-
1
-
-
79957583046
-
-
For review, see:, Ed. Academic Press: London, UK, (and previous volumes)
-
For review, see: Katritzky, A.R., Ed. Advances in Heterocyclic Chemistry; Academic Press: London, UK, 2011; Volume 102 (and previous volumes).
-
Advances in Heterocyclic Chemistry
, vol.102
, pp. 2011
-
-
Katritzky, A.R.1
-
2
-
-
84883545226
-
-
For another review, see, Eds. Elsevier: Oxford, UK, (and previous volumes)
-
For another review, see: Gribble, G.W., Joule, J.A., Eds. Progress in Heterocyclic Chemistry; Elsevier: Oxford, UK, 2011; Volume 22 (and previous volumes).
-
(2011)
Progress in Heterocyclic Chemistry
, vol.22
-
-
Gribble, G.W.1
Joule, J.A.2
-
3
-
-
78149305896
-
Comprehensive survey of chemical libraries for drug discovery and chemical biology
-
Dolle, R.E.; Le Bourdonnec, B.; Worm, K.; Morales, G.A.; Thomas, C.J.; Zhang, W. Comprehensive Survey of Chemical Libraries for Drug Discovery and Chemical Biology. J. Comb. Chem. 2010, 12, 765-806.
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 765-806
-
-
Dolle, R.E.1
Le Bourdonnec, B.2
Worm, K.3
Morales, G.A.4
Thomas, C.J.5
Zhang, W.6
-
5
-
-
0034678033
-
Target-oriented and diversity-oriented organic synthesis in drug discovery
-
DOI 10.1126/science.287.5460.1964
-
Schreiber, S.L. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery. Science 2000, 287, 1964-1969. (Pubitemid 30158663)
-
(2000)
Science
, vol.287
, Issue.5460
, pp. 1964-1969
-
-
Schreiber, S.L.1
-
6
-
-
37549020046
-
Towards the optimal screening collection: A synthesis strategy
-
Nielsen, T.E.; Schreiber, S.L. Towards the Optimal Screening Collection: A Synthesis Strategy. Angew. Chem. Int. Ed. Engl. 2008, 47, 48-56.
-
(2008)
Angew. Chem. Int. Ed. Engl
, vol.47
, pp. 48-56
-
-
Nielsen, T.E.1
Schreiber, S.L.2
-
7
-
-
84880296641
-
Diversity-oriented synthesis as a tool for the discovery of novel biologically functional small molecules
-
Galloway, W.R.J.D.; Isidro-Llobet, A.; Spring, D.R. Diversity-oriented synthesis as a tool for the discovery of novel biologically functional small molecules. Nat. Commun. 2010, 1, 80-92.
-
(2010)
Nat. Commun.
, vol.1
, pp. 80-92
-
-
Galloway, W.R.J.D.1
Isidro-Llobet, A.2
Spring, D.R.3
-
8
-
-
84891316538
-
-
Eds. Wiley-VCH: Weinheim, Germany
-
Schreiber, S.L., Kapoor, T.M., Wess, G., Eds. Chemical Biology: From Small Molecules to Systems Biology and Drug Design; Wiley-VCH: Weinheim, Germany, 2008.
