-
1
-
-
0026810813
-
Pyrrole, pyrrolidine, piperidine, pyridine, and azepine alkaloids
-
Pinder, A. R. Pyrrole, pyrrolidine, piperidine, pyridine, and azepine alkaloids Nat. Prod. Rep. 1992, 9, 17-23
-
(1992)
Nat. Prod. Rep.
, vol.9
, pp. 17-23
-
-
Pinder, A.R.1
-
2
-
-
4644296823
-
History, chemistry and biology of alkaloids from Lobelia inflata
-
DOI 10.1016/j.tet.2004.08.010, PII S0040402004012943
-
Felpin, F. X.; Lebreton, J. History, chemistry and biology of alkaloids from Lobelia inflata Tetrahedron 2004, 60, 10127-10153 (Pubitemid 39303964)
-
(2004)
Tetrahedron
, vol.60
, Issue.45
, pp. 10127-10153
-
-
Felpin, F.-X.1
Lebreton, J.2
-
3
-
-
38549126119
-
Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework
-
DOI 10.1016/j.bmc.2007.10.018, PII S096808960700884X
-
Källstrom, S.; Leino, R. Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework Bioorg. Med. Chem. 2008, 16, 601-635 (Pubitemid 351163050)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.2
, pp. 601-635
-
-
Kallstrom, S.1
Leino, R.2
-
4
-
-
0033775563
-
Catalytic imino Diels-Alder reaction by triflic imide and its application to one-pot synthesis from three components
-
O'Hagan, D. Catalytic imino Diels-Alder reaction by triflic imide and its application to one-pot synthesis from three components Nat. Prod. Rep. 2000, 17, 435-446
-
(2000)
Nat. Prod. Rep.
, vol.17
, pp. 435-446
-
-
O'Hagan, D.1
-
5
-
-
14744305091
-
The chemistry and pharmacology of tetrahydropyridines
-
Mateeva, N. N.; Winfield, L. L.; Redda, K. K. The chemistry and pharmacology of tetrahydropyridines Curr. Med. Chem. 2005, 12, 551-571 (Pubitemid 40331051)
-
(2005)
Current Medicinal Chemistry
, vol.12
, Issue.5
, pp. 551-571
-
-
Mateeva, N.N.1
Winfield, L.L.2
Redda, K.K.3
-
6
-
-
84896786886
-
-
JP Patent 61035788.
-
Komoto, T.; Yano, K.; Ono, J.; Okawa, J.; Nakajima, T. JP Patent 61035788, 1986.
-
(1986)
-
-
Komoto, T.1
Yano, K.2
Ono, J.3
Okawa, J.4
Nakajima, T.5
-
7
-
-
0028099645
-
Diastereoselective [4 + 2] type cycloaddition of 1-azatriene iron-tricarbonyl complex: Asymmetric synthesis of a piperidine alkaloid
-
Takemoto, Y.; Ueda, S.; Takeuchi, J.; Nakamoto, T.; Iwata, C. Diastereoselective [4 + 2] type cycloaddition of 1-azatriene iron-tricarbonyl complex: Asymmetric synthesis of a piperidine alkaloid Tetrahedron Lett. 1994, 35, 8821-8824
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 8821-8824
-
-
Takemoto, Y.1
Ueda, S.2
Takeuchi, J.3
Nakamoto, T.4
Iwata, C.5
-
8
-
-
0030902238
-
Antiviral properties of palinavir, a potent inhibitor of the human immunodeficiency virus type 1 protease
-
Lamarre, D.; Croteau, G.; Bourgon, L.; Thibeault, D.; Wardrop, E.; Clouette, C.; Vaillancourt, M.; Cohen, E.; Pargellis, C.; Yoakim, C.; Anderson, P. Antiviral properties of palinavir, A potent inhibitor of the human immunodeficiency virus type 1 protease Antimicrob. Agents Chemother. 1997, 41, 965-971 (Pubitemid 27194169)
-
(1997)
Antimicrobial Agents and Chemotherapy
, vol.41
, Issue.5
, pp. 965-971
-
-
Lamarre, D.1
Croteau, G.2
Wardrop, E.3
Bourgon, L.4
Thibeault, D.5
Clouette, C.6
Vaillancourt, M.7
Cohen, E.8
Pargellis, C.9
Yoakim, C.10
Anderson, P.C.11
-
10
-
-
0343228906
-
-
U.S. Patent 5,614,533.
-
Anderson, P. C.; Soucy, F.; Yoakim, C.; Lavallee, P.; Beaulieu, P. L. Substituted pipecolinic acid derivatives as HIV protease inhibitors. U.S. Patent 5,614,533, 1997.
