-
1
-
-
18144369212
-
β-Lactams: Synthesis, stereochemistry, synthons and biological evaluation
-
Banik BK: β-Lactams: Synthesis, stereochemistry, synthons and biological evaluation. Curr Med Chem (2004) 11(14): 1813-1964.
-
(2004)
Curr Med Chem
, vol.11
, Issue.14
, pp. 1813-1964
-
-
Banik, B.K.1
-
2
-
-
78149332413
-
Novel anticancer β-lactams
-
Hetereocyclic Scaffolds I. Banik BK (Ed) Springer-Verlag, Berlin-Heidelberg, Germany
-
Banik BK, Banik I, Becker FF: Novel anticancer β-lactams. In: Topics in Heterocyclic Chemistry, Vol 22. Hetereocyclic Scaffolds I. Banik BK (Ed), Springer-Verlag, Berlin-Heidelberg, Germany (2010):349-374.
-
(2010)
Topics in Heterocyclic Chemistry
, vol.22
, pp. 349-374
-
-
Banik, B.K.1
Banik, I.2
Becker, F.F.3
-
3
-
-
36849034419
-
β-Lactams: Versatile building blocks for the stereoselective synthesis of non-β-lactam products
-
Alcaide B, Almendros P, Aragoncillo C: β-Lactams: Versatile building blocks for the stereoselective synthesis of non-β-lactam products. Chem Rev (2007) 107(11):4437-4492.
-
(2007)
Chem Rev
, vol.107
, Issue.11
, pp. 4437-4492
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
-
4
-
-
72049122384
-
Azetidines: New tools for the synthesis of nitrogen heterocycles
-
Couty F, Gwilherm E: Azetidines: New tools for the synthesis of nitrogen heterocycles. Synlett (2009) (19):3053-3064.
-
(2009)
Synlett
, vol.19
, pp. 3053-3064
-
-
Couty, F.1
Gwilherm, E.2
-
6
-
-
53049101572
-
Preparation of β-lactams by [2+2] cycloaddition of ketenes and imines
-
Fu N, Tidwell TT: Preparation of β-lactams by [2+2] cycloaddition of ketenes and imines. Tetrahedron (2008) 64(46):10465-10496.
-
(2008)
Tetrahedron
, vol.64
, Issue.46
, pp. 10465-10496
-
-
Fu, N.1
Tidwell, T.T.2
-
7
-
-
38849098435
-
Hugo (Ugo) Schiff Schiff bases and a century of β-lactam synthesis
-
Tidwell, TT: Hugo (Ugo) Schiff, Schiff bases, and a century of β-lactam synthesis. Angew Chem Int Ed (2008) 47(6): 1016-1020.
-
(2008)
Angew Chem Int Ed
, vol.47
, Issue.6
, pp. 1016-1020
-
-
Tidwell, T.T.1
-
8
-
-
51649103509
-
The mechanism of the ketene-imine (Staudinger) reaction in its centennial: Still an unsolved problem
-
Cossio FP, Arrieta A, Sierra MA: The mechanism of the ketene-imine (Staudinger) reaction in its centennial: Still an unsolved problem Acc Chem Res (2008) 41(8):925-936.
-
(2008)
Acc Chem Res
, vol.41
, Issue.8
, pp. 925-936
-
-
Cossio, F.P.1
Arrieta, A.2
Sierra, M.A.3
-
9
-
-
53049085693
-
Stereoselectivity in the synthesis of 2-azetidinones from ketenes and imines via the Staudinger reaction
-
Xu J: Stereoselectivity in the synthesis of 2-azetidinones from ketenes and imines via the Staudinger reaction. ARKIVOC (2009) (ix):21-44.
-
(2009)
ARKIVOC
, vol.10
, pp. 21-44
-
-
Xu, J.1
-
10
-
-
33845183324
-
The ester-imine condensation route to β-lactams
-
Hart DJ, Ha DC: The ester-imine condensation route to β-lactams. Chem Rev (1989) 89(7):1447-1465.
