-
1
-
-
0013844446
-
Automated Synthesis of Peptides
-
Merrifield, R. B. Automated Synthesis of Peptides Science 1965, 150, 178-185 10.1126/science.150.3693.178
-
(1965)
Science
, vol.150
, pp. 178-185
-
-
Merrifield, R.B.1
-
2
-
-
0022144562
-
Gene Synthesis Machines: DNA Chemistry and its Uses
-
Caruthers, M. H. Gene Synthesis Machines: DNA Chemistry and its Uses Science 1985, 230, 281-285 10.1126/science.3863253
-
(1985)
Science
, vol.230
, pp. 281-285
-
-
Caruthers, M.H.1
-
3
-
-
0035936861
-
Automated Solid Phase Synthesis of Oligosaccharides
-
Plante, O. J.; Palmacci, E. R.; Seeberger, P. H. Automated Solid Phase Synthesis of Oligosaccharides Science 2001, 291, 1523-1527 10.1126/science.1057324
-
(2001)
Science
, vol.291
, pp. 1523-1527
-
-
Plante, O.J.1
Palmacci, E.R.2
Seeberger, P.H.3
-
5
-
-
84920194283
-
Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
-
Vitaku, E.; Smith, E. T.; Njardarson, J. T. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals J. Med. Chem. 2014, 57, 10257-10274 10.1021/jm501100b
-
(2014)
J. Med. Chem.
, vol.57
, pp. 10257-10274
-
-
Vitaku, E.1
Smith, E.T.2
Njardarson, J.T.3
-
6
-
-
34249828956
-
A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki-Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks
-
Gillis, E. P.; Burke, M. D. A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki-Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks J. Am. Chem. Soc. 2007, 129, 6716-6717 10.1021/ja0716204
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 6716-6717
-
-
Gillis, E.P.1
Burke, M.D.2
-
7
-
-
40149088849
-
Simple, Efficient, and Modular Syntheses of Polyene Natural Products via Iterative Cross-Coupling
-
Lee, S. J.; Gray, K. C.; Paek, J. S.; Burke, M. D. Simple, Efficient, and Modular Syntheses of Polyene Natural Products via Iterative Cross-Coupling J. Am. Chem. Soc. 2008, 130, 466-468 10.1021/ja078129x
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 466-468
-
-
Lee, S.J.1
Gray, K.C.2
Paek, J.S.3
Burke, M.D.4
-
8
-
-
77952561793
-
Stereoretentive Suzuki-Miyaura Coupling of Haloallenes Enables Fully Stereocontrolled Access to (-)-Peridinin
-
Woerly, E. M.; Cherney, A. H.; Davis, E. K.; Burke, M. D. Stereoretentive Suzuki-Miyaura Coupling of Haloallenes Enables Fully Stereocontrolled Access to (-)-Peridinin J. Am. Chem. Soc. 2010, 132, 6941-6943 10.1021/ja102721p
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 6941-6943
-
-
Woerly, E.M.1
Cherney, A.H.2
Davis, E.K.3
Burke, M.D.4
-
9
-
-
70450207521
-
Iterative Cross-Coupling with MIDA Boronates: Towards a General Strategy for Small Molecule Synthesis
-
Gillis, E. P.; Burke, M. D. Iterative Cross-Coupling with MIDA Boronates: Towards a General Strategy for Small Molecule Synthesis Aldrichimica Acta 2009, 42, 17-27
-
(2009)
Aldrichimica Acta
, vol.42
, pp. 17-27
-
-
Gillis, E.P.1
Burke, M.D.2
-
10
-
-
54849403713
-
Multistep Synthesis of Complex Boronic Acids from Simple MIDA Boronates
-
Gillis, E. P.; Burke, M. D. Multistep Synthesis of Complex Boronic Acids from Simple MIDA Boronates J. Am. Chem. Soc. 2008, 130, 14084-14085 10.1021/ja8063759
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 14084-14085
-
-
Gillis, E.P.1
Burke, M.D.2
-
11
-
-
70349897220
-
Controlled Iterative Cross-Coupling: On the Way to the Automation of Organic Synthesis
-
see: Wang, C.; Glorius, F. Controlled Iterative Cross-Coupling: On the Way to the Automation of Organic Synthesis Angew. Chem., Int. Ed. 2009, 48, 5240-5244 10.1002/anie.200901680
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 5240-5244
-
-
Wang, C.1
Glorius, F.2
-
12
-
-
0000723539
-
Synthesis of Sequence Specific Phenylacetylene Oligomers on an Insoluble Solid Support
-
Young, J. K.; Nelson, J. C.; Moore, J. S. Synthesis of Sequence Specific Phenylacetylene Oligomers on an Insoluble Solid Support J. Am. Chem. Soc. 1994, 116, 10841-10842 10.1021/ja00102a082
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 10841-10842
-
-
Young, J.K.1
Nelson, J.C.2
Moore, J.S.3
-
13
-
-
33846588529
-
-
Noguchi, H.; Hojo, K.; Suginome, M. J. Am. Chem. Soc. 2007, 129, 758-759 10.1021/ja067975p
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 758-759
-
-
Noguchi, H.1
Hojo, K.2
Suginome, M.3
-
14
-
-
0028405746
-
Iterative Divergent/Convergent Approach to Conjugate Oligomers by a Doubling of Molecular Length at Each Iteration. A Rapid Route to Potential Molecular Wire
-
Pearson, D. L.; Schumm, J. S.; Tour, J. M. Iterative Divergent/Convergent Approach to Conjugate Oligomers by a Doubling of Molecular Length at Each Iteration. A Rapid Route to Potential Molecular Wire Macromolecules 1994, 27, 2348-2350 10.1021/ma00086a062
-
(1994)
Macromolecules
, vol.27
, pp. 2348-2350
-
-
Pearson, D.L.1
Schumm, J.S.2
Tour, J.M.3
-
15
-
-
77952410120
-
B-Protected Haloboronic Acids for Iterative Cross-Coupling
-
Ballmer, S. G.; Gillis, E. P.; Burke, M. D. B-Protected Haloboronic Acids for Iterative Cross-Coupling Org. Synth. 2009, 86, 344-359 10.15227/orgsyn.086.0344
-
(2009)
Org. Synth.