-
(1997)
Substituted Pipecolinic Acid Derivatives As HIV Protease Inhibitors
-
-
Anderson, P.C.1
Soucy, F.2
Yoakim, C.3
Lavallee, P.4
Beaulieu, P.L.5
-
11
-
-
0035185180
-
Demographic and therapeutic determinants of pain reactivity in very low birth weight neonates at 32 weeks' postconceptional age
-
Pelham, W. E.; Gnagy, E. M.; Burrows-Maclean, L.; Williams, A.; Fabiano, G. A.; Morrisey, S. M.; Chronis, A. M.; Forehand, G. L.; Nguyen, C. A.; Hoffman, M. T.; Lock, T. M.; Fielbelkorn, K.; Coles, E. K.; Panahon, C. J.; Steiner, R. L.; Meichenbaum, D. L.; Onyango, A. N.; Morse, G. D. Demographic and therapeutic determinants of pain reactivity in very low birth weight neonates at 32 weeks' postconceptional age Pediatrics 2001, 107, 105-112
-
(2001)
Pediatrics
, vol.107
, pp. 105-112
-
-
Pelham, W.E.1
Gnagy, E.M.2
Burrows-Maclean, L.3
Williams, A.4
Fabiano, G.A.5
Morrisey, S.M.6
Chronis, A.M.7
Forehand, G.L.8
Nguyen, C.A.9
Hoffman, M.T.10
Lock, T.M.11
Fielbelkorn, K.12
Coles, E.K.13
Panahon, C.J.14
Steiner, R.L.15
Meichenbaum, D.L.16
Onyango, A.N.17
Morse, G.D.18
-
12
-
-
0028332094
-
Survey on the pharmacodynamics of the new antipsychotic risperidone
-
Megens, A. A. H. P.; Awouters, F. H. L.; Schotte, A.; Meert, T. F.; Dugovic, C.; Niemegeers, C. J. E.; Leysen, J. E. Survey on the pharmacodynamics of the new antipsychotic risperidone Psychopharmacology 1994, 114, 9-23 (Pubitemid 24150515)
-
(1994)
Psychopharmacology
, vol.114
, Issue.1
, pp. 9-23
-
-
Megens, A.A.H.P.1
Awouters, F.H.L.2
Schotte, A.3
Meert, T.F.4
Dugovic, C.5
Niemegeers, C.J.E.6
Leysen, J.E.7
-
13
-
-
37449030577
-
Risperidone, haloperidol, and placebo in the treatment of aggressive challenging behaviour in patients with intellectual disability: A randomised controlled trial
-
Tyrer, P.; Oliver-Africano, P. C.; Ahmed, Z.; Bouras, N.; Cooray, S.; Deb, S.; Murphy, D.; Hare, M.; Meade, M.; Reece, B.; Kramo, K.; Bhaumik, S.; Harley, D.; Regan, A.; Thomas, D.; Rao, B.; North, B.; Eliahoo, J.; Karatela, S.; Soni, A.; Crawford, M. Risperidone, haloperidol, and placebo in the treatment of aggressive challenging behaviour in patients with intellectual disability: A randomised controlled trial Lancet 2008, 371, 57-63
-
(2008)
Lancet
, vol.371
, pp. 57-63
-
-
Tyrer, P.1
Oliver-Africano, P.C.2
Ahmed, Z.3
Bouras, N.4
Cooray, S.5
Deb, S.6
Murphy, D.7
Hare, M.8
Meade, M.9
Reece, B.10
Kramo, K.11
Bhaumik, S.12
Harley, D.13
Regan, A.14
Thomas, D.15
Rao, B.16
North, B.17
Eliahoo, J.18
Karatela, S.19
Soni, A.20
Crawford, M.21
more..
-
14
-
-
0032926540
-
The effects of donepezil in Alzheimer's disease - Results from a multinational trial
-
DOI 10.1159/000017126
-
Burns, A.; Rossor, M.; Hecker, J.; Gauthier, S.; Petit, H.; Mçller, H. J.; Rogers, S. L.; Friedhoff, L. T. The effects of donepezil in Alzheimer's disease: Results from a multinational trial Dementia Geriatr. Cognit. Disord. 1999, 10, 237-244 (Pubitemid 29224502)
-
(1999)
Dementia and Geriatric Cognitive Disorders
, vol.10
, Issue.3
, pp. 237-244
-
-
Burns, A.1
Rossor, M.2
Hecker, J.3
Gauthier, S.4
Petit, H.5
Moller, H.-J.6
Rogers, S.L.7
Friedhoff, L.T.8
-
15
-
-
34248185107
-
Synthesis, stereochemistry and antimicrobial evaluation of t(3)-benzyl-r(2),c(6)-diarylpiperidin-4-one and its derivatives
-
DOI 10.1016/j.ejmech.2006.11.009, PII S0223523406004296
-
Jayabharathi, J.; Manimekalai, A.; Consalata Vani, T.; Padmavathy, M. Synthesis, stereochemistry and antimicrobial evaluation of t(3)-benzyl-r(2),c(6) -diarylpiperidin-4-one and its derivatives Eur. J. Med. Chem. 2007, 42, 593-605 (Pubitemid 46719484)
-
(2007)
European Journal of Medicinal Chemistry
, vol.42
, Issue.5
, pp. 593-605
-
-
Jayabharathi, J.1
Manimekalai, A.2
Consalata Vani, T.3
Padmavathy, M.4
-
16
-
-
0034676585
-
2,4-Disubstituted piperidines: Scaffolds for drug discovery
-
Watson, P. S.; Jiang, B.; Scott, B. 2,4-Disubstituted piperidines: Scaffolds for drug discovery Org. Lett. 2000, 2, 3679-3681
-
(2000)
Org. Lett.