-
(1989)
Chem Rev
, vol.89
, Issue.7
, pp. 1447-1465
-
-
Hart, D.J.1
Ha, D.C.2
-
11
-
-
55249112288
-
Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines
-
Gianelli C, Sambri L, Carlone A, Bartoli G, Melchiorre P: Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines. Angew Chem Int Ed (2008) 47(45):8700-8702.
-
(2008)
Angew Chem Int Ed
, vol.47
, Issue.45
, pp. 8700-8702
-
-
Gianelli, C.1
Sambri, L.2
Carlone, A.3
Bartoli, G.4
Melchiorre, P.5
-
12
-
-
34948844484
-
Synthesis of β-lactams using the Kinugasa reaction
-
Runa P, Ghosh SC, Chandra K, Basak A: Synthesis of β-lactams using the Kinugasa reaction. Synlett (2007) (15):2321-2330.
-
(2007)
Synlett
, vol.15
, pp. 2321-2330
-
-
Runa, P.1
Ghosh, S.C.2
Chandra, K.3
Basak, A.4
-
13
-
-
58049196954
-
Rapid synthesis of 1, 3, 4,4-tetrasubstituted β-lactams from methyleneaziridines using a four-component reaction
-
Cariou CCA, Clarkson GJ, Shipman M: Rapid synthesis of 1,3,4,4-tetrasubstituted β-lactams from methyleneaziridines using a four-component reaction. J Org Chem (2008) 73(24):9762-9764.
-
(2008)
J Org Chem
, vol.73
, Issue.24
, pp. 9762-9764
-
-
Cca, C.1
Clarkson, G.J.2
Shipman, M.3
-
14
-
-
4143125756
-
Advances in the catalytic asymmetric synthesis of β-lactams
-
France S, Weatherwax A, Taggi AE, Lectka T: Advances in the catalytic asymmetric synthesis of β-lactams. Acc Chem Res (2004) 37(8):592-600.
-
(2004)
Acc Chem Res
, vol.37
, Issue.8
, pp. 592-600
-
-
France, S.1
Weatherwax, A.2
Taggi, A.E.3
Lectka, T.4
-
15
-
-
24044436551
-
Catalytic asymmetric Staudinger reactions to form β-lactams: An unanticipated dependence of diastereoselectivity on the choice of the nitrogen substituent
-
Lee EC, Hodous BL, Bergin E, Shih C, Fu GC: Catalytic asymmetric Staudinger reactions to form β-lactams: An unanticipated dependence of diastereoselectivity on the choice of the nitrogen substituent. J Am Chem Soc (2005) 127(33):11586-11587.
-
(2005)
J Am Chem Soc
, vol.127
, Issue.33
, pp. 11586-11587
-
-
Lee, E.C.1
Hodous, B.L.2
Bergin, E.3
Shih, C.4
Fu, G.C.5
-
16
-
-
38749111840
-
Chiral N-heterocyclic carbene catalyzed Staudinger reaction of ketenes with imines: Highly enantioselective synthesis of N-Boc β-lactams
-
Zhand YR, He L, Wu X, Shao PL, Ye S: Chiral N-heterocyclic carbene catalyzed Staudinger reaction of ketenes with imines: Highly enantioselective synthesis of N-Boc β-lactams. Org Lett (2008) 10(2):277-280.
-
(2008)
Org Lett
, vol.10
, Issue.2
, pp. 277-280
-
-
Zhand, Y.R.1
He, L.2
Wu, X.3
Shao, P.L.4
Ye, S.5
-
17
-
-
70949088924
-
β-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoglycerol lipase
-
Feledziak M, Michaux C, Urbach A, Labar G, Muccioli GG, Lambert DM, Marchand-Brynaert J: β-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoglycerol lipase. J Med Chem (2009) 52(22):7054-7068.
-
(2009)
J Med Chem
, vol.52
, Issue.22
, pp. 7054-7068
-
-
Feledziak, M.1
Michaux, C.2
Urbach, A.3
Labar, G.4
Muccioli, G.G.5
Lambert, D.M.6
Marchand-Brynaert, J.7
-
18
-
-
52649161380
-
Click saccharide/ β-lactam hybrids for lectin inhibition
-
Palomo C, Aizpurua JM, Balentová E, Azcune I, Santos JI, Jiménez-Barbero J, Cañada J, Miranda JI: "Click" saccharide/ β-lactam hybrids for lectin inhibition. Org Lett (2008) 10(11): 2227-2230.
