-
1
-
-
79955006138
-
Molecular mechanisms of antibiotic resistance
-
Wright, G. D. Molecular mechanisms of antibiotic resistance Chem. Commun. 2011, 47, 4055-4061
-
(2011)
Chem. Commun.
, vol.47
, pp. 4055-4061
-
-
Wright, G.D.1
-
2
-
-
0034999522
-
Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in the United States during 1999-2000, including a comparison of resistance rates since 1994-1995
-
Doern, G. V.; Heilmann, K. P.; Huynh, H. K.; Rhomberg, P. R.; Coffman, S. L.; Brueggemann, A. B. Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in the United States during 1999-2000, including a comparison of resistance rates since 1994-1995 Antimicrob. Agents Chemother. 2001, 45, 1721-1729
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 1721-1729
-
-
Doern, G.V.1
Heilmann, K.P.2
Huynh, H.K.3
Rhomberg, P.R.4
Coffman, S.L.5
Brueggemann, A.B.6
-
3
-
-
0012473679
-
Ketolides: Novel antibacterial agents designed to overcome resistance to erythromycin A within gram-positive cocci
-
Schonfeld, W. Kirst, H. A. Verlag: Basel
-
Bryskier, A.; Denis, A. Ketolides: Novel antibacterial agents designed to overcome resistance to erythromycin A within gram-positive cocci. In Macrolide Antibiotics; Schonfeld, W.; Kirst, H. A., Eds.; Verlag: Basel, 2002; pp 97-140.
-
(2002)
Macrolide Antibiotics
, pp. 97-140
-
-
Bryskier, A.1
Denis, A.2
-
4
-
-
78651493389
-
Desmethyl macrolides: Synthesis and evaluation of 4,8,10-tridesmethyl telithromycin
-
Velvadapu, V.; Paul, T.; Wagh, B.; Klepacki, D.; Guvench, O.; MacKerell, A., Jr.; Andrade, R. B. Desmethyl macrolides: Synthesis and evaluation of 4,8,10-tridesmethyl telithromycin ACS Med. Chem. Lett. 2010, 2, 68-72
-
(2010)
ACS Med. Chem. Lett.
, vol.2
, pp. 68-72
-
-
Velvadapu, V.1
Paul, T.2
Wagh, B.3
Klepacki, D.4
Guvench, O.5
Mackerell Jr., A.6
Andrade, R.B.7
-
5
-
-
80052697933
-
Total synthesis of (-)-4,8,10-tridesmethyl telithromycin
-
Velvadapu, V.; Paul, T.; Wagh, B.; Glassford, I.; DeBrosse, C.; Andrade, R. B. Total synthesis of (-)-4,8,10-tridesmethyl telithromycin J. Org. Chem. 2011, 76, 7516-7527
-
(2011)
J. Org. Chem.
, vol.76
, pp. 7516-7527
-
-
Velvadapu, V.1
Paul, T.2
Wagh, B.3
Glassford, I.4
Debrosse, C.5
Andrade, R.B.6
-
6
-
-
84863267800
-
Desmethyl macrolides: Synthesis and evaluation of 4,10-didesmethyl telithromycin
-
Velvadapu, V.; Glassford, I.; Lee, M.; Paul, T.; DeBrosse, C.; Klepacki, D.; Small, M.; C.; MacKerell, A. D., Jr.; Andrade, R. B. Desmethyl macrolides: synthesis and evaluation of 4,10-didesmethyl telithromycin ACS Med. Chem. Lett. 2012, 3, 211-215
-
(2012)
ACS Med. Chem. Lett.