-
(2008)
Chemical Biology: From Small Molecules to Systems Biology and Drug Design
-
-
Schreiber, S.L.1
Kapoor, T.M.2
Wess, G.3
-
9
-
-
0037432765
-
From knowing to controlling: A path from genomics to drugs using small molecule probes
-
DOI 10.1126/science.1083395
-
Strausberg, R.L.; Schreiber, S.L. From knowing to controlling: A path from genomics to drugs using small molecule probes. Science 2003, 300, 294-295. (Pubitemid 36433713)
-
(2003)
Science
, vol.300
, Issue.5617
, pp. 294-295
-
-
Strausberg, R.L.1
Schreiber, S.L.2
-
11
-
-
0037462076
-
An expedient phosphine-catalyzed [4 + 2] annulation: Synthesis of highly functionalized tetrahydropyridines
-
DOI 10.1021/ja0344009
-
Zhu, X.; Lan, J.; Kwon, O. An Expedient Phosphine-Catalyzed [4 + 2] Annulation: Synthesis of Highly Functionalized Tetrahydropyridiness. J. Am. Chem. Soc. 2003, 125, 4716-4717. (Pubitemid 36505358)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.16
, pp. 4716-4717
-
-
Zhu, X.-F.1
Lan, J.2
Kwon, O.3
-
12
-
-
20444447549
-
A highly diastereoselective synthesis of 3-carbethoxy-2,5-disubstituted- 3- pyrrolines by phosphine catalysis
-
DOI 10.1016/j.tet.2005.03.104, PII S0040402005006071, Applications of Catalysis in Academia and Industry
-
Zhu, X.; Henry, C.E.; Kwon, O. A highly diastereoselective synthesis of 3-carbethoxy-2,5- disubstituted-3-pyrrolines by phosphine catalysis. Tetrahedron 2005, 61, 6276-6282. (Pubitemid 40812982)
-
(2005)
Tetrahedron
, vol.61
, Issue.26
, pp. 6276-6282
-
-
Zhu, X.-F.1
Henry, C.E.2
Kwon, O.3
-
13
-
-
17444432653
-
A phosphine-catalyzed synthesis of 1,3- dioxan-4-ylidenes
-
Zhu, X.; Henry, C.E.; Wang, J.; Dudding, T.; Kwon, O. A Phosphine-Catalyzed Synthesis of 1,3- Dioxan-4-ylidenes. Org. Lett. 2005, 7, 1387-1390.
-
(2005)
Org. Lett
, vol.7
, pp. 1387-1390
-
-
Zhu, X.1
Henry, C.E.2
Wang, J.3
Dudding, T.4
Kwon, O.5
-
14
-
-
22244458282
-
Phosphine-catalyzed synthesis of 6-substituted 2-pyrones: Manifestation of E/Z-isomerism in the zwitterionic intermediate
-
DOI 10.1021/ol050946j
-
Zhu, X.; Schaffner, A.; Li, R.C.; Kwon, O. Phosphine-Catalyzed Synthesis of 6-Substituted 2-Pyrones: Manifestation of E/Z-Isomerism in the Zwitterionic Intermediate. Org. Lett. 2005, 7, 2977-2980. (Pubitemid 40992611)
-
(2005)
Organic Letters
, vol.7
, Issue.14
, pp. 2977-2980
-
-
Zhu, X.-F.1
Schaffner, A.-P.2
Li, R.C.3
Kwon, O.4
-
15
-
-
34248575467
-
Small-molecule inhibitors of protein geranylgeranyltransferase type I
-
DOI 10.1021/ja070274n
-
Castellano, S.; Fiji, H.D.G.; Kinderman, S.S.; Watanabe, M.; De Leon, P.; Tamanoi, F.; Kwon, O. Small-Molecule Inhibitors of Protein Geranylgeranyltransferase Type I. J. Am. Chem. Soc. 2007, 129, 5843-5845. (Pubitemid 46748488)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.18
, pp. 5843-5845
-
-
Castellano, S.1
Fiji, H.D.G.2
Kinderman, S.S.3
Watanabe, M.4
De Leon, P.5
Tamanoi, F.6
Kwon, O.7
-
16
-
-
34547957084
-
Phosphine-catalyzed synthesis of highly functionalized coumarins
-
Henry, C.E.; Kwon, O. Phosphine-Catalyzed Synthesis of Highly Functionalized Coumarins. Org. Lett. 2007, 9, 3069-3072.
-
(2007)
Org. Lett
, vol.9
, pp. 3069-3072
-
-
Henry, C.E.1
Kwon, O.2
-
17
-
-
35548965614
-
Phosphine-catalyzed [4 + 2] annulation: Synthesis of cyclohexenes
-
DOI 10.1021/ja0752181
-
Tran, Y.S.; Kwon, O. Phosphine-Catalyzed [4 + 2] Annulation: Synthesis of Cyclohexenes. J. Am. Chem. Soc. 2007, 129, 12632-12633. (Pubitemid 350004451)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.42
, pp. 12632-12633
-
-
Tran, Y.S.1
Kwon, O.2
-
18
-
-
38949177006
-
Alcohol-assisted phosphine catalysis: One-step synthesis of dihydropyrone from aldehyde and allenoate
-
Creech, G.S.; Kwon, O. Alcohol-Assisted Phosphine Catalysis: One-Step Synthesis of Dihydropyrone from Aldehyde and Allenoate. Org. Lett. 2008, 10, 429-432.