-
(2008)
Org Lett
, vol.10
, Issue.11
, pp. 2227-2230
-
-
Palomo, C.1
Aizpurua, J.M.2
Balentová, E.3
Azcune, I.4
Santos, J.I.5
Jiménez-Barbero, J.6
Cañada, J.7
Miranda, J.I.8
-
19
-
-
53749087548
-
Synthesis of the mannopeptimycin disaccharide and its conjugation with 4-alkylidene-β-lactams
-
Adinolf M, Giacomini D, Iadonisi A, Quintavalla A, Valerio S: Synthesis of the mannopeptimycin disaccharide and its conjugation with 4-alkylidene-β-lactams. Eur J Org Chem (2008) (17):2895-2899.
-
(2008)
Eur J Org Chem
, vol.17
, pp. 2895-2899
-
-
Adinolf, M.1
Giacomini, D.2
Iadonisi, A.3
Quintavalla, A.4
Valerio, S.5
-
20
-
-
77957888641
-
Novel aspects on the preparation of spirocyclic and fused unsual β-lactams
-
Hetereocyclic Scaffolds I. Banik BK (Ed) Springer-Verlag, Berlin-Heidelberg, Germany
-
Alcaide B, Almendros P: Novel aspects on the preparation of spirocyclic and fused unsual β-lactams. In: Topics in Heterocyclic Chemistry, Vol 22. Hetereocyclic Scaffolds I. Banik BK (Ed), Springer-Verlag, Berlin-Heidelberg, Germany (2010):1-48.
-
(2010)
Topics in Heterocyclic Chemistry
, vol.22
, pp. 1-48
-
-
Alcaide, B.1
Almendros, P.2
-
21
-
-
3042673283
-
Strategies for the stereocontrolled formation of oxygen analogues of penicillins and cephalosporins
-
Lysek R, Borsuk K, Furman B, Kałuza Z, Kazimierski A, Chmielewski M: Strategies for the stereocontrolled formation of oxygen analogues of penicillins and cephalosporins. Curr Med Chem (2004) 11(14):1813-1835.
-
(2004)
Curr Med Chem
, vol.11
, Issue.14
, pp. 1813-1835
-
-
Lysek, R.1
Borsuk, K.2
Furman, B.3
Kałuza, Z.4
Kazimierski, A.5
Chmielewski, M.6
-
22
-
-
58649113013
-
An enantioselective synthesis of 3,4-benzo-5-oxacephams
-
Kozioł A, Frelek J, Wonica M, Furman B, Chmielewski M: An enantioselective synthesis of 3,4-benzo-5-oxacephams. Eur J Org Chem (2009) (3):338-341.
-
(2009)
Eur J Org Chem
, vol.3
, pp. 338-341
-
-
Kozioł, A.1
Frelek, J.2
Wonica, M.3
Furman, B.4
Chmielewski, M.5
-
23
-
-
14844365696
-
Streptogramins, oxazolidinones, and other inhibitors of bacterial protein synthesis
-
Mukhtar TA, Wright GD: Streptogramins, oxazolidinones, and other inhibitors of bacterial protein synthesis. Chem Rev (2005) 105(2):529-542.
-
(2005)
Chem Rev
, vol.105
, Issue.2
, pp. 529-542
-
-
Mukhtar, T.A.1
Wright, G.D.2
-
24
-
-
0034704737
-
2 ligand for peptidomimetic-based HIV protease inhibitors
-
2 ligand for peptidomimetic-based HIV protease inhibitors. J Med Chem (2000) 43(6):1094-1108.