, vol.86
, pp. 344-359
-
-
Ballmer, S.G.1
Gillis, E.P.2
Burke, M.D.3
-
16
-
-
77952340967
-
General Method for Synthesis of 2-Heterocyclic N-Methyliminodiacetic Acid Boronates
-
Dick, G. R.; Knapp, D. M.; Gillis, E. P.; Burke, M. D. General Method for Synthesis of 2-Heterocyclic N-Methyliminodiacetic Acid Boronates Org. Lett. 2010, 12, 2314-2317 10.1021/ol100671v
-
(2010)
Org. Lett.
, vol.12
, pp. 2314-2317
-
-
Dick, G.R.1
Knapp, D.M.2
Gillis, E.P.3
Burke, M.D.4
-
17
-
-
78650664109
-
The Slow-Release Strategy in Suzuki-Miyaura Coupling
-
Lennox, A. J. J.; Lloyd-Jones, G. C. The Slow-Release Strategy in Suzuki-Miyaura Coupling Isr. J. Chem. 2010, 50, 664-674 10.1002/ijch.201000074
-
(2010)
Isr. J. Chem.
, vol.50
, pp. 664-674
-
-
Lennox, A.J.J.1
Lloyd-Jones, G.C.2
-
18
-
-
70149117010
-
A General Solution for Unstable Boronic Acids: Slow-Release Cross-Coupling from Air-Stable MIDA Boronates
-
Knapp, D. M.; Gillis, E. P.; Burke, M. D. A General Solution for Unstable Boronic Acids: Slow-Release Cross-Coupling from Air-Stable MIDA Boronates J. Am. Chem. Soc. 2009, 131, 6961-6963 10.1021/ja901416p
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 6961-6963
-
-
Knapp, D.M.1
Gillis, E.P.2
Burke, M.D.3
-
19
-
-
77954846356
-
-
Butters, M.; Harvey, J. N.; Alastair, J. J.; Lloyd-Jones, G. C.; Murray, P. M. Angew. Chem., Int. Ed. 2010, 49, 5156-5160 10.1002/anie.201001522
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 5156-5160
-
-
Butters, M.1
Harvey, J.N.2
Alastair, J.J.3
Lloyd-Jones, G.C.4
Murray, P.M.5
-
20
-
-
37049078584
-
First Total Synthesis of (±)-Peridinin, (+)-Pyrrhoxanthin and the Optically Active Peridinin
-
Yamano, Y.; Ito, M. First Total Synthesis of (±)-Peridinin, (+)-Pyrrhoxanthin and the Optically Active Peridinin J. Chem. Soc., Perkin Trans. 1 1993, 1599-1610 10.1039/p19930001599
-
(1993)
J. Chem. Soc., Perkin Trans. 1
, pp. 1599-1610
-
-
Yamano, Y.1
Ito, M.2
-
21
-
-
0037087785
-
Highly Efficient Stereocontrolled Total Synthesis of the Polyfunctional Carotenoid Peridinin
-
Furuichi, N.; Hara, H.; Osaki, T.; Mori, H.; Katsumura Highly Efficient Stereocontrolled Total Synthesis of the Polyfunctional Carotenoid Peridinin Angew. Chem., Int. Ed. 2002, 41, 1023-1026 10.1002/1521-3773(20020315)41:6<1023::AID-ANIE1023>3.0.CO;2-A
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 1023-1026
-
-
Furuichi, N.1
Hara, H.2
Osaki, T.3
Mori, H.4
Katsumura5
-
22
-
-
8644283571
-
Stereocontrolled Total Synthesis of a Polyfunctional Carotenoid, Peridinin
-
Furuichi, N.; Hara, H.; Osaki, T.; Nakano, M.; Mori, H.; Katsumura Stereocontrolled Total Synthesis of a Polyfunctional Carotenoid, Peridinin J. Org. Chem. 2004, 69, 7949-7959 10.1021/jo048852v
-
(2004)
J. Org. Chem.
, vol.69
, pp. 7949-7959
-
-
Furuichi, N.1
Hara, H.2
Osaki, T.3
Nakano, M.4
Mori, H.5
Katsumura6
-
23
-
-
33746314617
-
Total Synthesis of the Light-Harvesting Carotenoid Peridinin
-
Olpp, T.; Brückner, R. Total Synthesis of the Light-Harvesting Carotenoid Peridinin Angew. Chem., Int. Ed. 2006, 45, 4023-4027 10.1002/anie.200600502
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 4023-4027
-
-
Olpp, T.1
Brückner, R.2
-
24
-
-
33846676191
-
Total Synthesis of Peridinin and Related C37-Norcarotenoid Butenolides
-
Vaz, B.; Domínguez, M.; Alvarez, R.; de Lera, A. R. Total Synthesis of Peridinin and Related C37-Norcarotenoid Butenolides Chem.-Eur. J. 2007, 13, 1273-1290 10.1002/chem.200600959
-
(2007)
Chem. - Eur. J.
, vol.13
, pp. 1273-1290
-
-
Vaz, B.1
Domínguez, M.2
Alvarez, R.3
De Lera, A.R.4
-
25
-
-
84901381097
-
Synthesis of Most Polyene Natural Product Motifs Using Just Twelve Building Blocks and One Coupling Reaction
-
Woerly, E. M.; Roy, J.; Burke, M. D. Synthesis of Most Polyene Natural Product Motifs Using Just Twelve Building Blocks and One Coupling Reaction Nat. Chem. 2014, 6, 484-491 10.1038/nchem.1947
-
(2014)
Nat. Chem.