-
(2008)
Org. Lett
, vol.10
, pp. 429-432
-
-
Creech, G.S.1
Kwon, O.2
-
19
-
-
44349178715
-
Inhibitors of protein geranylgeranyltransferase-I and rab geranylgeranyltransferase identified from a library of allenoate derived compounds
-
Watanabe, M.; Fiji, H.D.G.; Guo, L.; Umetsu, A.; Kinderman, S.S.; Slamon, D.J.; Kwon, O.; Tamanoi, F. Inhibitors of protein geranylgeranyltransferase-I and Rab geranylgeranyltransferase identified from a library of allenoate derived compounds. J. Biol. Chem. 2008, 283, 9571-9579.
-
(2008)
J. Biol. Chem
, vol.283
, pp. 9571-9579
-
-
Watanabe, M.1
Fiji, H.D.G.2
Guo, L.3
Umetsu, A.4
Kinderman, S.S.5
Slamon, D.J.6
Kwon, O.7
Tamanoi, F.8
-
20
-
-
51749125933
-
Theory-guided design of bronsted acid-assisted phosphine catalysis: Synthesis of dihydropyrones from aldehydes and allenoates
-
Creech, G.S.; Zhu, X.; Fonovic, B.; Dudding, T.; Kwon, O. Theory-Guided Design of Brønsted Acid-Assisted Phosphine Catalysis: Synthesis of Dihydropyrones from Aldehydes and Allenoates Tetrahedron 2008, 64, 6935-6942.
-
(2008)
Tetrahedron
, vol.64
, pp. 6935-6942
-
-
Creech, G.S.1
Zhu, X.2
Fonovic, B.3
Dudding, T.4
Kwon, O.5
-
21
-
-
66849109067
-
In vivo anticancer effect of a novel inhibitor of protein geranylgeranyltransferase I
-
Lu, J.; Chan, L.; Fiji, H.D.G.; Dahl, R.; Kwon, O.; Tamanoi, F. In vivo anticancer effect of a novel inhibitor of protein geranylgeranyltransferase I. Mol. Cancer Ther. 2009, 8, 1218-1226.
-
(2009)
Mol. Cancer Ther
, vol.8
, pp. 1218-1226
-
-
Lu, J.1
Chan, L.2
Fiji, H.D.G.3
Dahl, R.4
Kwon, O.5
Tamanoi, F.6
-
22
-
-
69949162395
-
Phosphine-promoted [3+3] annulation of aziridines with allenoates: A facile enrty into highly functionalized tetrahydropyridines
-
Guo, H.; Xu, Q.; Kwon, O. Phosphine-Promoted [3+3] Annulation of Aziridines with Allenoates: A Facile Enrty into Highly Functionalized Tetrahydropyridines. J. Am. Chem. Soc. 2009, 131, 6318-6319.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 6318-6319
-
-
Guo, H.1
Xu, Q.2
Kwon, O.3
-
23
-
-
78649559846
-
Phosphine-catalyzed [4+2] annulation: Synthesis of ethyl 6-phenyl-1-tosyl- 1 2 5,6-tetrahydropyridine-3-carboxylate
-
Lu, K.; Kwon, O. Phosphine-catalyzed [4+2] Annulation: Synthesis of Ethyl 6-phenyl-1-tosyl- 1,2,5,6-tetrahydropyridine-3-carboxylate. Org. Synth. 2009, 86, 212-224.