, vol.3
, pp. 211-215
-
-
Velvadapu, V.1
Glassford, I.2
Lee, M.3
Paul, T.4
Debrosse, C.5
Klepacki, D.6
Small, M.C.7
Mackerell Jr., A.D.8
Andrade, R.B.9
-
7
-
-
0029745623
-
Throwing a spanner in the works: Antibiotics and the translation apparatus
-
Spahn, C. M.; Prescott, C. D. Throwing a spanner in the works: antibiotics and the translation apparatus J. Mol. Med. 1996, 74, 423-439
-
(1996)
J. Mol. Med.
, vol.74
, pp. 423-439
-
-
Spahn, C.M.1
Prescott, C.D.2
-
8
-
-
70349859708
-
Modeling a Macrocyclic bis[spirodiepoxide] strategy to erythronolide A
-
Ghosh, P.; Zhang, Y.; Emge, T. J.; Williams, L. J. Modeling a Macrocyclic bis[spirodiepoxide] strategy to erythronolide A Org. Lett. 2009, 11, 4402-4405
-
(2009)
Org. Lett.
, vol.11
, pp. 4402-4405
-
-
Ghosh, P.1
Zhang, Y.2
Emge, T.J.3
Williams, L.J.4
-
9
-
-
80053062591
-
Direct entry to erythronolides via a cyclic bis[allene]
-
Liu, K.; Kim, H.; Ghosh, P.; Akhmedov, N. G.; Williams, L. J. Direct entry to erythronolides via a cyclic bis[allene] J. Am. Chem. Soc. 2011, 133, 14968-14971
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 14968-14971
-
-
Liu, K.1
Kim, H.2
Ghosh, P.3
Akhmedov, N.G.4
Williams, L.J.5
-
10
-
-
78449303571
-
A de novo approach to the synthesis of glycosylated methymycin analogues with structural and stereochemical diversity
-
For a contrasting and elegant approach to macrolide analogues wherein the carbohydrate moiety has been modified while maintaining the aglycone intact, see Borisova, S. A.; Guppi, S. R.; Kim, H. J.; Wu, B.; Penn, J. H.; Liu, H.-W.; O'Doherty, G. A. A de novo approach to the synthesis of glycosylated methymycin analogues with structural and stereochemical diversity Org. Lett. 2010, 12, 5150
-
(2010)
Org. Lett.
, vol.12
, pp. 5150
-
-
Borisova, S.A.1
Guppi, S.R.2
Kim, H.J.3
Wu, B.4
Penn, J.H.5
Liu, H.-W.6
O'Doherty, G.A.7
-
11
-
-
55049123651
-
Macrolide myths
-
references therein
-
Mankin, A. S. Macrolide myths Curr. Opin. Microbiol. 2008, 11, 414-421 and references therein
-
(2008)
Curr. Opin. Microbiol.
, vol.11
, pp. 414-421
-
-
Mankin, A.S.1
-
12
-
-
17444421169
-
BK antibiotics bound to mutated large ribosomal subunits provide a structural explanation for resistance
-
BK antibiotics bound to mutated large ribosomal subunits provide a structural explanation for resistance Cell 2005, 121, 257-270
-
(2005)
Cell
, vol.121
, pp. 257-270
-
-
Tu, D.1
Blaha, G.2
Moore, P.B.3
Steitz, T.A.4
-
13
-
-
0029878720
-
VMD: Visual Molecular Dynamics
-
Humphrey, W.; Dalke, A.; Schulten, K. VMD: Visual Molecular Dynamics J. Mol. Graph. 1996, 14, 33-38
-
(1996)
J. Mol. Graph.
, vol.14
, pp. 33-38
-
-
Humphrey, W.1
Dalke, A.2
Schulten, K.3
-
14
-
-
0001994881
-
Susceptibility testing of antimicrobials in liquid media
-
4 th ed. Lorain, V. Williams & Wilkins: Baltimore
-
Amsterdam, D. Susceptibility testing of antimicrobials in liquid media. In Antibiotics in Laboratory Medicine, 4 th ed.; Lorain, V., Ed.; Williams & Wilkins: Baltimore, 1996; pp 52-111.
-
(1996)
Antibiotics in Laboratory Medicine
, pp. 52-111
-
-
Amsterdam, D.1
-
15
-
-
0033598258
-
Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2- ylidene ligands
-
Scholl, M.; Ding, S.; Lee, C. W.; Grubbs, R. H. Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands Org. Lett. 1999, 1, 953-956
-
(1999)
Org. Lett.