, vol.6
, pp. 484-491
-
-
Woerly, E.M.1
Roy, J.2
Burke, M.D.3
-
26
-
-
0017197353
-
Single Ionic Channels Induced in Lipid Bilayers by Polyene Antibiotics Amphotericin B and Nystatine
-
Ermishkin, L. N.; Kasumov, K. M.; Potzeluyev, V. M. Single Ionic Channels Induced in Lipid Bilayers by Polyene Antibiotics Amphotericin B and Nystatine Nature 1976, 262, 698-699 10.1038/262698a0
-
(1976)
Nature
, vol.262
, pp. 698-699
-
-
Ermishkin, L.N.1
Kasumov, K.M.2
Potzeluyev, V.M.3
-
27
-
-
0024468204
-
Treatment of Systemic Fungal Infections With Liposomal Amphotericin B
-
Lopez-Berestein, G.; Bodey, G. P.; Fainstein, V.; Keating, M.; Frankel, L. S.; Zeluff, B.; Gentry, L.; Mehta, K. Treatment of Systemic Fungal Infections With Liposomal Amphotericin B Arch. Intern. Med. 1989, 149, 2533-2536 10.1001/archinte.1989.00390110097022
-
(1989)
Arch. Intern. Med.
, vol.149
, pp. 2533-2536
-
-
Lopez-Berestein, G.1
Bodey, G.P.2
Fainstein, V.3
Keating, M.4
Frankel, L.S.5
Zeluff, B.6
Gentry, L.7
Mehta, K.8
-
28
-
-
17644384475
-
Treatment of Candida Infections with Amphotericin B Lipid Complex
-
Ito, J. I.; Hooshmand-Rad, R. Treatment of Candida Infections with Amphotericin B Lipid Complex Clin. Infect. Dis. 2005, 40, S384-S391 10.1086/429330
-
(2005)
Clin. Infect. Dis.
, vol.40
, pp. S384-S391
-
-
Ito, J.I.1
Hooshmand-Rad, R.2
-
29
-
-
84871502341
-
Hidden Killers: Human Fungal Infections
-
Brown, G. D.; Denning, D. W.; Gow, N. A. R.; Levitz, S. M.; Netea, M. G.; White, T. C. Hidden Killers: Human Fungal Infections Sci. Transl. Med. 2012, 4, 165rv13 10.1126/scitranslmed.3004404
-
(2012)
Sci. Transl. Med.
, vol.4
, pp. 165rv13
-
-
Brown, G.D.1
Denning, D.W.2
Gow, N.A.R.3
Levitz, S.M.4
Netea, M.G.5
White, T.C.6
-
30
-
-
33645354495
-
Nystatin Binding by Protoplasts and a Particulate Fraction of Neurospora Crassa, and a Basis for the Selective Toxicity of Polyene Antifungal Antibiotics
-
Kinsky, S. C. Nystatin Binding by Protoplasts and a Particulate Fraction of Neurospora Crassa, and a Basis for the Selective Toxicity of Polyene Antifungal Antibiotics Proc. Natl. Acad. Sci. U. S. A. 1962, 48, 1049-1056 10.1073/pnas.48.6.1049
-
(1962)
Proc. Natl. Acad. Sci. U. S. A.
, vol.48
, pp. 1049-1056
-
-
Kinsky, S.C.1
-
31
-
-
0005151173
-
The Lytic Effect of Polyene Antifungal Antibiotics on Mammalian Erythrocytes
-
Kinsky, S. C.; Avruch, J.; Permutt, M.; Rogers, H. B.; Schonder, A. A. The Lytic Effect of Polyene Antifungal Antibiotics on Mammalian Erythrocytes Biochem. Biophys. Res. Commun. 1962, 9, 503-507 10.1016/0006-291X(62)90116-X
-
(1962)
Biochem. Biophys. Res. Commun.
, vol.9
, pp. 503-507
-
-
Kinsky, S.C.1
Avruch, J.2
Permutt, M.3
Rogers, H.B.4
Schonder, A.A.5
-
32
-
-
50549218374
-
Action of Amphotericin B on Mycoplasma Laidlawii
-
Feingold, D. S. Action of Amphotericin B on Mycoplasma Laidlawii Biochem. Biophys. Res. Commun. 1965, 19, 261-267 10.1016/0006-291X(65)90515-2
-
(1965)
Biochem. Biophys. Res. Commun.