-
(2009)
Org. Synth
, vol.86
, pp. 212-224
-
-
Lu, K.1
Kwon, O.2
-
24
-
-
77954244086
-
Equilibria between vinylogous ylides phosphonium dienolate Zwitterions: Vinylogous wittig olefination versus vinylogous aldol-type reactions
-
Khong, S.N.; Tran, Y.S.; Kwon, O. Equilibria Between Vinylogous Ylides and Phosphonium Dienolate Zwitterions: Vinylogous Wittig Olefination Versus Vinylogous Aldol-Type Reactions. Tetrahedron 2010, 66, 4760-4768.
-
(2010)
Tetrahedron
, vol.66
, pp. 4760-4768
-
-
Khong, S.N.1
Tran, Y.S.2
Kwon, O.3
-
25
-
-
78651247094
-
Diversity via a branched reaction pathway: Generation of a library of sixteen muticyclic scaffolds and identification of anti-migratory agents
-
Wang, Z.; Castellano, S.; Kinderman, S.S.; Argueta, C.E.; Beshir, A.B.; Fenteany, G.; Kwon, O. Diversity via a Branched Reaction Pathway: Generation of A Library of Sixteen Muticyclic Scaffolds and Identification of Anti-Migratory Agents. Chem. Eur. J. 2011, 17, 649-654.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 649-654
-
-
Wang, Z.1
Castellano, S.2
Kinderman, S.S.3
Argueta, C.E.4
Beshir, A.B.5
Fenteany, G.6
Kwon, O.7
-
26
-
-
79957584807
-
Phosphine catalyzed [3+2] annulation: Synthesis of ethyl 5-(tert- Butyl)-2-phenyl-1-Tosyl-3-Pyrroline-3-Carboxylate
-
Andrews, I.P.; Kwon, O. Phosphine Catalyzed [3+2] Annulation: Synthesis of Ethyl 5-(tert- Butyl)-2-phenyl-1-Tosyl-3-Pyrroline-3-Carboxylate. Org. Synth. 2011, 88, 138-151.
-
(2011)
Org. Synth.
, vol.88
, pp. 138-151
-
-
Andrews, I.P.1
Kwon, O.2
-
27
-
-
79955134993
-
Alplexone targets the hmg-coa reductase pathway and differentially regulates arteriovenous angiogenesis
-
Choi, J.; Mouillesseauex, K.; Wang, Z.; Fiji, H.D.G.; Kinderman, S.S.; Otto, G.W.; Geisler, R.; Kwon, O.; Chen, J.-N. Alplexone Targets the HMG-CoA Reductase Pathway and Differentially Regulates Arteriovenous Angiogenesis. Development 2011, 138, 1173-1182.
-
(2011)
Development
, vol.138
, pp. 1173-1182
-
-
Choi, J.1
Mouillesseauex, K.2
Wang, Z.3
Fiji, H.D.G.4
Kinderman, S.S.5
Otto, G.W.6
Geisler, R.7
Kwon, O.8
Chen, J.-N.9
-
28
-
-
79955568049
-
Diversity through phosphine catalysis identifies octahydro-1,6- naphthyridin-4-ones as activators of endothelium-driven innate immunity
-
Cruz, D.; Wang, Z.; Kibbie, J.; Modlin, R.; Kwon, O. Diversity through phosphine catalysis identifies octahydro-1,6-naphthyridin-4-ones as activators of endothelium-driven innate immunity. Proc. Natl. Acad. Sci. USA 2011, 108, 6769-6774.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 6769-6774
-
-
Cruz, D.1
Wang, Z.2
Kibbie, J.3
Modlin, R.4
Kwon, O.5
-
29
-
-
79956155927
-
Phosphine-Catalyzed β'-Umpolung Addition of Activated α-Alkyl Allenes
-
DOI:10.1021/ol200697m
-
Martin, T.J.; Tran, Y.S.; Vakhshori, V.G.; Kwon, O. Phosphine-Catalyzed β'-Umpolung Addition of Activated α-Alkyl Allenes. Org. Lett. 2011, DOI:10.1021/ol200697m.
-
(2011)
Org. Lett.