, vol.1
, pp. 953-956
-
-
Scholl, M.1
Ding, S.2
Lee, C.W.3
Grubbs, R.H.4
-
16
-
-
0037486826
-
Carbon-carbon bond formations involving organochromium (III) reagents
-
For a review, see Furstner, A. Carbon-carbon bond formations involving organochromium (III) reagents Chem. Rev. 1999, 99, 991-1045
-
(1999)
Chem. Rev.
, vol.99
, pp. 991-1045
-
-
Furstner, A.1
-
17
-
-
33845922132
-
-
For a similar approach using this tactic
-
For a similar approach using this tactic: Venkatraman, L.; Salomon, C. E.; Sherman, D. E.; Fecik, R. A. J. Org. Chem. 2006, 71, 9853
-
(2006)
J. Org. Chem.
, vol.71
, pp. 9853
-
-
Venkatraman, L.1
Salomon, C.E.2
Sherman, D.E.3
Fecik, R.A.4
-
18
-
-
34249058524
-
Total synthesis of erythromycin B
-
Breton, P.; Hergenrother, P. J.; Hida, T.; Hodgson, A.; Kraynack, E.; Kym, P.; Lee, W.-C.; Loft, M.; Judd, A.; Yamashita, M.; Martin, S. F. Total synthesis of erythromycin B Tetrahedron 2007, 63, 5709
-
(2007)
Tetrahedron
, vol.63
, pp. 5709
-
-
Breton, P.1
Hergenrother, P.J.2
Hida, T.3
Hodgson, A.4
Kraynack, E.5
Kym, P.6
Lee, W.-C.7
Loft, M.8
Judd, A.9
Yamashita, M.10
Martin, S.F.11
-
19
-
-
0001436716
-
Manipulation of modular polyketide synthases
-
Katz, L. Manipulation of modular polyketide synthases Chem. Rev. 1997, 97, 2557-2575
-
(1997)
Chem. Rev.
, vol.97
, pp. 2557-2575
-
-
Katz, L.1
-
20
-
-
34547135676
-
Stereoselective formal total synthesis of (+)-methynolide
-
Yadav, J. S.; Pratap, T. V.; Rajender, V. Stereoselective formal total synthesis of (+)-methynolide J. Org. Chem. 2007, 72, 5882-5885
-
(2007)
J. Org. Chem.
, vol.72
, pp. 5882-5885
-
-
Yadav, J.S.1
Pratap, T.V.2
Rajender, V.3
-
21
-
-
0040746033
-
Palladium- and molybdenum-catalyzed hydrostannation of alkynes. A novel access to regio- and stereodefined vinylstannanes
-
Zhang, H. X.; Guibe, F.; Balavoine, G. Palladium- and molybdenum-catalyzed hydrostannation of alkynes. A novel access to regio- and stereodefined vinylstannanes J. Org. Chem. 1990, 55, 1857-1867
-
(1990)
J. Org. Chem.
, vol.55
, pp. 1857-1867
-
-
Zhang, H.X.1
Guibe, F.2
Balavoine, G.3
-
22
-
-
0012016624
-
Enantioselective aldol condensations. 2. Erythro -selective chiral aldol condensations via boron enolates
-
Evans, D. A.; Bartroli, J.; Shih, T. L. Enantioselective aldol condensations. 2. Erythro -selective chiral aldol condensations via boron enolates J. Am. Chem. Soc. 1981, 103, 2127-2109
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 2127-2109
-
-
Evans, D.A.1
Bartroli, J.2
Shih, T.L.3
-
23
-
-
0019440449
-
Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin
-
Woodward, R. B. Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin J. Am. Chem. Soc. 1981, 103, 3215-3217
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 3215-3217
-
-
Woodward, R.B.1
-
24
-
-
37049034657
-
Concise syntheses of D-desosamine, 2-thiopyrimidinyl desosamine donors and methyl desosaminide analogues from D-glucose
-
Velvadapu, V.; Andrade, R. B. Concise syntheses of D-desosamine, 2-thiopyrimidinyl desosamine donors and methyl desosaminide analogues from D-glucose Carbohydr. Res. 2008, 343, 145-150
-
(2008)
Carbohydr. Res.