-
(2000)
J Med Chem
, vol.43
, Issue.6
, pp. 1094-1108
-
-
Beaulieu, P.L.1
Anderson, P.C.2
Cameron, D.R.3
Croteasu, G.4
Gorys, V.5
Grand-Maître, C.6
Lamarre, D.7
Liard, F.8
Paris, W.9
Plamondon, L.10
Soucy, F.11
-
25
-
-
39349107529
-
Synthesis of novel enantiopure 4-hydroxypipecolic acid derivatives with a bicyclic β-lactam structure from a common 3-azido-4-oxoazetidine-2- carbaldehyde precursor
-
Alcaide B, Almendros P, Luna A, Martínez del Campo T: Synthesis of novel enantiopure 4-hydroxypipecolic acid derivatives with a bicyclic β-lactam structure from a common 3-azido-4-oxoazetidine-2-carbaldehyde precursor. J Org Chem (2008) 73(4):1635-1638.
-
(2008)
J Org Chem
, vol.73
, Issue.4
, pp. 1635-1638
-
-
Alcaide, B.1
Almendros, P.2
Luna, A.3
Martínez Del Campo, T.4
-
26
-
-
62549090567
-
Large ring 1,3-bridged 2-azetidinones: Experimental and theoretical studies
-
Urbach A, Dive G, Tinant B, Duval V, Marchand-Brynaert J: Large ring 1,3-bridged 2-azetidinones: Experimental and theoretical studies. Eur J Med Chem (2009) 44(5):2071-2080.
-
(2009)
Eur J Med Chem
, vol.44
, Issue.5
, pp. 2071-2080
-
-
Urbach, A.1
Dive, G.2
Tinant, B.3
Duval, V.4
Marchand-Brynaert, J.5
-
27
-
-
63849228551
-
Novel large-ring 1,3-bridged 2-azetidinones as potential inhibitors of penicillin-binding proteins
-
Urbach A, Dive G, Marchand-Brynaert J: Novel large-ring 1,3-bridged 2-azetidinones as potential inhibitors of penicillin-binding proteins. Eur J Org Chem (2009) (11): 1757-1770.
-
(2009)
Eur J Org Chem
, vol.11
, pp. 1757-1770
-
-
Urbach, A.1
Dive, G.2
Marchand-Brynaert, J.3
-
28
-
-
0023611698
-
Marine alkaloids. 12. Chartellines, halogenated β-lactam alkaloids from the marine bryozoan Chartella papyracea
-
Anthoni U, Chevolot L, Larsen C, Nielsen PH, Christophersen C: Marine alkaloids. 12. Chartellines, halogenated β-lactam alkaloids from the marine bryozan Chartella papyracea. J Org Chem (1987) 52(21):4709-4712. (Pubitemid 18052645)
-
(1987)
Journal of Organic Chemistry
, vol.52
, Issue.21
, pp. 4709-4712
-
-
Anthoni, U.1
Chevolot, L.2
Larsen, C.3
Nielsen, P.H.4
Christophersen, C.5
-
29
-
-
70349920648
-
Highly enantioselective intramolecular aza-spiroannulation onto indoles using chiral rhodium catalysis: Asymmetric entry to the spiro-β-lactam core of chartellines
-
Sato A, Shibuya M, Kanoh N, Iwabuchi Y: Highly enantioselective intramolecular aza-spiroannulation onto indoles using chiral rhodium catalysis: Asymmetric entry to the spiro-β-lactam core of chartellines. Chem Commun (2009) (41):6264-6266.
-
(2009)
Chem Commun
, vol.41
, pp. 6264-6266
-
-
Sato, A.1
Shibuya, M.2
Kanoh, N.3
Iwabuchi, Y.4
-
30
-
-
66249118690
-
Staudinger ketene-imine cycloaddition RCM approach to macrocyclic bisazetidinones
-
Ibrahim YA, Al-Azemi TF, El-Halim MDA, John E: Staudinger ketene-imine cycloaddition, RCM approach to macrocyclic bisazetidinones. J Org Chem (2009) 74(11):4305-4310.