-
-
Martin, T.J.1
Tran, Y.S.2
Vakhshori, V.G.3
Kwon, O.4
-
30
-
-
35848957043
-
Bisphosphine-catalyzed mixed double-Michael reactions: Asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines
-
DOI 10.1021/ja073754n
-
Vardhineedi, S.; Barcan, G.A.; Kwon, O. Bisphosphine-Catalyzed Mixed Double-Michael Reactions: Asymmetric Synthesis of Oxazolidines, Thiazolidines, and Pyrrolidines. J. Am. Chem. Soc. 2007, 129, 12928-12929. (Pubitemid 350058321)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.43
, pp. 12928-12929
-
-
Sriramurthy, V.1
Barcan, G.A.2
Kwon, O.3
-
31
-
-
77749280142
-
Diphosphine-catalyzed mixed double-michael reaction: A unified synthesis of indolines, dihydropyrrolopyridines, benzimidazolines, tetrahydroquinolines, tetrahydroisoquinolines, dihydrobenzo-1,4-oxazines, and dihydrobenzo-3,1- oxazines
-
Vardhineedi, S.; Kwon, O. Diphosphine-Catalyzed Mixed Double-Michael Reaction: A Unified Synthesis of Indolines, Dihydropyrrolopyridines, Benzimidazolines, Tetrahydroquinolines, Tetrahydroisoquinolines, Dihydrobenzo-1,4-oxazines, and Dihydrobenzo-3,1-oxazines. Org. Lett. 2010, 12, 1084-1087.
-
(2010)
Org. Lett.
, vol.12
, pp. 1084-1087
-
-
Vardhineedi, S.1
Kwon, O.2
-
32
-
-
0002805292
-
Michael additions catalyzed by phosphines. An overlooked synthetic method
-
White, D.A.; Baizer, M.M. Michael additions catalyzed by phosphines. An overlooked synthetic method. Tetrahedron Lett. 1973, 14, 3597-3600.
-
(1973)
Tetrahedron Lett
, vol.14
, pp. 3597-3600
-
-
White, D.A.1
Baizer, M.M.2
-
33
-
-
0002074053
-
Organic synthesis with trialkylphosphine catalysts. Conjugate addition of alcohols to α,β-unsaturated alkynic acid esters
-
Inanaga, J.; Baba, Y.; Hanamoto, T. Organic Synthesis with Trialkylphosphine Catalysts. Conjugate Addition of Alcohols to α,β-Unsaturated Alkynic Acid Esters. Chem. Lett. 1993, 2, 241-244.
-
(1993)
Chem. Lett
, vol.2
, pp. 241-244
-
-
Inanaga, J.1
Baba, Y.2
Hanamoto, T.3
-
34
-
-
0033578687
-
[n + 1] Annulation route to highly substituted cyclic ketones with pendent ketone nitrile, and ester functionality
-
Grossman, R.B.; Pendharkar, D.S.; Patrick, B.O. [n + 1] Annulation Route to Highly Substituted Cyclic Ketones with Pendent Ketone, Nitrile, and Ester Functionality. J. Org. Chem. 1999, 64, 7178-7183.