, vol.2
, pp. 3679-3681
-
-
Watson, P.S.1
Jiang, B.2
Scott, B.3
-
17
-
-
0037459890
-
Recent advances in the synthesis of piperidones and piperidines
-
DOI 10.1016/S0040-4020(03)00295-3
-
Weintraub, P. M.; Sabol, J. S.; Kane, J. M.; Borcherding, D. R. Recent advances in the synthesis of piperidones and piperidines Tetrahedron 2003, 59, 2953-2989 (Pubitemid 36403778)
-
(2003)
Tetrahedron
, vol.59
, Issue.17
, pp. 2953-2989
-
-
Weintraub, P.M.1
Sabol, J.S.2
Kane, J.M.3
Borcherding, D.R.4
-
18
-
-
0035819644
-
Highly diastereoselective and enantioselective carbon-carbon bond formations in conjugate additions of lithiated N-Boc allylamines to nitroalkenes: Enantioselective synthesis of 3,4- and 3,4,5-substituted piperidines including (-)-paroxetine [15]
-
DOI 10.1021/ja005748w
-
Johnson, T. A.; Curtis, M. D.; Break, P. Highly diastereoselective and enantioselective carbon-carbon bond formations in conjugate additions of lithiated N-Boc allylamines to nitroalkenes: Enantioselective synthesis of 3,4- and 3,4,5-substituted piperidines including (-)-paroxetine J. Am. Chem. Soc. 2001, 123, 1004-1005 (Pubitemid 32151391)
-
(2001)
Journal of the American Chemical Society
, vol.123
, Issue.5
, pp. 1004-1005
-
-
Johnson, T.A.1
Curtis, M.D.2
Beak, P.3
-
19
-
-
38549126119
-
Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework
-
DOI 10.1016/j.bmc.2007.10.018, PII S096808960700884X
-
Kallstrom, S.; Leino, R. Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework Bioorg. Med. Chem. 2008, 16, 601-635 (Pubitemid 351163050)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.2
, pp. 601-635
-
-
Kallstrom, S.1
Leino, R.2
-
20
-
-
0036929215
-
New polyhydroxylated pyrrolidine, piperidine, and pyrrolizidine alkaloids from Scilla sibirica
-
DOI 10.1021/np020296h
-
Yamashita, T.; Yasuda, K.; Kizu, H.; Kameda, Y.; Watson, A. A.; Nash, R. J.; Fleet, G. W.; Asano, N. New polyhydroxylated pyrrolidine, piperidine, and pyrrolizidine alkaloids from Scilla sibirica J. Nat. Prod. 2002, 65, 1875-1881 (Pubitemid 36055440)
-
(2002)
Journal of Natural Products
, vol.65
, Issue.12
, pp. 1875-1881
-
-
Yamashita, T.1
Yasuda, K.2
Kizu, H.3
Kameda, Y.4
Watson, A.A.5
Nash, R.J.6
Fleet, G.W.J.7
Asano, N.8
-
21
-
-
9644295730
-
The discovery and preparation of disubstituted novel amino-aryl- piperidine- based renin inhibitors
-
DOI 10.1016/j.bmc.2004.09.056, PII S0968089604007734
-
Cody, W. L.; Holsworth, D. D.; Powell, N. A.; Jalaie, M.; Zhang, E.; Wang, W.; Samas, B.; Bryant, J.; Ostroski, R.; Ryan, M. J.; Edmunds, J. J. The discovery and preparation of disubstituted novel amino-aryl-piperidine-based renin inhibitors Bioorg. Med. Chem. 2005, 13, 59-68 (Pubitemid 39575692)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.1
, pp. 59-68
-
-
Cody, W.L.1
Holsworth, D.D.2
Powell, N.A.3
Jalaie, M.4
Zhang, E.5
Wang, W.6
Samas, B.7
Bryant, J.8
Ostroski, R.9
Ryan, M.J.10
Edmunds, J.J.11
-
22
-
-
0043234175
-
Discovery of (3S)-amino-(4R)-ethylpiperidinyl quinolones as potent antibacterial agents with a broad spectrum of activity and activity against resistant pathogens
-
DOI 10.1021/jm030272n
-
Hu, X. E.; Kim, N. K.; Gray, J. L.; Almstead, J.-I. K.; Seibel, W. L.; Ledoussal, B. Discovery of (3 S)-amino-(4 R)-ethylpiperidinyl quinolones as potent antibacterial agents with a broad spectrum of activity and activity against resistant pathogens J. Med. Chem. 2003, 46, 3655-3661 (Pubitemid 36988652)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.17
, pp. 3655-3661
-
-
Hu, X.E.1
Kim, N.K.2
Gray, J.L.3
Almstead, J.-I.K.4
Seibel, W.L.5
Ledoussal, B.6
-
23
-
-
2542633585
-
Synthesis, molecular modeling, and biological studies of novel piperidine-based analogues of cocaine: Evidence of unfavorable interactions proximal to the 3α-position of the piperidine ring
-
DOI 10.1021/jm0303296
-
Petukhov, P. A.; Zhang, J.; Wang, C. Z.; Ye, Y. P.; Johnson, K. M.; Kozikowski, A. P. Synthesis, molecular modeling, and biological studies of novel piperidine-based analogues of cocaine: Evidence of unfavorable interactions proximal to the 3α-position of the piperidine ring J. Med. Chem. 2004, 47, 3009-3018 (Pubitemid 38702698)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.12
, pp. 3009-3018
-
-
Petukhov, P.A.1
Zhang, J.2
Wang, C.Z.3
Ye, Y.P.4
Johnson, K.M.5
Kozikowski, A.P.6
-
24
-
-
12444334604
-