-
(2009)
J Org Chem
, vol.74
, Issue.11
, pp. 4305-4310
-
-
Ibrahim, Y.A.1
Al-Azemi, T.F.2
Mda, E.3
John, E.4
-
31
-
-
70349667007
-
Generating complexity from simplicity: Pd-Catalyzed or Cu-promoted domino alkyne homocoupling/double [2+2] allenyne cycloaddition
-
Alcaide B, Almendros P, Aragoncillo C: Generating complexity from simplicity: Pd-Catalyzed or Cu-promoted domino alkyne homocoupling/double [2+2] allenyne cycloaddition. Chem Eur J (2009) 15(39):9987-9989.
-
(2009)
Chem Eur J
, vol.15
, Issue.39
, pp. 9987-9989
-
-
Alcaide, B.1
Almendros, P.2
Aragoncillo, C.3
-
32
-
-
53549097892
-
Synthesis and biological evaluation of bile acid dimers linked with 1, 2,3-triazole and bis-β-lactam
-
Vatmurge NS, Hazra BG, Pore VS, Shirazi F, Deshpande MV, Kadreppa S, Chattopadhyay S, Gonnade RG: Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam. Org Biomol Chem (2008) 6(20): 3823-3830.
-
(2008)
Org Biomol Chem
, vol.6
, Issue.20
, pp. 3823-3830
-
-
Vatmurge, N.S.1
Hazra, B.G.2
Pore, V.S.3
Shirazi, F.4
Deshpande, M.V.5
Kadreppa, S.6
Chattopadhyay, S.7
Gonnade, R.G.8
-
33
-
-
0000727123
-
Asymmetric synthesis of building-blocks for peptides and peptidomimetics by means of the β-lactam synthon method
-
Ojima I, Delaloge F: Asymmetric synthesis of building-blocks for peptides and peptidomimetics by means of the β-lactam synthon method. Chem Soc Rev (1997) 26(5):377-386.
-
(1997)
Chem Soc Rev
, vol.26
, Issue.5
, pp. 377-386
-
-
Ojima, I.1
Delaloge, F.2
-
34
-
-
27844526992
-
Alkaloids from amphibian skin: A tabulation of over eight-hundred compounds
-
Daly JW, Spande TF, Garraffo HM: Alkaloids from amphibian skin: A tabulation of over eight-hundred compounds. J Nat Prod (2005) 68(11):1556-1575.
-
(2005)
J Nat Prod
, vol.68
, Issue.11
, pp. 1556-1575
-
-
Daly, J.W.1
Spande, T.F.2
Garraffo, H.M.3
-
35
-
-
0034607947
-
Sugar-mimic glycosidase inhibitors: Natural occurrence, biological activity and prospects for therapeutic application
-
Asano N, Nash RJ, Molyneux RJ, Fleet GWJ: Sugar-mimic glycosidase inhibitors: Natural occurrence, biological activity and prospects for therapeutic application. Tetrahedron Asymmetry (2000) 11(8):1645-1680.
-
(2000)
Tetrahedron Asymmetry
, vol.11
, Issue.8
, pp. 1645-1680
-
-
Asano, N.1
Nash, R.J.2
Molyneux, R.J.3
Gwj, F.4
-
36
-
-
77954770936
-
Ring expansion versus cyclization in 4-oxoazetidine-2-carbaldehydes catalyzed by molecular iodine: Experimental and theoretical study in concert
-
Alcaide B, Almendros P, Cabrero G, Ruiz MP, Arnó M, Domingo LR: Ring expansion versus cyclization in 4-oxoazetidine-2-carbaldehydes catalyzed by molecular iodine: Experimental and theoretical study in concert. Adv Synth Cat (2010) 352(10):1688-1700.
-
(2010)
Adv Synth Cat
, vol.352
, Issue.10
, pp. 1688-1700
-
-
Alcaide, B.1
Almendros, P.2
Cabrero, G.3
Ruiz, M.P.4
Arnó, M.5
Domingo, L.R.6
-
37
-
-
64349109494
-
Diastereoselective synthesis of bicyclic γ-lactams via ring expansion of monocyclic β-lactams
-
Dekeukeleire S, D'hooghe M, De Kimpe N: Diastereoselective synthesis of bicyclic γ-lactams via ring expansion of monocyclic β-lactams. J Org Chem (2009) 74(4):1644-1649.