, vol.19
, pp. 261-267
-
-
Feingold, D.S.1
-
33
-
-
36148980794
-
A Post-PKS Oxidation of the Amphotericin B Skeleton Predicted to be Critical for Channel Formation is Not Required for Potent Antifungal Activity
-
Palacios, D. S.; Anderson, T. M.; Burke, M. D. A Post-PKS Oxidation of the Amphotericin B Skeleton Predicted to be Critical for Channel Formation is Not Required for Potent Antifungal Activity J. Am. Chem. Soc. 2007, 129, 13804-13805 10.1021/ja075739o
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 13804-13805
-
-
Palacios, D.S.1
Anderson, T.M.2
Burke, M.D.3
-
34
-
-
79955563191
-
Synthesis-Enabled Functional Group Deletions Reveal Key Underpinnings of Amphotericin B Ion Channel and Antifungal Activities
-
Palacios, D. S.; Dailey, I.; Siebert, D. M.; Wilcock, B. C.; Burke, M. D. Synthesis-Enabled Functional Group Deletions Reveal Key Underpinnings of Amphotericin B Ion Channel and Antifungal Activities Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 6733-6738 10.1073/pnas.1015023108
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 6733-6738
-
-
Palacios, D.S.1
Dailey, I.2
Siebert, D.M.3
Wilcock, B.C.4
Burke, M.D.5
-
35
-
-
0036678492
-
Multiple Functions of Sterols in Yeast Endocytosis
-
Heese-Peck, A.; Pichler, H.; Zanolari, B.; Watanabe, R.; Daum, G.; Riezman, H. Multiple Functions of Sterols in Yeast Endocytosis Mol. Biol. Cell 2002, 13, 2664-2680 10.1091/mbc.E02-04-0186
-
(2002)
Mol. Biol. Cell
, vol.13
, pp. 2664-2680
-
-
Heese-Peck, A.1
Pichler, H.2
Zanolari, B.3
Watanabe, R.4
Daum, G.5
Riezman, H.6
-
36
-
-
40849120821
-
Ergosterol Promotes Pheromone Signaling and Plasma Membrane Fusion in Mating Yeast
-
Jin, H.; McCaffery, J. M.; Grote, E. Ergosterol Promotes Pheromone Signaling and Plasma Membrane Fusion in Mating Yeast J. Cell Biol. 2008, 180, 813-826 10.1083/jcb.200705076
-
(2008)
J. Cell Biol.
, vol.180
, pp. 813-826
-
-
Jin, H.1
McCaffery, J.M.2
Grote, E.3
-
37
-
-
0018152154
-
Effect of Amphotericin B on Cholesterol-Containing Liposomes of Egg Phosphatidylcholine and Didocosenoyl Phosphatidylcholine: A Refinement of the Model for the Formation of Pores by Amphotericin B in Membranes
-
Van Hoogevest, P.; De Kruijff, B. Effect of Amphotericin B on Cholesterol-Containing Liposomes of Egg Phosphatidylcholine and Didocosenoyl Phosphatidylcholine: A Refinement of the Model for the Formation of Pores by Amphotericin B in Membranes Biochim. Biophys. Acta, Biomembr. 1978, 511, 397-407 10.1016/0005-2736(78)90276-6
-
(1978)
Biochim. Biophys. Acta, Biomembr.
, vol.511
, pp. 397-407
-
-
Van Hoogevest, P.1
De Kruijff, B.2
-
38
-
-
84857134391
-
Amphotericin Primarily Kills Yeast by Simply Binding Ergosterol
-
Gray, K. C.; Palacios, D. S.; Dailey, I.; Endo, M. M.; Uno, B. E.; Wilcock, B. C.; Burke, M. D. Amphotericin Primarily Kills Yeast by Simply Binding Ergosterol Proc. Natl. Acad. Sci. U. S. A. 2012, 109, 2234-2239 10.1073/pnas.1117280109
-
(2012)
Proc. Natl. Acad. Sci. U. S. A.
, vol.109
, pp. 2234-2239
-
-
Gray, K.C.1
Palacios, D.S.2
Dailey, I.3
Endo, M.M.4
Uno, B.E.5
Wilcock, B.C.6
Burke, M.D.7
-
39
-
-
84899493685
-
Amphotericin Forms an Extramembranous and Fungicidal Sterol Sponge
-
Anderson, T. M.; Clay, M. C.; Cioffi, A. G.; Diaz, K. A.; Hisao, G. S.; Tuttle, M. D.; Nieuwkoop, A. J.; Comellas, G.; Wang, S.; Uno, B. E.; Wildeman, E. L.; Maryum, N.; Gonen, T.; Rienstra, C. M.; Burke, M. D. Amphotericin Forms an Extramembranous and Fungicidal Sterol Sponge Nat. Chem. Biol. 2014, 10, 400-406 10.1038/nchembio.1496
-
(2014)
Nat. Chem. Biol.
, vol.10
, pp. 400-406
-
-
Anderson, T.M.1
Clay, M.C.2
Cioffi, A.G.3
Diaz, K.A.4
Hisao, G.S.5
Tuttle, M.D.6
Nieuwkoop, A.J.7
Comellas, G.8
Wang, S.9
Uno, B.E.10
Wildeman, E.L.11
Maryum, N.12
Gonen, T.13
Rienstra, C.M.14
Burke, M.D.15
-
40
-
-
67650665790
-
Synthesis and Biological Studies of 35-Deoxy Amphotericin B Methyl Ester
-
Szpilman, A. M.; Cereghetti, D. M.; Manthorpe, J. M.; Wurtz, N. R.; Carreira, E. M. Synthesis and Biological Studies of 35-Deoxy Amphotericin B Methyl Ester Chem.-Eur. J. 2009, 15, 7117-7128 10.1002/chem.200900231
-
(2009)
Chem. - Eur. J.
, vol.15
, pp. 7117-7128
-
-
Szpilman, A.M.1
Cereghetti, D.M.2
Manthorpe, J.M.3
Wurtz, N.R.4
Carreira, E.M.5
-
41
-
-
84878899238
-
C2′-OH of Amphotericin B Plays an Important Role in Binding the Primary Sterol of Human Cells but Not Yeast Cells
-
Wilcock, B. C.; Endo, M. M.; Uno, B. E.; Burke, M. D. C2′-OH of Amphotericin B Plays an Important Role in Binding the Primary Sterol of Human Cells but Not Yeast Cells J. Am. Chem. Soc. 2013, 135, 8488-8491 10.1021/ja403255s
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 8488-8491
-
-
Wilcock, B.C.1
Endo, M.M.2
Uno, B.E.3
Burke, M.D.4
-
42
-
-
84931572030
-
Non-Toxic Antimicrobials that Evade Drug Resistance
-
Davis, S. A.; Vincent, B. M.; Endo, M. M.; Whitesell, L.; Marchillo, K.; Andes, D. R.; Lindquist, S.; Burke, M. D. Non-Toxic Antimicrobials that Evade Drug Resistance Nat. Chem. Biol. 2015, 11, 481 10.1038/nchembio.1821
-
(2015)
Nat. Chem. Biol.