Discovery and structure-activity relationships of novel piperidine inhibitors of farnesyltransferase
-
DOI 10.1021/jm020522k
-
Nara, S.; Tanaka, R.; Eishima, J.; Hara, M.; Takahashi, Y.; Otaki, S.; Foglesong, R. J.; Hughes, P. F.; Shelley, T.; Kanda, Y. Discovery and structure-activity relationships of novel piperidine inhibitors of farnesyltransferase J. Med. Chem. 2003, 46, 2467-2473 (Pubitemid 36637930)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.12
, pp. 2467-2473
-
-
Nara, S.1
Tanaka, R.2
Eishima, J.3
Hara, M.4
Takahashi, Y.5
Otaki, S.6
Foglesong, R.J.7
Hughes, P.F.8
Turkington, S.9
Kanda, Y.10
-
25
-
-
33749149441
-
Design, synthesis, and antitumor activity of piperidone inhibitors of farnesyltransferase
-
Ge, Y. L.; Jiang, F. C. Design, synthesis, and antitumor activity of piperidone inhibitors of farnesyltransferase Acta Chim. Sin. A 2005, 63, 1613-1620
-
(2005)
Acta Chim. Sin. A
, vol.63
, pp. 1613-1620
-
-
Ge, Y.L.1
Jiang, F.C.2
-
26
-
-
33845944083
-
Design and synthesis of piperidine farnesyltransferase inhibitors with reduced glucuronidation potential
-
DOI 10.1016/j.bmc.2006.11.007, PII S0968089606009369
-
Tanaka, R.; Rubio, A.; Harn, N. K.; Gernert, D.; Grese, T. A.; Eishima, J.; Hara, M.; Yoda, N.; Ohashi, R.; Kuwabara, T.; Soga, S.; Akinaga, S.; Nara, S.; Kanda, Y. Design and synthesis of piperidine farnesyltransferase inhibitors with reduced glucuronidation potential Bioorg. Med. Chem. 2007, 15, 1363-1382 (Pubitemid 46038130)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.3
, pp. 1363-1382
-
-
Tanaka, R.1
Rubio, A.2
Harn, N.K.3
Gernert, D.4
Grese, T.A.5
Eishima, J.6
Hara, M.7
Yoda, N.8
Ohashi, R.9
Kuwabara, T.10
Soga, S.11
Akinaga, S.12
Nara, S.13
Kanda, Y.14
-
27
-
-
84862130926
-
Synthesis of polysubstituted 2-piperidinones via a Michael addition/nitro-Mannich/lactamization cascade
-
For a recent review, see
-
For a recent review, see: Liu, H.; Zhou, Z.; Sun, Q.; Li, Y.; Li, Y.; Liu, J.; Yan, P.; Wang, D.; Wang, C. Synthesis of polysubstituted 2-piperidinones via a Michael addition/nitro-Mannich/lactamization cascade ACS Comb. Sci. 2012, 14, 366-371
-
(2012)
ACS Comb. Sci.
, vol.14
, pp. 366-371
-
-
Liu, H.1
Zhou, Z.2
Sun, Q.3
Li, Y.4
Li, Y.5
Liu, J.6
Yan, P.7
Wang, D.8
Wang, C.9
-
28
-
-
18444378413
-
[3 + 3] Cycloadditions and related strategies in alkaloid natural product synthesis
-
DOI 10.1039/b502349c
-
Harrity, J. P. A.; Provoost, O. [3 + 3]-Cycloadditions and related strategies in alkaloid natural product synthesis Org. Biomol. Chem. 2005, 3, 1349-1358 (Pubitemid 40644159)
-
(2005)
Organic and Biomolecular Chemistry
, vol.3
, Issue.8
, pp. 1349-1358
-
-
Harrity, J.P.A.1
Provoost, O.2
-
30
-
-
22144459070
-
Diphenylprolinol silyl ethers as efficient organocatalysts for the asymmetric Michael reaction of aldehydes and nitroalkenes
-
DOI 10.1002/anie.200500599
-
Hayashi, Y.; Gotoh, H.; Hayashi, T.; Shoji, M. Diphenylprolinol silyl ethers as efficient organocatalysts for the asymmetric Michael reaction of aldehydes and nitroalkenes Angew. Chem., Int. Ed. 2005, 44, 4212-4215 (Pubitemid 40968498)
-
(2005)
Angewandte Chemie - International Edition
, vol.44
, Issue.27
, pp. 4212-4215
-
-
Hayashi, Y.1
Gotoh, H.2
Hayashi, T.3
Shoji, M.4
-
31
-
-
13444267885
-
Enantioselective organocatalyzed α sulfenylation of aldehydes
-
Marigo, M.; Wabnitz, T. C.; Fielenbach, D.; Jorgensen, K. A. Enantioselective organocatalyzed α sulfenylation of aldehydes Angew. Chem., Int. Ed. 2005, 44, 794-797
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 794-797
-
-
Marigo, M.1
Wabnitz, T.C.2
Fielenbach, D.3
Jorgensen, K.A.4
-
32
-
-
20444441594
-
Enantioselective formation of stereogenic carbon - Fluorine centers by a simple catalytic method
-
DOI 10.1002/anie.200500395
-
Marigo, M.; Fielenbach, D.; Braunton, A.; Kjasgaard, A.; Jorgensen, K. A. Enantioselective formation of stereogenic carbon-fluorine centers by a simple catalytic method Angew. Chem., Int. Ed. 2005, 44, 3703-3706 (Pubitemid 40817183)
-
(2005)
Angewandte Chemie - International Edition
, vol.44
, Issue.24
, pp. 3703-3706
-
-
Marigo, M.1
Fielenbach, D.2
Braunton, A.3
Kjaersgaard, A.4
Jorgensen, K.A.5
-
33
-
-
51749084445
-
α,α-Diarylprolinol ethers: New tools for functionalization of carbonyl compounds
-
Mielgo, A.; Palomo, C. α,α-Diarylprolinol ethers: New tools for functionalization of carbonyl compounds Chem.-Asian J. 2008, 3, 922-948
-
(2008)
Chem.-Asian J.