, vol.343
, pp. 145-150
-
-
Velvadapu, V.1
Andrade, R.B.2
-
25
-
-
0023901653
-
Modification of macrolide antibiotics. Synthesis of 11-deoxy-11- (carboxyamino)-6- O -methylerythromycin A-11,12-(cyclic esters) via an intramolecular Michael reaction of O -carbamates with an α,β- unsaturated ketone
-
Baker, W. R.; Clark, J. D.; Stephens, R. L.; Kim, K. H. Modification of macrolide antibiotics. Synthesis of 11-deoxy-11-(carboxyamino)-6- O -methylerythromycin A-11,12-(cyclic esters) via an intramolecular Michael reaction of O -carbamates with an α,β-unsaturated ketone J. Org. Chem. 1988, 53, 2340-2345
-
(1988)
J. Org. Chem.
, vol.53
, pp. 2340-2345
-
-
Baker, W.R.1
Clark, J.D.2
Stephens, R.L.3
Kim, K.H.4
-
26
-
-
85172055154
-
Preparation of macrolide 9-Alkyl- and 9-Alkylidenyl-6- O -Alkyl-11,12-carbamate ketolide clarithromycin derivatives as anti-bacterial agents
-
May 4
-
Grant, E. B., III. Preparation of macrolide 9-Alkyl- and 9-Alkylidenyl-6- O -Alkyl-11,12-carbamate ketolide clarithromycin derivatives as anti-bacterial agents. WO 2006047167 A2, May 4, 2006.
-
(2006)
WO 2006047167 A2
-
-
Grant III, E.B.1
-
27
-
-
0001409192
-
Tris(dimethylamino)sulfonium difluorotrimethylsilicate, a mild reagent for the removal of silicon protecting groups
-
Scheidt, K. A.; Chen, H.; Follows, B. C.; Chemler, S. R.; Coffey, D. S.; Roush, W. R. Tris(dimethylamino)sulfonium difluorotrimethylsilicate, a mild reagent for the removal of silicon protecting groups J. Org. Chem. 1998, 63, 6436-6437
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6436-6437
-
-
Scheidt, K.A.1
Chen, H.2
Follows, B.C.3
Chemler, S.R.4
Coffey, D.S.5
Roush, W.R.6
-
28
-
-
0000466427
-
New and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compounds
-
Corey, E. J.; Kim, C. U. New and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compounds J. Am. Chem. Soc. 1972, 94, 7586-7587
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 7586-7587
-
-
Corey, E.J.1
Kim, C.U.2
-
29
-
-
0035950132
-
Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria
-
Schlunzen, F.; Zarivach, R.; Harms, J.; Bashan, A.; Tocilj, A.; Albrecht, R.; Yonath, A. Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria Nature 2001, 413, 814-821
-
(2001)
Nature
, vol.413
, pp. 814-821
-
-
Schlunzen, F.1
Zarivach, R.2
Harms, J.3
Bashan, A.4
Tocilj, A.5
Albrecht, R.6
Yonath, A.7
-
30
-
-
78049302075
-
Structures of the Escherichia coli ribosome with antibiotics bound near the peptidyl transferase center explain spectra of drug action
-
Dunkle, J. A.; Xiong, L.; Mankin, A. S.; Cate, J. H. D. Structures of the Escherichia coli ribosome with antibiotics bound near the peptidyl transferase center explain spectra of drug action Proc. Natl. Acad. Sci. U.S.A. 2010, 107, 17152-17157
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 17152-17157
-
-
Dunkle, J.A.1
Xiong, L.2
Mankin, A.S.3
Cate, J.H.D.4
-
31
-
-
0037433589
-
2D Conformationally sampled pharmacophore: A ligand-based pharmacophore to differentiate delta opioid agonists from antagonists
-
Bernard, D.; Coop, A.; MacKerell, A. D., Jr. 2D Conformationally sampled pharmacophore: a ligand-based pharmacophore to differentiate delta opioid agonists from antagonists J. Am. Chem. Soc. 2003, 125, 3103-3107
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3103-3107
-
-
Bernard, D.1
Coop, A.2
Mackerell Jr., A.D.3
|