, vol.11
, pp. 481
-
-
Davis, S.A.1
Vincent, B.M.2
Endo, M.M.3
Whitesell, L.4
Marchillo, K.5
Andes, D.R.6
Lindquist, S.7
Burke, M.D.8
-
43
-
-
84896759510
-
Total Synthesis of the Antibiotic Elansolid B1
-
Weber, A.; Dehn, R.; Schläger, N.; Dieter, B.; Kirschning, A. Total Synthesis of the Antibiotic Elansolid B1 Org. Lett. 2014, 16, 568-571 10.1021/ol403441c
-
(2014)
Org. Lett.
, vol.16
, pp. 568-571
-
-
Weber, A.1
Dehn, R.2
Schläger, N.3
Dieter, B.4
Kirschning, A.5
-
44
-
-
84863848886
-
Concise Total Synthesis of (-)-Myxalamide A
-
Fujita, K.; Matsui, R.; Suzuki, T.; Kobayashi, S. Concise Total Synthesis of (-)-Myxalamide A Angew. Chem., Int. Ed. 2012, 51, 7271-7274 10.1002/anie.201203093
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 7271-7274
-
-
Fujita, K.1
Matsui, R.2
Suzuki, T.3
Kobayashi, S.4
-
45
-
-
79551683783
-
Synthesis of Methyl (5Z,8Z,10E,12E,14Z)-Eicosapentaenoate
-
Mohamed, Y. M. A.; Hansen, T. V. Synthesis of Methyl (5Z,8Z,10E,12E,14Z)-Eicosapentaenoate Tetrahedron Lett. 2011, 52, 1057-1059 10.1016/j.tetlet.2010.12.078
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 1057-1059
-
-
Mohamed, Y.M.A.1
Hansen, T.V.2
-
46
-
-
84872687745
-
Extending the Utility of the Bartoli Indolization: Synthesis of Marinoquinolines C and E
-
Lindsay, A. C.; Sperry, J. Extending the Utility of the Bartoli Indolization: Synthesis of Marinoquinolines C and E Synlett 2013, 24, 461-464 10.1055/s-0032-1318137
-
(2013)
Synlett
, vol.24
, pp. 461-464
-
-
Lindsay, A.C.1
Sperry, J.2
-
47
-
-
79958831683
-
One-Pot Reductive Amination and Suzuki-Miyaura Cross-Coupling of Formyl Aryl and Heteroaryl MIDA Boronates in Array Format
-
Grob, J. E.; Nunez, J.; Dechantsreiter, M. A.; Hamann, L. G. One-Pot Reductive Amination and Suzuki-Miyaura Cross-Coupling of Formyl Aryl and Heteroaryl MIDA Boronates in Array Format J. Org. Chem. 2011, 76, 4930-4940 10.1021/jo2005928
-
(2011)
J. Org. Chem.
, vol.76
, pp. 4930-4940
-
-
Grob, J.E.1
Nunez, J.2
Dechantsreiter, M.A.3
Hamann, L.G.4
-
48
-
-
84055193795
-
Regioselective Synthesis and Slow-Release Suzuki-Miyaura Cross-Coupling of MIDA Boronate-Functionalized Isoxazoles and Triazoles
-
Grob, J. E.; Nunez, J.; Dechantsreiter, M. A.; Hamann, L. G. Regioselective Synthesis and Slow-Release Suzuki-Miyaura Cross-Coupling of MIDA Boronate-Functionalized Isoxazoles and Triazoles J. Org. Chem. 2011, 76, 10241-10248 10.1021/jo201973t
-
(2011)
J. Org. Chem.
, vol.76
, pp. 10241-10248
-
-
Grob, J.E.1
Nunez, J.2
Dechantsreiter, M.A.3
Hamann, L.G.4
-
49
-
-
84868379221
-
One-Pot C-N/C-C Cross-Coupling of Methyliminodiacetic Acid Boronyl Arenes Enabled by Protective Enolization
-
Grob, J. E.; Dechantsreiter, M. A.; Tichkule, R. B.; Connolly, M. K.; Honda, A.; Tomlinson, R. C.; Hamann, L. G. One-Pot C-N/C-C Cross-Coupling of Methyliminodiacetic Acid Boronyl Arenes Enabled by Protective Enolization Org. Lett. 2012, 14, 5578-5581 10.1021/ol302702q
-
(2012)
Org. Lett.
, vol.14
, pp. 5578-5581
-
-
Grob, J.E.1
Dechantsreiter, M.A.2
Tichkule, R.B.3
Connolly, M.K.4
Honda, A.5
Tomlinson, R.C.6
Hamann, L.G.7
-
50
-
-
84868105815
-
Quaterpyridine Ligands for Panchromatic Ru(II) Dye Sensitizers
-
Coluccini, C.; Manfredi, N.; Salamone, M. M.; Ruffo, R.; Lobello, M. G.; Angelis, F. D.; Abbotto, A. Quaterpyridine Ligands for Panchromatic Ru(II) Dye Sensitizers J. Org. Chem. 2012, 77, 7945-7956 10.1021/jo301226z
-
(2012)
J. Org. Chem.
, vol.77
, pp. 7945-7956
-
-
Coluccini, C.1
Manfredi, N.2
Salamone, M.M.3
Ruffo, R.4
Lobello, M.G.5
Angelis, F.D.6
Abbotto, A.7
-
51
-
-
84908099389
-
Lithiation-Borylation Methodology and Its Application in Synthesis
-
Leonori, D.; Aggarwal, V. K. Lithiation-Borylation Methodology and Its Application in Synthesis Acc. Chem. Res. 2014, 47, 3174-3183 10.1021/ar5002473
-
(2014)
Acc. Chem. Res.