, vol.3
, pp. 922-948
-
-
Mielgo, A.1
Palomo, C.2
-
34
-
-
47049097671
-
Diphenylprolinol silyl ether as a catalyst in an enantioselective, catalytic, formal aza [3 + 3] cycloaddition reaction for the formation of enantioenriched piperidines
-
Hayashi, Y.; Gotoh, H.; Masui, R.; Shikawa, H. Diphenylprolinol silyl ether as a catalyst in an enantioselective, catalytic, formal aza [3 + 3] cycloaddition reaction for the formation of enantioenriched piperidines Angew. Chem., Int. Ed. 2008, 47, 4012-4015
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 4012-4015
-
-
Hayashi, Y.1
Gotoh, H.2
Masui, R.3
Shikawa, H.4
-
35
-
-
34250195722
-
Enantioselective synthesis of 3,3-disubstituted piperidine derivatives by enolate dialkylation of phenylglycinol-derived oxazolopiperidone lactams
-
DOI 10.1021/jo070397q
-
Amat, M.; Lozano, O.; Escolano, C.; Molins, E.; Bosch, J. Enantioselective synthesis of 3,3-disubstituted piperidine derivatives by enolate dialkylation of phenylglycinol-derived oxazolopiperidone lactams J. Org. Chem. 2007, 72, 4431-4439 (Pubitemid 46903314)
-
(2007)
Journal of Organic Chemistry
, vol.72
, Issue.12
, pp. 4431-4439
-
-
Amat, M.1
Lozano, O.2
Escolano, C.3
Molins, E.4
Bosch, J.5
-
36
-
-
0037424287
-
-
Amat, M.; Llor, N.; Hidalgo, J.; Escolano, C.; Bosch, J. J. Org. Chem. 2003, 68, 1919-1928
-
(2003)
J. Org. Chem.
, vol.68
, pp. 1919-1928
-
-
Amat, M.1
Llor, N.2
Hidalgo, J.3
Escolano, C.4
Bosch, J.5
-
37
-
-
70350173755
-
An unexpected oxidation in the generation of cyclopenta[ c ]piperidines by ring-closing metathesis
-
Amat, M.; Brunaccini, E.; Checa, B. A.; Perez, M.; Llor, N. R.; Bosch, J. An unexpected oxidation in the generation of cyclopenta[ c ]piperidines by ring-closing metathesis Org. Lett. 2009, 11, 4370-4373
-
(2009)
Org. Lett.
, vol.11
, pp. 4370-4373
-
-
Amat, M.1
Brunaccini, E.2
Checa, B.A.3
Perez, M.4
Llor, N.R.5
Bosch, J.6
-
38
-
-
73949084123
-
Total synthesis of (-)-lycoperine A
-
Nakamura, Y.; Burke, A. M.; Kotani, S.; Ziller, J. W.; Rychnovsky, S. D. Total synthesis of (-)-lycoperine A Org. Lett. 2009, 12, 72-75
-
(2009)
Org. Lett.
, vol.12
, pp. 72-75
-
-
Nakamura, Y.1
Burke, A.M.2
Kotani, S.3
Ziller, J.W.4
Rychnovsky, S.D.5
-
39
-
-
76049120038
-
A short synthesis of indolizidine (+)-209B from (3 R,6 S,8A S)-(-)-6-methyl-3-phenyl-hexahydro-oxazolo[3,2- A ]pyridin-5-one
-
Gnecco, D.; Lumbreras, A. M.; Teran, J. L.; Galindo, A.; Juarez, J. R.; Orea, M. L.; Castro, A.; Enriquez, R. G.; Reynolds, W. F. A short synthesis of indolizidine (+)-209B from (3 R,6 S,8A S)-(-)-6-methyl-3-phenyl-hexahydro- oxazolo[3,2- a ]pyridin-5-one Heterocycles 2009, 78, 2589-2592
-
(2009)
Heterocycles
, vol.78
, pp. 2589-2592
-
-
Gnecco, D.1
Lumbreras, A.M.2
Teran, J.L.3
Galindo, A.4
Juarez, J.R.5
Orea, M.L.6
Castro, A.7
Enriquez, R.G.8
Reynolds, W.F.9
-
40
-
-
84862169693
-
Regio- and stereoselective syntheses of piperidine derivatives via ruthenium-catalyzed coupling of propargylic amides and allylic alcohols
-
Murugesan, S.; Jiang, F.; Achard, M.; Bruneau, C.; De′rien, S. Regio- and stereoselective syntheses of piperidine derivatives via ruthenium-catalyzed coupling of propargylic amides and allylic alcohols Chem. Commun. 2012, 48, 6589-6591
-
(2012)
Chem. Commun.