-
(2009)
J Org Chem
, vol.74
, Issue.4
, pp. 1644-1649
-
-
Dekeukeleire, S.1
D'Hooghe, M.2
De Kimpe, N.3
-
38
-
-
0035756986
-
Chemistry and chemical biology of taxane anticancer agents
-
Miller ML, Ojima I: Chemistry and chemical biology of taxane anticancer agents. Chem Rec (2001) 1(3):195-211.
-
(2001)
Chem Rec
, vol.1
, Issue.3
, pp. 195-211
-
-
Miller, M.L.1
Ojima, I.2
-
39
-
-
75649147768
-
Total synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin
-
Paterson I, Naylor GJ, Fujita T, Guzmán E, Wright AE: Total synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin. Chem Commun (2010) 46(2):261-263.
-
(2010)
Chem Commun
, vol.46
, Issue.2
, pp. 261-263
-
-
Paterson, I.1
Naylor, G.J.2
Fujita, T.3
Guzmán, E.4
Wright, A.E.5
-
40
-
-
62349105131
-
Azide-free synthesis of oseltamivir from l-methionine
-
Oshitari T, Mandai T: Azide-free synthesis of oseltamivir from l-methionine. Synlett (2009) (5):787-789.
-
(2009)
Synlett
, vol.5
, pp. 787-789
-
-
Oshitari, T.1
Mandai, T.2
-
41
-
-
0000821873
-
Structure of kainic acid and its isomer, allokainic acid
-
Nitta I, Watase H, Tomiie Y: Structure of kainic acid and its isomer, allokainic acid. Nature (London) (1958) 181(4611): 761-762.
-
(1958)
Nature (London)
, vol.181
, Issue.4611
, pp. 761-762
-
-
Nitta, I.1
Watase, H.2
Tomiie, Y.3
-
42
-
-
20344388665
-
Kainic acid-mediated excitotoxicity as a model for neurodegeneration
-
Wang Q, Yu S, Simonyi A, Sun GY, Sun AY: Kainic acid-mediated excitotoxicity as a model for neurodegeneration. Mol Neurobiol (2005) 31(1-3):3-16.
-
(2005)
Mol Neurobiol
, vol.31
, Issue.1-3
, pp. 3-16
-
-
Wang, Q.1
Yu, S.2
Simonyi, A.3
Sun, G.Y.4
Sun, A.Y.5
-
43
-
-
48849098730
-
Total synthesis of (-)-kainic acid via intramolecular Michael addition: A second-generation route
-
Sakahuchi H, Tokuyama H, Fukuyama T: Total synthesis of (-)-kainic acid via intramolecular Michael addition: A second-generation route. Org Lett (2008) 10(9):1711-1714.
-
(2008)
Org Lett
, vol.10
, Issue.9
, pp. 1711-1714
-
-
Sakahuchi, H.1
Tokuyama, H.2
Fukuyama, T.3
-
44
-
-
1642465382
-
(+)- and (-)-syn-2-isobutyl-4-methylazetidine-2,4-dicarboxylic acids from the extract of Monascus pilosus-fermented rice (red-mold rice)
-
Akihisa T, Mafune S, Ukiya M, Kimura Y, Yasukawa K, Suzuki T, Tokuda H, Tanabe N, Fukuoka T: (+)- and (-)-syn-2-isobutyl-4-methylazetidine-2,4- dicarboxylic acids from the extract of Monascus pilosus-fermented rice (red-mold rice). J Nat Prod (2004) 67(3):479-480.
-
(2004)
J Nat Prods
, vol.67
, Issue.3
, pp. 479-480
-
-
Akihisa, T.1
Mafune, S.2
Ukiya, M.3
Kimura, Y.4
Yasukawa, K.5
Suzuki, T.6
Tokuda, H.7
Tanabe, N.8
Fukuoka, T.9
-
45
-
-
0000913103
-
Azetidines and bisazetidines. Their synthesis and use as the key intermediates to enantiomerically pure diamines, amino alcohols, and polyamines
-
Ojima I, Zhao M, Yamato T, Nakahashi K, Yamashita M, Abe R: Azetidines and bisazetidines. Their synthesis and use as the key intermediates to enantiomerically pure diamines, amino alcohols, and polyamines. J Org Chem (1991) 65(18):5263-5277.
