT, Wong EHF. The selective norepinephrine reuptake inhibitor antidepressant reboxetine: pharmacological and clinical profile. CNS Drug Rev 2004; 10:23-44. (Pubitemid 38381173)
-
(2004)
CNS Drug Reviews
, vol.10
, Issue.1
, pp. 23-44
-
-
Hajos, M.1
Fleishaker, J.C.2
Filipiak-Reisner, J.K.3
Brown, M.T.4
Wong, E.H.F.5
-
50
-
-
15044347268
-
Highly selective norepinephrine reuptake inhibitors and method of using the same
-
2001;WO20010011973
-
Wong EHF, Ahmed S, Marshall RC, McArthur R, Taylor DP, Birgerson L, Cetera P. Highly selective norepinephrine reuptake inhibitors and method of using the same. 2001;WO20010011973. Chem Abstr 2001;134:105849.
-
(2001)
Chem Abstr
, vol.134
, pp. 105849
-
-
Wong, E.H.F.1
Ahmed, S.2
Marshall, R.C.3
McArthur, R.4
Taylor, D.P.5
Birgerson, L.6
Cetera, P.7
-
51
-
-
0022003362
-
Configurational studies on 2-[α-(2-ethoxyphenoxy)benzyl]morpholine FCE 20124
-
DOI 10.1016/S0040-4020(01)96541-X
-
Melloni P, Della Torre A, Lazzari E, Mazzini G, Meroni M. Configurational studies on 2-[α-(2-ethoxyphenoxy)benzyl]morpholine FCE 20124. Tetrahedron 1985;41:1393-1399. (Pubitemid 15123139)
-
(1985)
Tetrahedron
, vol.41
, Issue.7
, pp. 1393-1399
-
-
Melloni, P.1
Della Torre, A.2
Lazzari, E.3
-
52
-
-
1542336744
-
Chiral synthesis of (2S,3S)-2-(2-morpholin-2-yl-2-phenylmethoxy)phenol
-
Prabhakaran J, Majo VJ, Mann JJ, Kumar JSD. Chiral synthesis of (2S,3S)-2-(2-morpholin-2-yl-2-phenylmethoxy)phenol. Chirality 2004;16:168-173.
-
(2004)
Chirality
, vol.16
, pp. 168-173
-
-
Prabhakaran, J.1
Majo, V.J.2
Mann, J.J.3
Kumar, J.S.D.4
-
53
-
-
0035988975
-
Separation of reboxetine enantiomers by means of capillary electrophoresis
-
DOI 10.1002/1522-2683(200206)23:12<1870::AID-ELPS1870>3.0.CO;2-R
-
Raggi MA, Mandrioli R, Sabbioni C. Parenti C, Cannazza G, Fanali S. Separation of reboxetine enantiomers by means of capillary electrophoresis. Electrophoresis 2002;23:1870-1877. (Pubitemid 34752860)
-
(2002)
Electrophoresis
, vol.23
, Issue.12
, pp. 1870-1877
-
-
Raggi, M.A.1
Mandrioli, R.2
Sabbioni, C.3
Parenti, C.4
Cannazza, G.5
Fanali, S.6
-
54
-
-
19944432573
-
Discovery and structure-activity relationships of novel selective norepinephrine and dual serotonin/norepinephrine reuptake inhibitors
-
DOI 10.1016/j.bmcl.2004.11.025, PII S0960894X04013757
-
Boot J, Cases M, Clark BP, Findlay J, Gallagher PT, Hayhurst L, Man T, Montalbetti C, Rathmell RE, Rudyk H, Walter MW, Whatton M, Wood V. Discovery and structure-activity relationships of novel selective norepinephrine and dual serotonin/norepinephrine reuptake inhibitors. Biorg Med ChemLett 2005;15:699-703. (Pubitemid 40143150)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.3
, pp. 699-703
-
-
Boot, J.1
Cases, M.2
Clark, B.P.3
Findlay, J.4
Gallagher, P.T.5
Hayhurst, L.6
Man, T.7
Montalbetti, C.8
Rathmell, R.E.9
Rudyk, H.10
Walter, M.W.11
Whatton, M.12
Wood, V.13
-
55
-
-
0035080453
-
Direct separation of the enantiomers of reboxetine by liquid chromatography on different cellulose- and amylose-based chiral stationary phases
-
Ficarra R, Calabro ML, Tommasini S, Melardi S, Cutroneo P, Ficarra P. Direct separation of the enantiomers of reboxetine by liquid chromatography on different cellulose- and amylose-based chiral stationary phases. Chromatographia 2001;53:261-265. (Pubitemid 32245256)
-
(2001)
Chromatographia
, vol.53
, Issue.5-6
, pp. 261-265
-
-
Ficarra, R.1
Calabro, M.L.2
Tommasini, S.3
Melardi, S.4
Cutroneo, P.5
Ficarra, P.6
-
56
-
-
3242682430
-
Synthesis, enantiomeric resolution, and selective C-11 methylation of a highly selective radioligand for imaging the norepinephrine transporter with positron emission tomography
-
Lin KS, Ding YS. Synthesis, enantiomeric resolution, and selective C-11 methylation of a highly selective radioligand for imaging the norepinephrine transporter with positron emission tomography. Chirality 2004;16:475-481.