, vol.48
, pp. 6589-6591
-
-
Murugesan, S.1
Jiang, F.2
Achard, M.3
Bruneau, C.4
Derien, S.5
-
41
-
-
77954290900
-
Highly flexible synthesis of chiral azacycles via iridium-catalyzed hydrogenation
-
Verendel, J. J.; Zhou, T. G.; Li, J. Q.; Paptchikhine, A.; Lebedev, O.; Andersson, P. G. Highly flexible synthesis of chiral azacycles via iridium-catalyzed hydrogenation J. Am. Chem. Soc. 2010, 132, 8880-8881
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8880-8881
-
-
Verendel, J.J.1
Zhou, T.G.2
Li, J.Q.3
Paptchikhine, A.4
Lebedev, O.5
Andersson, P.G.6
-
42
-
-
79961033802
-
Synthesis of enantiopure substituted piperidines via an aziridinium ring expansion
-
Jarvis, S. B. D.; Charette, A. B. Synthesis of enantiopure substituted piperidines via an aziridinium ring expansion Org. Lett. 2011, 13, 3830-3833
-
(2011)
Org. Lett.
, vol.13
, pp. 3830-3833
-
-
Jarvis, S.B.D.1
Charette, A.B.2
-
43
-
-
77957824693
-
Enantio- and diastereoselective synthesis of piperidines by coupling of four components in a "one-pot" sequence involving diphenylprolinol silyl ether mediated michael reaction
-
Urushima, T.; Sakamoto, D.; Ishikawa, H.; Hayashi, Y. Enantio- and diastereoselective synthesis of piperidines by coupling of four components in a "one-pot" sequence involving diphenylprolinol silyl ether mediated michael reaction Org. Lett. 2010, 12, 4588-4591
-
(2010)
Org. Lett.
, vol.12
, pp. 4588-4591
-
-
Urushima, T.1
Sakamoto, D.2
Ishikawa, H.3
Hayashi, Y.4
-
44
-
-
84855960229
-
Synthesis of stereodefined 3,4-disubstituted piperidines through rearrangement of 2-(2-bromo-1,1-dimethylethyl)azetidines
-
Mollet, K.; Broeckx, L.; D'hoogue, M.; De Kimpe, N. Synthesis of stereodefined 3,4-disubstituted piperidines through rearrangement of 2-(2-bromo-1,1-dimethylethyl)azetidines Heterocycles 2011, 84, 431-447
-
(2011)
Heterocycles
, vol.84
, pp. 431-447
-
-
Mollet, K.1
Broeckx, L.2
D'Hoogue, M.3
De Kimpe, N.4
-
45
-
-
80054122796
-
Stereoselective synthesis of cis-3,4-disubstituted piperidines through ring transformation of 2-(2-mesyloxyethyl)azetidines
-
Mollet, K.; Catak, S.; Waroquier, M.; Van Speybroeck, V.; D'hoogue, M.; De Kimpe, N. Stereoselective synthesis of cis-3,4-disubstituted piperidines through ring transformation of 2-(2-mesyloxyethyl)azetidines J. Org. Chem. 2011, 76, 8364-8375
-
(2011)
J. Org. Chem.
, vol.76
, pp. 8364-8375
-
-
Mollet, K.1
Catak, S.2
Waroquier, M.3
Van Speybroeck, V.4
D'Hoogue, M.5
De Kimpe, N.6
-
46
-
-
33646452114
-
Ring transformation of 2-(haloalkyl)azetidines into 3,4-disubstituted pyrrolidines and piperidines
-
DOI 10.1021/ol0530676
-
Van Brabandt, W.; Van Landeghem, R.; De Kimpe, N. Ring transformation of 2-(haloalkyl)azetidines into 3,4-disubstituted pyrrolidines and piperidines Org. Lett. 2006, 8, 1105-1108 (Pubitemid 43690671)
-
(2006)
Organic Letters
, vol.8
, Issue.6
, pp. 1105-1108
-
-
Van Brabandt, W.1
Van Landeghem, R.2
De Kimpe, N.3
-
47
-
-
0141741220
-
Hetero [6+3] cycloaddition of fulvenes with N-alkylidene glycine esters: A facile synthesis of the delavayine and incarvillateine framework
-
DOI 10.1021/ol034329b
-
Hong, B.-C.; Gupta, A. K.; Wu, M.-F.; Liao, J.-H.; Lee, G.-H. Hetero [6 + 3] cycloaddition of fulvenes with N-alkylidene glycine esters: A facile synthesis of the delavayine and incarvillateine framework Org. Lett. 2003, 5, 1689-1692 (Pubitemid 37162005)
-
(2003)
Organic Letters
, vol.5
, Issue.10
, pp. 1689-1692
-
-
Hong, B.-C.1
Gupta, A.K.2
Wu, M.-F.3
Liao, J.-H.4
Lee, G.-H.5
-
48
-
-
84874591056
-
Fulvenes as effective dipolarophiles in copper(I)-catalyzed [6 + 3] cycloaddition of azomethine ylides: Asymmetric construction of piperidine derivatives
-
He, Z.-L.; Teng, H.-L.; Wang, C.-J. Fulvenes as effective dipolarophiles in copper(I)-catalyzed [6 + 3] cycloaddition of azomethine ylides: Asymmetric construction of piperidine derivatives Angew. Chem., Int. Ed. 2013, 52, 2934-2938
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 2934-2938
-
-
He, Z.-L.1
Teng, H.-L.2
Wang, C.-J.3
-
49
-
-
84872196538
-
Efficient and chemoselective reduction of pyridines to tetrahydropyridines and piperidine via rhodium-catalyzed transfer hydrogenation
-
Wu, J.; Tang, W.; Pettman, A.; Xiao, J. Efficient and chemoselective reduction of pyridines to tetrahydropyridines and piperidine via rhodium-catalyzed transfer hydrogenation Adv. Synth. Catal. 2013, 355, 35-40
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 35-40
-
-
Wu, J.1
Tang, W.2
Pettman, A.3
Xiao, J.4
-
50
-
-
84872697729
-
Organocatalytic asymmetric multicomponent reactions of aromatic aldehydes and anilines with β-ketoesters: Facile and atom-economical access to chiral tetrahydropyridines
-
Li, X.; Zhao, Y.; Qu, H.; Mao, Z.; Lin, X. Organocatalytic asymmetric multicomponent reactions of aromatic aldehydes and anilines with β-ketoesters: facile and atom-economical access to chiral tetrahydropyridines Chem. Commun. 2013, 49, 1401-1403
-
(2013)
Chem. Commun.