-
(1999)
J. Org. Chem
, vol.64
, pp. 7178-7183
-
-
Grossman, R.B.1
Pendharkar, D.S.2
Patrick, B.O.3
-
35
-
-
0037423171
-
Phosphoramidites are efficient, green organocatalysts for the Michael reaction. Mechanistic insights into the phosphorus-catalyzed Michael reaction of alkynones and implications for asymmetric catalysis
-
DOI 10.1021/jo026425g
-
Grossan, R.B.; Comesse, S.; Rasne, R.M.; Hattori, K.; Delong, M.N. Phosphoramidites Are Efficient, Green Organocatalysts for the Michael Reaction. Mechanistic Insights into the Phosphorous-Catalyzed Michael Reaction of Alkynones and Implications for Asymmetric Catalysis. J. Org. Chem. 2003, 68, 871-874. (Pubitemid 36176609)
-
(2003)
Journal of Organic Chemistry
, vol.68
, Issue.3
, pp. 871-874
-
-
Grossman, R.B.1
Comesse, S.2
Rasne, R.M.3
Hattori, K.4
Delong, M.N.5
-
36
-
-
33750089005
-
Vinylphosphonium salt mediated reaction between alkyl propiolates and aminophenols or hydroxyphenols
-
DOI 10.1055/s-2006-950230
-
Yavari, I.; Souri, S.; Sirouspour, M.; Djahaniani, H. Vinylphosphonium Salt Mediated Reaction between Alkyl Propiolates and Aminophenols or Hydroxyphenols. Synthesis 2006, 3243-3249. (Pubitemid 44578090)
-
(2006)
Synthesis
, Issue.19
, pp. 3243-3249
-
-
Yavari, I.1
Souri, S.2
Sirouspour, M.3
Djahaniani, H.4
-
37
-
-
79957587356
-
-
Dithianes can be formed through the double-Michael reaction of propane 1,3-dithiol in the presence of bases (e.g., NaOMe, NaOEt, NBu4OH)
-
Dithianes can be formed through the double-Michael reaction of propane 1,3-dithiol in the presence of bases (e.g., NaOMe, NaOEt, NBu4OH);
-
-
-
-
38
-
-
0041375503
-
Development of β-keto 1,3-dithianes as versatile intermediates for organic synthesis
-
see: Gaunt, M.J.; Sneddon, H.F.; Hewitt, P.R.; Orsini, P.; Hook, D.F.; Ley, S.V. Development of β-keto 1,3-dithianes as versatile intermediates for organic synthesis. Org. Bimol. Chem. 2003, 1, 15-16.
-
(2003)
Org. Bimol. Chem
, vol.1
, pp. 15-16
-
-
Gaunt, M.J.1
Sneddon, H.F.2
Hewitt, P.R.3
Orsini, P.4
Hook, D.F.5
Ley, S.V.6
-
39
-
-
0037181364
-
Total synthesis of (-)-tetrazomine. Determination of the stereochemistry of tetrazomine and the synthesis and biological activity of tetrazomine analogues
-
DOI 10.1021/ja0174027
-
Scott, J.D.; Williams, R.M. Total Synthesis of (-)-Tetrazomine. Determination of the Stereochemistry of Tetrazomine and the Synthesis and Biological Activity of tetrazomine Analogues. J. Am. Chem. Soc. 2002, 124, 2951-2956. (Pubitemid 34249971)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.12
, pp. 2951-2956
-
-
Scott, J.D.1
Williams, R.M.2
-
40
-
-
0034005126
-
Synthesis of a netropsin conjugate of a water-soluble epi-quinocarcin analogue: The importance of stereochemistry at nitrogen
-
DOI 10.1016/S0968-0896(99)00314-4, PII S0968089699003144
-
Herberich, B.; Scott, J.D.; Williams, R.M. Synthesis of a netropsin conjugate of a water-soluble epi-quinocarcin analogue: The importance of stereochemistry at nitrogen. Bioorg. Med. Chem. 2000, 8, 523-532. (Pubitemid 30122358)
-
(2000)
Bioorganic and Medicinal Chemistry
, vol.8
, Issue.3
, pp. 523-532
-
-
Herberich, B.1
Scott, J.D.2
Williams, R.M.3
-
41
-
-
0003445429
-
-
Eds, 2nd ed.; Springer: Berlin, Germany
-
Jacobsen, E.N., Pfaltz, A., Yamamoto, H., Eds. Comprehensive Asymmetric Catalysis I-III, 2nd ed.; Springer: Berlin, Germany, 1999.
-
(1999)
Comprehensive Asymmetric Catalysis I-III
-
-
Jacobsen, E.N.1
Pfaltz, A.2
Yamamoto, H.3
-
43
-
-
0033714636
-
Nitrogen-containing ligands for asymmetric homogeneous and heterogeneous catalysis
-
Fache, F.; Schultz, E.; Tommasino, M.L.; Lemaire, M. Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis. Chem. Rev. 2000, 100, 2159-2232.