-
(2004)
Chirality
, vol.16
, pp. 475-481
-
-
Lin, K.S.1
Ding, Y.S.2
-
57
-
-
15044347050
-
Asymmetric synthesis of (+)-(S,S)-reboxetine via a new (S)-2-(hydroxymethyl)morpholine preparation
-
Benner E, Baldwin RM, Tamagan G. Asymmetric synthesis of (+)-(S,S)-reboxetine via a new (S)-2-(hydroxymethyl)morpholine preparation. Org Lett 2005;7:937-939.
-
(2005)
Org Lett
, vol.7
, pp. 937-939
-
-
Benner, E.1
Baldwin, R.M.2
Tamagan, G.3
-
58
-
-
39049149025
-
Process development for (S,S)-reboxetine succinate via a Sharpless asymmetric epoxidation
-
Henegar KE, Cebula M. Process development for (S,S)-reboxetine succinate via a Sharpless asymmetric epoxidation. Org Proc Res Dev 2007;11:354-358.
-
(2007)
Org Proc Res Dev
, vol.11
, pp. 354-358
-
-
Henegar, K.E.1
Cebula, M.2
-
59
-
-
22044439589
-
Enantioselective synthesis of (2R,3R)- and (2S,3S)-2-[(3-chlorophenyl)- (2-methoxyphenoxy)methyl]morpholine
-
Harding WW, Hodge M, Wang Z, Woolverton WL, Parrish D, Deschamps JR, Prisinzano TE. Enantioselective synthesis of (2R,3R)- and (2S,3S)-2-[(3- chlorophenyl)-(2-methoxyphenoxy)methyl]morpholine. Tetrahedron Asymmetry 2005;16:2249-2256.
-
(2005)
Tetrahedron Asymmetry
, vol.16
, pp. 2249-2256
-
-
Harding, W.W.1
Hodge, M.2
Wang, Z.3
Woolverton, W.L.4
Parrish, D.5
Deschamps, J.R.6
Prisinzano, T.E.7
-
60
-
-
70350528475
-
Preparation of norepinephrine transporter radiotracers
-
2007;WO 2007005935
-
Tamagan GD, Alagille D. Preparation of norepinephrine transporter radiotracers. 2007;WO 2007005935. Chem Abstr 146:121754, 2007.
-
(2007)
Chem Abstr
, vol.146
, pp. 121754
-
-
Tamagan, G.D.1
Alagille, D.2
-
61
-
-
33746288669
-
Enantioselective synthesis of (+)-(S,S)-reboxetine
-
Siddiqui SA, Narkhede UC, Lahoti RJ, Srinivasan KV. Enantioselective synthesis of (+)-(S,S)-reboxetine. Synlett 2006;1771-1773.
-
(2006)
Synlett
, pp. 1771-1773
-
-
Siddiqui, S.A.1
Narkhede, U.C.2
Lahoti, R.J.3
Srinivasan, K.V.4
-
62
-
-
40949130375
-
Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of β-amino alcohols
-
Mé tro TX, Gomez Pardo D, Cossy J. Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of β-amino alcohols. J Org Chem 2008;73:707-710.
-
(2008)
J Org Chem
, vol.73
, pp. 707-710
-
-
Métro, T.X.1
Gomez Pardo, D.2
Cossy, J.3
|