, vol.47
, pp. 3174-3183
-
-
Leonori, D.1
Aggarwal, V.K.2
-
52
-
-
84865850287
-
Catalytic Enantioselective Synthesis of Secondary Alkylboronate Building Blocks With and Without Metals
-
Bull, J. A. Catalytic Enantioselective Synthesis of Secondary Alkylboronate Building Blocks With and Without Metals Angew. Chem., Int. Ed. 2012, 51, 8930-8932 10.1002/anie.201203876
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 8930-8932
-
-
Bull, J.A.1
-
53
-
-
77953268734
-
Synthesis of Enantiomerically Pure Oxiranylboronic Esters
-
Fernandez, E.; Frey, W.; Pietruszka, J. Synthesis of Enantiomerically Pure Oxiranylboronic Esters Synlett 2010, 2010 (9) 1386-1388 10.1055/s-0029-1219829
-
(2010)
Synlett
, vol.2010
, Issue.9
, pp. 1386-1388
-
-
Fernandez, E.1
Frey, W.2
Pietruszka, J.3
-
54
-
-
80955126099
-
Diastereoselective Aziridination of 2-B(pin)-Substituted Allylic Alcohols: An Efficient Approach to Novel Organoboron Compounds
-
Hernandez-Toribo, J.; Hussain, M. M.; Cheng, K.; Carroll, P. J.; Walsh, P. J. Diastereoselective Aziridination of 2-B(pin)-Substituted Allylic Alcohols: An Efficient Approach to Novel Organoboron Compounds Org. Lett. 2011, 13, 6094-6097 10.1021/ol202588g
-
(2011)
Org. Lett.
, vol.13
, pp. 6094-6097
-
-
Hernandez-Toribo, J.1
Hussain, M.M.2
Cheng, K.3
Carroll, P.J.4
Walsh, P.J.5
-
55
-
-
80052305738
-
Pinene-Derived Iminodiacetic Acid (PIDA): A Powerful Ligand for Stereoselective Synthesis and Iterative Cross-Coupling of C(sp3) Boronate Building Blocks
-
Li, J.; Burke, M. D. Pinene-Derived Iminodiacetic Acid (PIDA): A Powerful Ligand for Stereoselective Synthesis and Iterative Cross-Coupling of C(sp3) Boronate Building Blocks J. Am. Chem. Soc. 2011, 133, 13774-13777 10.1021/ja205912y
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13774-13777
-
-
Li, J.1
Burke, M.D.2
-
56
-
-
84923106899
-
Synergistic Interplay of a Non-Heme Iron Catalyst and Amino Acid Coligands in H2O2 Activation for Asymmetric Epoxidation of α-Alkyl-Substituted Styrenes
-
Cussó, O.; Ribas, X.; Lloret-Fillol; Costas, M. Synergistic Interplay of a Non-Heme Iron Catalyst and Amino Acid Coligands in H2O2 Activation for Asymmetric Epoxidation of α-Alkyl-Substituted Styrenes Angew. Chem., Int. Ed. 2015, 54, 2729-2733 10.1002/anie.201410557
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 2729-2733
-
-
Cussó, O.1
Ribas, X.2
Lloret-Fillol3
Costas, M.4
-
57
-
-
58049195806
-
Asymmetric Epoxidation of 1,1-Disubstituted Terminal Olefins by Chiral Dioxirane via a Planar-like Transition State
-
Wang, B.; Wong, A.; Zhao, M.-X.; Shi, Y. Asymmetric Epoxidation of 1,1-Disubstituted Terminal Olefins by Chiral Dioxirane via a Planar-like Transition State J. Org. Chem. 2008, 73, 9539-9543 10.1021/jo801576k
-
(2008)
J. Org. Chem.
, vol.73
, pp. 9539-9543
-
-
Wang, B.1
Wong, A.2
Zhao, M.-X.3
Shi, Y.4
-
58
-
-
61849149861
-
Asymmetric Hydroboration of 1,1-Disubstituted Alkenes
-
Thomas, S. P.; Aggarwal, V. K. Asymmetric Hydroboration of 1,1-Disubstituted Alkenes Angew. Chem., Int. Ed. 2009, 48, 1896-1898 10.1002/anie.200805604
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 1896-1898
-
-
Thomas, S.P.1
Aggarwal, V.K.2
-
59
-
-
80052332176
-
Amphoteric α-boryl aldehydes
-
He, Z.; Yudin, A. K. Amphoteric α-boryl aldehydes J. Am. Chem. Soc. 2011, 133, 13770-13773 10.1021/ja205910d
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13770-13773
-
-
He, Z.1
Yudin, A.K.2
-
60
-
-
84922740518
-
1,2-Boryl Migration Empowers Regiodivergent Synthesis of Borylated Furans
-
Shiroodi, R. K.; Koleda, O.; Gevorgyan, V. 1,2-Boryl Migration Empowers Regiodivergent Synthesis of Borylated Furans J. Am. Chem. Soc. 2014, 136, 13146-13149 10.1021/ja507054j
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 13146-13149
-
-
Shiroodi, R.K.1
Koleda, O.2
Gevorgyan, V.3
-
61
-
-
84867774444
-
Oxidative Geminal Functionalization of Organoboron Compounds
-
He, Z.; Trinchera, P.; Adahi, S.; St. Denis, J. D.; Yudin, A. K. Oxidative Geminal Functionalization of Organoboron Compounds Angew. Chem., Int. Ed. 2012, 51, 11092-11096 10.1002/anie.201206501
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 11092-11096
-
-
He, Z.1
Trinchera, P.2
Adahi, S.3
St. Denis, J.D.4
Yudin, A.K.5
-
62
-
-
84882246299
-
α-Boryl Isocyanides Enable Facile Preparation of Bioactive Boropeptides
-
Zajdlik, A.; Wang, Z.; Hickey, J. L.; Aman, A.; Schimmer, A. D.; Yudin, A. K. α-Boryl Isocyanides Enable Facile Preparation of Bioactive Boropeptides Angew. Chem., Int. Ed. 2013, 52, 8411-8415 10.1002/anie.201302818
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 8411-8415