-
(2000)
Chem. Rev
, vol.100
, pp. 2159-2232
-
-
Fache, F.1
Schultz, E.2
Tommasino, M.L.3
Lemaire, M.4
-
46
-
-
79952387553
-
Asymmetric catalysis with chiral oxazolidine ligands
-
Wolf, C.; Xu, H. Asymmetric catalysis with chiral oxazolidine ligands. Chem. Commun. 2011, 47, 3339-3350.
-
(2011)
Chem. Commun.
, vol.47
, pp. 3339-3350
-
-
Wolf, C.1
Xu, H.2
-
47
-
-
33846615885
-
Highly efficient synthesis of enantiomerically enriched 2-hydroxymethylaziridines by enzymatic desymmetrization
-
Characterization of 1d
-
Characterization of 1d: Choi, J.Y.; Borch, R.F. Highly Efficient Synthesis of Enantiomerically Enriched 2-Hydroxymethylaziridines by Enzymatic Desymmetrization. Org. Lett. 2007, 9, 215-218.
-
(2007)
Org. Lett
, vol.9
, pp. 215-218
-
-
Choi, J.Y.1
Borch, R.F.2
-
48
-
-
22144498455
-
A general method for the preparation of chiral TREN derivatives
-
DOI 10.1002/ejoc.200500094
-
Pei, Y.; Brade, K.; Brule, E.; Hagber, L.; Lake, F.; Moberg, C. A General Method for the Preparation of Chiral TREN Derivatives. Eur. J. Org. Chem. 2005, 2005, 2835-2840. (Pubitemid 40976849)
-
(2005)
European Journal of Organic Chemistry
, Issue.13
, pp. 2835-2840
-
-
Pei, Y.1
Brade, K.2
Brule, E.3
Hagberg, L.4
Lake, F.5
Moberg, C.6
-
49
-
-
85045552781
-
A convenient method for the preparation of enantiomerically pure 2-substituted N-tosylaziiridines
-
Berry, M.B.; Craig, D. A Convenient Method for the Preparation of Enantiomerically Pure 2-Substituted N-Tosylaziiridines. Synlett 1992, 41-44.
-
(1992)
Synlett
, pp. 41-44
-
-
Berry, M.B.1
Craig, D.2
-
50
-
-
41849088108
-
Hot water-promoted ring-opening of epoxides and aziridines by water and other nucleopliles
-
DOI 10.1021/jo702401t
-
Wang, Z.; Cui, Y.-T.; Xu, Z.-B.; Qu, J. Hot Water-Promoted Ring-Opening of Epoxides and Aziridines by Water and Other Nucleophiles. J. Org. Chem. 2008, 73, 2270-2274. (Pubitemid 351497756)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.6
, pp. 2270-2274
-
-
Wang, Z.1
Cui, Y.-T.2
Xu, Z.-B.3
Qu, J.4
-
51
-
-
0001683069
-
Metal(II) d-Tartrates catalyzed asymmetric ring opening of oxiranes with various nucleophiles
-
Yamashita, H. Metal(II) d-Tartrates Catalyzed Asymmetric Ring Opening of Oxiranes with Various Nucleophiles. Bull. Chem. Soc. Jpn. 1988, 61, 1213-1220.
-
(1988)
Bull. Chem. Soc. Jpn
, vol.61
, pp. 1213-1220
-
-
Yamashita, H.1
-
52
-
-
33645036043
-
Resolution of racemic 2-aminocyclohexanol derivatives and their application as lifands in asymmetric catalysis
-
Schiffers, I.; Rantanen, T.; Schmidt, F.; Bergmans, W.; Zani, L.; Bolm, C. Resolution of Racemic 2-Aminocyclohexanol Derivatives and Their Application as Lifands in Asymmetric Catalysis. J. Org. Chem. 2006, 71, 2320-2331.