, vol.49
, pp. 1401-1403
-
-
Li, X.1
Zhao, Y.2
Qu, H.3
Mao, Z.4
Lin, X.5
-
51
-
-
84865800821
-
Zinc hydrogen sulfate promoted multi-component preparation of highly functionalized piperidines
-
Ghashang, M. Zinc hydrogen sulfate promoted multi-component preparation of highly functionalized piperidines Lett. Org. Chem. 2012, 9, 497-502
-
(2012)
Lett. Org. Chem.
, vol.9
, pp. 497-502
-
-
Ghashang, M.1
-
52
-
-
84864608678
-
Nickel(II) chloride hexahydrate as an efficient catalyst for the preparation of highly functionalized piperidine derivatives
-
Shafiee, M. R. M.; Najafabadi, B. H.; Ghashang, M. Nickel(II) chloride hexahydrate as an efficient catalyst for the preparation of highly functionalized piperidine derivatives J. Chem. Res. 2012, 36, 336-339
-
(2012)
J. Chem. Res.
, vol.36
, pp. 336-339
-
-
Shafiee, M.R.M.1
Najafabadi, B.H.2
Ghashang, M.3
-
53
-
-
34250850717
-
Pot, atom and step economic (PASE) synthesis of highly functionalized piperidines: A five-component condensation
-
DOI 10.1016/j.tetlet.2007.05.141, PII S0040403907010374
-
Clarke, P. A.; Zaytzev, A. V.; Whitwood, A. C. Pot, atom and step economic (PASE) synthesis of highly functionalized piperidines: A five-component condensation Tetrahedron Lett. 2007, 48, 5209-5212 (Pubitemid 46977005)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.30
, pp. 5209-5212
-
-
Clarke, P.A.1
Zaytzev, A.V.2
Whitwood, A.C.3
-
54
-
-
84860179135
-
NHC-catalysed diastereoselective synthesis of multifunctionalised piperidines via cascade reaction of enals with azalactones
-
Singh, A. K.; Chawla, R.; Rai, A.; Yadav, L. D. S. NHC-catalysed diastereoselective synthesis of multifunctionalised piperidines via cascade reaction of enals with azalactones Chem. Commun. 2012, 48, 3766-3768
-
(2012)
Chem. Commun.
, vol.48
, pp. 3766-3768
-
-
Singh, A.K.1
Chawla, R.2
Rai, A.3
Yadav, L.D.S.4
-
55
-
-
80053989120
-
Design, synthesis and biological evaluation of optically pure functionalized spiro[5,5] undecane-1,5,9-triones as HIV-1 inhibitors
-
Ramachary, D. B.; Reddy, Y. V.; Banerjee, A.; Banerjee, S. Design, synthesis and biological evaluation of optically pure functionalized spiro[5,5] undecane-1,5,9-triones as HIV-1 inhibitors Org. Biomol. Chem. 2011, 9, 7282-7286
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 7282-7286
-
-
Ramachary, D.B.1
Reddy, Y.V.2
Banerjee, A.3
Banerjee, S.4
-
56
-
-
53249096085
-
Total structure and biological properties of laxaphycins A and B, cyclic lipopeptides from the marine cyanobacterium Lyngbya majuscula
-
Bonnard, I.; Rolland, M.; Francisco, C.; Banaigs, B. Synthesis and biological properties of laxaphycins A and B, cyclic lipopeptides from the marine cyanobacterium Lyngbya Lett. Pept. Sci. 1997, 4, 289-292 (Pubitemid 127505462)
-
(1997)
Letters in Peptide Science
, vol.4
, Issue.4-6
, pp. 289-292
-
-
Bonnard, I.1
Rolland, M.2
Francisco, C.3
Banaigs, B.4
-
57
-
-
26444591495
-
Michael addition approach for the synthesis of novel spiro compounds and 2-substituted malonic acid derivatives from Meldrum's acid
-
DOI 10.1016/j.tetlet.2005.09.030, PII S0040403905019854
-
Chande, S. M.; Khanwelkar, R. R. Michael addition approach for the synthesis of novel spiro compounds and 2-substituted malonic acid derivatives from Meldrum's acid Tetrahedron Lett. 2005, 46, 7787-7792 (Pubitemid 41425731)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.45
, pp. 7787-7792
-
-
Chande, M.S.1
Khanwelkar, R.R.2
-
58
-
-
41149101973
-
Meldrum's acid and related compounds in the synthesis of natural products and analogs
-
Ivanov, A. S. Meldrum's acid and related compounds in the synthesis of natural products and analogs Chem. Soc. Rev. 2008, 37, 789-811
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 789-811
-
-
Ivanov, A.S.1
-
59
-
-
33846959848
-
Synthesis and HIV-1 integrase inhibitory activity of spiroundecane(ene) derivatives