-
-
Zajdlik, A.1
Wang, Z.2
Hickey, J.L.3
Aman, A.4
Schimmer, A.D.5
Yudin, A.K.6
-
63
-
-
84919363201
-
Boron-Containing Enamine and Enamide Linchpins in the Synthesis of Nitrogen Heterocycles
-
St. Denis, J. D.; Zajdlik, A.; Tan, J.; Trinchera, P.; Lee, C. F.; He, Z.; Adachi, S.; Yudin, A. K. Boron-Containing Enamine and Enamide Linchpins in the Synthesis of Nitrogen Heterocycles J. Am. Chem. Soc. 2014, 136, 17669-17673 10.1021/ja510963k
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 17669-17673
-
-
St. Denis, J.D.1
Zajdlik, A.2
Tan, J.3
Trinchera, P.4
Lee, C.F.5
He, Z.6
Adachi, S.7
Yudin, A.K.8
-
64
-
-
67749113467
-
Cross Coupling Reactions of Chiral Secondary Organoboronic Esters With Retention of Configuration
-
Imao, D.; Glasspoole, B. W.; Laberge, V. S.; Crudden, C. M. Cross Coupling Reactions of Chiral Secondary Organoboronic Esters With Retention of Configuration J. Am. Chem. Soc. 2009, 131, 5024-5025 10.1021/ja8094075
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5024-5025
-
-
Imao, D.1
Glasspoole, B.W.2
Laberge, V.S.3
Crudden, C.M.4
-
65
-
-
84921044400
-
Stereospecific Couplings of Secondary and Tertiary Boronic Esters
-
Leonori, D.; Aggarwal, V. K. Stereospecific Couplings of Secondary and Tertiary Boronic Esters Angew. Chem., Int. Ed. 2015, 54, 1082-1096 10.1002/anie.201407701
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 1082-1096
-
-
Leonori, D.1
Aggarwal, V.K.2
-
66
-
-
79952656192
-
Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-Organometallics as Reaction Partners
-
Jana, R.; Pathak, T. P.; Sigman, M. S. Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-Organometallics as Reaction Partners Chem. Rev. 2011, 111, 1417-1492 10.1021/cr100327p
-
(2011)
Chem. Rev.
, vol.111
, pp. 1417-1492
-
-
Jana, R.1
Pathak, T.P.2
Sigman, M.S.3
-
67
-
-
84907943523
-
Stereospecific Pd-Catalyzed Cross-Coupling Reactions of Secondary Alkylboron Nucleophiles and Aryl Chlorides
-
Li, L.; Zhao, S.; Joshi-Pangu, A.; Diane, M.; Biscoe, M. R. Stereospecific Pd-Catalyzed Cross-Coupling Reactions of Secondary Alkylboron Nucleophiles and Aryl Chlorides J. Am. Chem. Soc. 2014, 136, 14027-14030 10.1021/ja508815w
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 14027-14030
-
-
Li, L.1
Zhao, S.2
Joshi-Pangu, A.3
Diane, M.4
Biscoe, M.R.5
-
68
-
-
84867366948
-
Stereospecific Cross-Coupling of Secondary Organotrifluoroborates: Potassium 1-(Benzyloxy)alkyltrifluoroborates
-
Molander, G. A.; Wisniewski, S. R. Stereospecific Cross-Coupling of Secondary Organotrifluoroborates: Potassium 1-(Benzyloxy)alkyltrifluoroborates J. Am. Chem. Soc. 2012, 134, 16856 10.1021/ja307861n
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 16856
-
-
Molander, G.A.1
Wisniewski, S.R.2
-
69
-
-
77957126089
-
Stereospecific Suzuki- Miyaura Coupling of Chiral α-(Acylamino)benzylboronic Esters with Inversion of Configuration
-
Ohmura, T.; Awano, T.; Suginome, M. Stereospecific Suzuki- Miyaura Coupling of Chiral α-(Acylamino)benzylboronic Esters with Inversion of Configuration J. Am. Chem. Soc. 2010, 132, 13191-13193 10.1021/ja106632j
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 13191-13193
-
-
Ohmura, T.1
Awano, T.2
Suginome, M.3
-
70
-
-
78650163175
-
Stereospecific Cross-Coupling of Secondary Alkyl β-Trifluoroboratoamides
-
Sandrock, D. L.; Jean-Gérard, L.; Chen, C.-Y.; Dreher, S. D.; Molander, G. A. Stereospecific Cross-Coupling of Secondary Alkyl β-Trifluoroboratoamides J. Am. Chem. Soc. 2010, 132, 17108-17110 10.1021/ja108949w
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 17108-17110
-
-
Sandrock, D.L.1
Jean-Gérard, L.2
Chen, C.-Y.3
Dreher, S.D.4
Molander, G.A.5
-
71
-
-
84924787758
-
Synthesis of Many Different Types of Organic Small Molecules Using One Automated Process
-
Li, J.; Ballmer, S. G.; Gillis, E. P.; Fujii, S.; Schmidt, M. J.; Palazzolo, A. M. E.; Lehmann, J. W.; Morehouse, G. F.; Burke, M. D. Synthesis of Many Different Types of Organic Small Molecules Using One Automated Process Science 2015, 347, 1221-1226 10.1126/science.aaa5414
-
(2015)
Science
, vol.347
, pp. 1221-1226
-
-
Li, J.1
Ballmer, S.G.2
Gillis, E.P.3
Fujii, S.4
Schmidt, M.J.5
Palazzolo, A.M.E.6
Lehmann, J.W.7
Morehouse, G.F.8
Burke, M.D.9
-
72
-
-
0001014077
-
Daphniphyllum Alkaloids. 12. A Proposed Biosynthesis of the Pentacyclic Skeleton. Proto-Daphniphylline
-
Heathcock, C. H.; Piettre, S.; Ruggeri, R. B.; Ragan, J. A.; Kath, J. C. Daphniphyllum Alkaloids. 12. A Proposed Biosynthesis of the Pentacyclic Skeleton. Proto-Daphniphylline J. Org. Chem. 1992, 57, 2554-2566 10.1021/jo00035a009
-
(1992)