-
(2006)
J. Org. Chem
, vol.71
, pp. 2320-2331
-
-
Schiffers, I.1
Rantanen, T.2
Schmidt, F.3
Bergmans, W.4
Zani, L.5
Bolm, C.6
-
53
-
-
35148854218
-
Direct diazo-transfer reaction on β-lactam: Synthesis and preliminary biological activities of 6-triazolylpenicillanic acids
-
DOI 10.1016/j.bmc.2007.08.035, PII S0968089607007304
-
Chen, P.C.; Wharton, R.E.; Patel, P.A.; Oyelere, A.K. Direct diazo-transfer reaction of β-lactam: Synthesis and preliminary biological activities of 6-triazolylpenicillanic acids. Bioorg. Med. Chem. 2007, 15, 7288-7300. (Pubitemid 47539148)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.23
, pp. 7288-7300
-
-
Chen, P.C.1
Wharton, R.E.2
Patel, P.A.3
Oyelere, A.K.4
-
54
-
-
0036020059
-
1A receptor ligands
-
DOI 10.1016/S0928-0987(02)00045-3, PII S0928098702000453
-
Calieno, G.; Fiorino, F.; Perissutti, E.; Severino, B.; Scolaro, D.; Gessi, S.; Cattabriga, E.; Borea, P.A.; Santagada, V. A convenient synthesis by microwave heating and pharmacological evaluation of novel benzoyltriazole and saccharine derivatives as 5-HT1A receptor ligands. Eur. J. Pharm. Sci. 2002, 16, 15-28. (Pubitemid 34756778)
-
(2002)
European Journal of Pharmaceutical Sciences
, vol.16
, Issue.1-2
, pp. 15-28
-
-
Caliendo, G.1
Fiorino, F.2
Perissutti, E.3
Severino, B.4
Scolaro, D.5
Gessi, S.6
Cattabriga, E.7
Borea, P.A.8
Santagada, V.9
-
55
-
-
34250631429
-
Rapid preparation of 3- Deoxyanthocyanidins and novel dicationic derivatives: New insight into an old procedure
-
Chassaing, S.; Kueny-Stotz, M.; Isorez, G.; Brouillard, R. Rapid Preparation of 3- Deoxyanthocyanidins and Novel Dicationic Derivatives: New Insight into an Old Procedure. Eur. J. Org. Chem. 2007, 38, 2438-2448.
-
(2007)
Eur. J. Org. Chem
, vol.38
, pp. 2438-2448
-
-
Chassaing, S.1
Kueny-Stotz, M.2
Isorez, G.3
Brouillard, R.4
-
56
-
-
0037144684
-
Oxovanadium complex-catalyzed aerobic oxidation of propargylic alcohols
-
Maeda, Y.; Kakiuchi, N.; Matsumura, S.; Nishimura, T.; Kawamura, T.; Uemura, S. Oxovanadium Complex-Catalyzed Aerobic Oxidation of Propargylic Alcohols. J. Org. Chem. 2002, 67, 6718-6724.
-
(2002)
J. Org. Chem
, vol.67
, pp. 6718-6724
-
-
Maeda, Y.1
Kakiuchi, N.2
Matsumura, S.3
Nishimura, T.4
Kawamura, T.5
Uemura, S.6
-
57
-
-
15244341085
-
Stereoselective synthesis of hex-2-(E)-en-4-yn-1,6-dioates and E,Z-muconic acid diesters via organo-catalyzed self-coupling of propiolates
-
DOI 10.1016/j.tetlet.2005.02.098
-
Ramachandran, P.V.; Rudd, M.T.; Reddy, M.V.R. Stereoselective synthesis of hex-2-(E)-en-4-yn- 1,6-dioates and E,Z-muconic acid diesters via organo-catalyzed self-coupling of propiolates. Tetrahedron Lett. 2005, 46, 2547-2549. (Pubitemid 40386409)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.15
, pp. 2547-2549
-
-
Ramachandran, P.V.1
Rudd, M.T.2
Reddy, M.V.R.3
-
58
-
-
0001720669
-
Improved preparation of aliphatic propynoic esters
-
Balas, L.; Jousseaume, B.; Langwost, B. Improved preparation of aliphatic propynoic esters. Tetrahedron Lett. 1989, 30, 4525-526.
-
(1989)
Tetrahedron Lett
, vol.30
, pp. 4525-526
-
-
Balas, L.1
Jousseaume, B.2
Langwost, B.3
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