-
(1991)
J Org Chem
, vol.65
, Issue.18
, pp. 5263-5277
-
-
Ojima, I.1
Zhao, M.2
Yamato, T.3
Nakahashi, K.4
Yamashita, M.5
Abe, R.6
-
46
-
-
70349784874
-
Direct anti-selective catalytic asymmetric Mannich-type reactions of α-ketoanilides for the synthesis of γ-amino amides and azetidine-2-amides
-
Xu Y, Lu G, Matsunaga S, Shibasaki M: Direct anti-selective catalytic asymmetric Mannich-type reactions of α-ketoanilides for the synthesis of γ-amino amides and azetidine-2-amides. Angew Chem Int Ed (2009) 48(18): 3353-3356.
-
(2009)
Angew Chem Int Ed
, vol.48
, Issue.18
, pp. 3353-3356
-
-
Xu, Y.1
Lu, G.2
Matsunaga, S.3
Shibasaki, M.4
-
47
-
-
0000918065
-
A new amino acid, nicotianamine, from tobacco leaves
-
Noma M, Noguchi M, Tamaki E: A new amino acid, nicotianamine, from tobacco leaves. Tetrahedron Lett (1971) 12(22):2017-2020.
-
(1971)
Tetrahedron Lett
, vol.12
, Issue.22
, pp. 2017-2020
-
-
Noma, M.1
Noguchi, M.2
Tamaki, E.3
-
48
-
-
41849144509
-
Novel antibacterial azetidine lincosamides
-
O'Dowd H, Lewis JG, Trias J, Asano R, Blais J, Lopez SL, Park GK, Wu C, Wang W, Gordeev MF: Novel antibacterial azetidine lincosamides. Bioorg Med Chem Lett (2008) 18(8):2645-2648.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, Issue.8
, pp. 2645-2648
-
-
O'Dowd, H.1
Lewis, J.G.2
Trias, J.3
Asano, R.4
Blais, J.5
Lopez, S.L.6
Park, G.K.7
Wu, C.8
Wang, W.9
Gordeev, M.F.10
-
49
-
-
66449102715
-
Direct access to l-azetidine-2-carboxylic acid
-
Bouazaoui M, Martinez J, Cavelier F: Direct access to l-azetidine-2-carboxylic acid. Eur J Org Chem (2009) (17): 2729-2732.
-
(2009)
Eur J Org Chem
, vol.17
, pp. 2729-2732
-
-
Bouazaoui, M.1
Martinez, J.2
Cavelier, F.3
-
50
-
-
38549086843
-
A facile synthesis of 1-arenesulfonyl-azetidines through reaction of 1-arenesulfonylaziridines with dimethylsulfoxonium methylide generated under microwave irradiation
-
Malik S, Nadir UK: A facile synthesis of 1-arenesulfonyl-azetidines through reaction of 1-arenesulfonylaziridines with dimethylsulfoxonium methylide generated under microwave irradiation. Synlett (2008) (1):108-110.
-
(2008)
Synlett
, vol.1
, pp. 108-110
-
-
Malik, S.1
Nadir, U.K.2
-
51
-
-
62049083037
-
1 antagonist for the treatment of obesity
-
1 antagonist for the treatment of obesity. Tetrahedron (2009) 65(16):3292-3304.
-
(2009)
Tetrahedron
, vol.65
, Issue.16
, pp. 3292-3304
-
-
Brandt, T.A.1
Caron, S.2
Damon, D.B.3
Dibrino, J.4
Ghosh, A.5
Griffth, D.A.6
Kedia, S.7
Ragan, J.A.8
Rose, P.R.9
Vanderplas, B.C.10
Wei, L.11
-
52
-
-
77951860659
-
Synthesis and structural analysis of a new class of azaspiro[ 3.3]heptanes as building blocks for medicinal chemistry
-
Burkhard JA, Guérot C, Knust H, Rogers-Evans M, Carreria EM: Synthesis and structural analysis of a new class of azaspiro[3.3]heptanes as building blocks for medicinal chemistry. Org Lett (2010) 12(9):1944-1947.