J. Org. Chem.
, vol.57
, pp. 2554-2566
-
-
Heathcock, C.H.1
Piettre, S.2
Ruggeri, R.B.3
Ragan, J.A.4
Kath, J.C.5
-
73
-
-
84883258908
-
A Remote-Controlled Adaptive Medchem Lab: An Innovative Approach to Enable Drug Discovery in the 21st Century
-
Godfrey, A. G.; Masquelin, T.; Hemmerle, H. A Remote-Controlled Adaptive Medchem Lab: An Innovative Approach to Enable Drug Discovery in the 21st Century Drug Discovery Today 2013, 18, 795-802 10.1016/j.drudis.2013.03.001
-
(2013)
Drug Discovery Today
, vol.18
, pp. 795-802
-
-
Godfrey, A.G.1
Masquelin, T.2
Hemmerle, H.3
-
74
-
-
84899920463
-
Accelerating Spirocyclic Polyketide Synthesis using Flow Chemistry
-
Newton, S.; Carter, C. F.; Pearson, C. M.; Alves, L. de C.; Lange, H.; Thansandote, P.; Ley, S. V. Accelerating Spirocyclic Polyketide Synthesis using Flow Chemistry Angew. Chem., Int. Ed. 2014, 53, 4915-4920 10.1002/anie.201402056
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 4915-4920
-
-
Newton, S.1
Carter, C.F.2
Pearson, C.M.3
Alves, L.D.C.4
Lange, H.5
Thansandote, P.6
Ley, S.V.7
-
75
-
-
84884651413
-
Efficient Synthesis of Natural Products Aided by Automated Synthesizers and Microreactors
-
Pignataro, B. Wiley-VCH: Weinheim, Germany
-
Fuse, S.; Machida, K.; Takahashi, T. Efficient Synthesis of Natural Products Aided by Automated Synthesizers and Microreactors. In New Strategies in Chemical Synthesis and Catalysis; Pignataro, B., Ed.; Wiley-VCH: Weinheim, Germany, 2012; pp 33-57.
-
(2012)
New Strategies in Chemical Synthesis and Catalysis
, pp. 33-57
-
-
Fuse, S.1
Machida, K.2
Takahashi, T.3
-
76
-
-
85027955443
-
March of the Machines
-
Ley, S. V.; Fitzpatrick, D. E.; Ingham, R. J.; Myers, R. M. March of the Machines Angew. Chem., Int. Ed. 2015, 54, 3449-3464 10.1002/anie.201410744
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 3449-3464
-
-
Ley, S.V.1
Fitzpatrick, D.E.2
Ingham, R.J.3
Myers, R.M.4
-
77
-
-
0041811829
-
Total Synthesis of Both Enantiomers of the Macrocyclic Lactone Citreofuran
-
Bracher, F.; Schulte, B. Total Synthesis of Both Enantiomers of the Macrocyclic Lactone Citreofuran Nat. Prod. Res. 2003, 17, 293-299 10.1080/1478641031000137004
-
(2003)
Nat. Prod. Res.
, vol.17
, pp. 293-299
-
-
Bracher, F.1
Schulte, B.2
-
78
-
-
0029081685
-
A Short Synthesis of Natural (-)-Oblongolide via an Intramolecular or a Transannular Diels-Alder Reaction
-
Shing, T. K. M.; Yang, J. A Short Synthesis of Natural (-)-Oblongolide via an Intramolecular or a Transannular Diels-Alder Reaction J. Org. Chem. 1995, 60, 5785-5789 10.1021/jo00123a011
-
(1995)
J. Org. Chem.
, vol.60
, pp. 5785-5789
-
-
Shing, T.K.M.1
Yang, J.2
-
79
-
-
23944490138
-
Enantioselective Organocatalytic Intramolecular Diels-Alder Reactions. The Asymmetric Synthesis of Solanapyrone D
-
Wilson, R. M.; Jen, W. S.; MacMillan, D. W. C. Enantioselective Organocatalytic Intramolecular Diels-Alder Reactions. The Asymmetric Synthesis of Solanapyrone D J. Am. Chem. Soc. 2005, 127, 11616-11617 10.1021/ja054008q
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 11616-11617
-
-
Wilson, R.M.1
Jen, W.S.2
MacMillan, D.W.C.3
-
80
-
-
77954244311
-
A Two-Step Mimic for Direct, Asymmetric Bromonium- and Chloronium-Induced Polyene Cyclizations
-
Snyder, S. A.; Treitler, D. S.; Schall, A. A Two-Step Mimic for Direct, Asymmetric Bromonium- and Chloronium-Induced Polyene Cyclizations Tetrahedron 2010, 66, 4796-4804 10.1016/j.tet.2010.03.037
-
(2010)
Tetrahedron
, vol.66
, pp. 4796-4804
-
-
Snyder, S.A.1
Treitler, D.S.2
Schall, A.3
|