-
DOI 10.1016/j.bmcl.2006.11.094, PII S0960894X06013837
-
Shults, E. E.; Semenova, E. A.; Johnson, A. A.; Bondarenko, S. P.; Bagryanskaya, I. Y.; Gatilov, Y. V.; Tolstikov, G. A.; Pommier, Y. Synthesis and HIV-1 integrase inhibitory activity of spiroundecane(ene) derivatives Bioorg. Med. Chem. Lett. 2007, 17, 1362-1368 (Pubitemid 46242192)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.5
, pp. 1362-1368
-
-
Shults, E.E.1
Semenova, E.A.2
Johnson, A.A.3
Bondarenko, S.P.4
Bagryanskaya, I.Y.5
Gatilov, Y.V.6
Tolstikov, G.A.7
Pommier, Y.8
-
60
-
-
0842283435
-
Synthesis of carbazoles by a balanced four component condensation
-
Cochard, F.; Laronze, M.; Sigaut, P.; Sapi, J.; Laronze, J. Y. Synthesis of carbazoles by a balanced four component condensation Tetrahedron Lett. 2004, 45, 1703-1705
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 1703-1705
-
-
Cochard, F.1
Laronze, M.2
Sigaut, P.3
Sapi, J.4
Laronze, J.Y.5
-
61
-
-
77955220034
-
New multicomponent domino reactions (MDRs) in water: Highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4- b ]pyridines
-
Ma, N.; Jiang, B.; Zhang, G.; Tu, S.-J.; Wever, W.; Li, G. New multicomponent domino reactions (MDRs) in water: Highly chemo-, regio- and stereoselective synthesis of spiro{[1,3]dioxanopyridine}-4,6-diones and pyrazolo[3,4- b ]pyridines Green Chem. 2010, 12, 1357-1361
-
(2010)
Green Chem.
, vol.12
, pp. 1357-1361
-
-
Ma, N.1
Jiang, B.2
Zhang, G.3
Tu, S.-J.4
Wever, W.5
Li, G.6
-
62
-
-
84864720617
-
Novel Synthesis of trans-4,6-diaryl-5-nitropiperidin-2-ones via four-component reaction from substituted nitrostyrenes, aromatic aldehydes, dimethyl malonate, and formamide
-
Zhou, Z.; Liu, H.; Sun, Q.; Li, Y.; Yang, J.; Liu, J.; Yan, P.; Wang, C. Novel Synthesis of trans-4,6-diaryl-5-nitropiperidin-2-ones via four-component reaction from substituted nitrostyrenes, aromatic aldehydes, dimethyl malonate, and formamide Synlett 2012, 2255-2260
-
(2012)
Synlett
, pp. 2255-2260
-
-
Zhou, Z.1
Liu, H.2
Sun, Q.3
Li, Y.4
Yang, J.5
Liu, J.6
Yan, P.7
Wang, C.8
-
63
-
-
84896803117
-
-
Int. Patent WO2001077100.
-
Arnold, E. P.; Chappie, T. A.; Huang, J.; Humphery, J. M.; Nagel, A. A.; O'Neill, B. T. Synthesis of benzoamide piperidine containing compounds as substance P antagonists. Int. Patent WO2001077100, 2001.
-
(2001)
Synthesis of Benzoamide Piperidine Containing Compounds As Substance P Antagonists
-
-
Arnold, E.P.1
Chappie, T.A.2
Huang, J.3
Humphery, J.M.4
Nagel, A.A.5
O'Neill, B.T.6
-
64
-
-
67249092537
-
Diastereoselective synthesis of 2,3,6-trisubstituted piperidines
-
Humphery, J. M.; Arnold, E. P.; Chappie, T. A.; Feltenberger, J. B.; Nagel, A. A.; Simon, W.; Suarez-Contreras, M.; Tom, N. J.; O'Neill, B. T. Diastereoselective synthesis of 2,3,6-trisubstituted piperidines J. Org. Chem. 2009, 74 (12) 4525-4536
-
(2009)
J. Org. Chem.
, vol.74
, Issue.12
, pp. 4525-4536
-
-
Humphery, J.M.1
Arnold, E.P.2
Chappie, T.A.3
Feltenberger, J.B.4
Nagel, A.A.5
Simon, W.6
Suarez-Contreras, M.7
Tom, N.J.8
O'Neill, B.T.9
-
66
-
-
0027437887
-
3H]-cis-3-[(2-methoxybenzyl)amino]-2-phenylpiperidine, a highly potent and selective nonpeptide substance P receptor antagonist radioligand
-
DOI 10.1021/jm00073a022
-
Rosen, T.; Seeger, T. F.; McLean, S.; Desai, M. C.; Guarino, K. J.; Bryce, D.; Pratt, K.; Heym, J.; Chalabi, P. M.; Windels, J. H. Synthesis, in vitro binding profile, and autoradiographic analysis of [3 H ]- cis -3-[(2-methoxybenzyl)amino]-2-phenyl piperidine, A highly potent and selective nonpeptide substance P receptor antagonist radioligand J. Med. Chem. 1993, 36 (21) 3197-3201 (Pubitemid 23326276)
-
(1993)
Journal of Medicinal Chemistry
, vol.36
, Issue.21
, pp. 3197-3201
-
-
Rosen, T.1
Seeger, T.F.2
McLean, S.3
Desai, M.C.4
Guarino, K.J.5
Bryce, D.6
Pratt, K.7
Heym, J.8
Chalabi, P.M.9
Windels, J.H.10
Roth, R.W.11
|