-
(2010)
Org Lett
, vol.12
, Issue.9
, pp. 1944-1947
-
-
Burkhard, J.A.1
Guérot, C.2
Knust, H.3
Rogers-Evans, M.4
Carreria, E.M.5
-
53
-
-
77952381703
-
Synthesis of azaspirocycles and their evaluation in drug discovery
-
Burkhard JA, Wagner B, Fisher H, Schuler F, Müller K, Carreira EM: Synthesis of azaspirocycles and their evaluation in drug discovery. Angew Chem Int Ed (2010) 49(20):3524-3527.
-
(2010)
Angew Chem Int Ed
, vol.49
, Issue.20
, pp. 3524-3527
-
-
Burkhard, J.A.1
Wagner, B.2
Fisher, H.3
Schuler, F.4
Müller, K.5
Carreira, E.M.6
-
54
-
-
77950863934
-
3 receptor antagonists
-
3 receptor antagonists. Bioorg Med Chem Lett (2010) 20(9): 2755-2760.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, Issue.9
, pp. 2755-2760
-
-
Stocking, E.M.1
Aluisio, L.2
Atack, J.R.3
Bonaventure, P.4
Carruthers, N.I.5
Dugovic, C.6
Everson, A.7
Fraser, I.8
Jiang, X.9
Leung, P.10
Lord, B.11
-
55
-
-
77954216576
-
Design, synthesis and evaluation of 2,4-disubstituted pyrimidines as cholinesterase inhibitors
-
Mohamed T, Rao PPN: Design, synthesis and evaluation of 2,4-disubstituted pyrimidines as cholinesterase inhibitors. Bioorg Med Chem Lett (2010) 20(12):3606-3609.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, Issue.12
, pp. 3606-3609
-
-
Mohamed, T.1
Ppn, R.2
-
56
-
-
45749106438
-
Rearrangement of 2-hydroxyalkylazetidines into 3-fuoropyrrolidines
-
Drouillat B, Couty F, David O, Evano G, Marrot J: Rearrangement of 2-hydroxyalkylazetidines into 3-fuoropyrrolidines. Synlett (2008) (9):1345-1348.
-
(2008)
Synlett
, vol.9
, pp. 1345-1348
-
-
Drouillat, B.1
Couty, F.2
David, O.3
Evano, G.4
Marrot, J.5
-
57
-
-
58349085081
-
2-mediated nucleophilic ring-opening followed by the [4+2] cycloaddition of N-tosylazetidines with nitriles
-
2-mediated nucleophilic ring-opening followed by the [4+2] cycloaddition of N-tosylazetidines with nitriles. Tetrahedron Lett (2009) 50(10):1105-1109.
-
(2009)
Tetrahedron Lett
, vol.50
, Issue.10
, pp. 1105-1109
-
-
Ghorai, M.K.1
Das, K.2
Kumar, A.3
-
58
-
-
72049106106
-
Ring expansion of 2-alkenyl azetidines into unsaturated azocanes
-
Drouillat B, Couty F, Razafmahaléo V: Ring expansion of 2-alkenyl azetidines into unsaturated azocanes. Synlett (2009) (19):3182-3186.
-
(2009)
Synlett
, vol.19
, pp. 3182-3186
-
-
Drouillat, B.1
Couty, F.2
Razafmahaléo, V.3
-
59
-
-
62349140232
-
First example of C-3 alkylation of indoles with activated azetidines catalyzed by indium(III) bromide
-
Yadav JS, Subba Reddy BV, Narasimhulu G, Satheesh G: First example of C-3 alkylation of indoles with activated azetidines catalyzed by indium(III) bromide. Synlett (2009) (5):727-730.
-
(2009)
Synlett
, vol.5
, pp. 727-730
-
-
Yadav, J.S.1
Subba Reddy, B.V.2
Narasimhulu, G.3
Satheesh, G.4
|