| Year |
Citation |
Score |
| 2018 |
Vagstad AL, Kuranaga T, Püntener S, Pattabiraman VR, Bode JW, Piel J. Introduction of D-Amino Acids in Minimalistic Peptide Substrates by an S-Adenosyl-L-Methionine Radical Epimerase. Angewandte Chemie (International Ed. in English). PMID 30521081 DOI: 10.1002/Anie.201809508 |
0.411 |
|
| 2016 |
Liu SM, Mazunin D, Pattabiraman VR, Bode JW. Synthesis of Bifunctional Potassium Acyltrifluoroborates. Organic Letters. PMID 27709962 DOI: 10.1021/Acs.Orglett.6B02652 |
0.383 |
|
| 2014 |
Wucherpfennig TG, Pattabiraman VR, Limberg FRP, Ruiz-Rodríguez J, Bode JW. Traceless preparation of C-terminal α-Ketoacids for chemical protein synthesis by α-Ketoacid-hydroxylamine ligation: Synthesis of SUMO2/3 Angewandte Chemie - International Edition. 53: 12248-12252. PMID 25244549 DOI: 10.1002/Anie.201407014 |
0.3 |
|
| 2014 |
Wucherpfennig TG, Rohrbacher F, Pattabiraman VR, Bode JW. Formation and rearrangement of homoserine depsipeptides and depsiproteins in the α-ketoacid-hydroxylamine ligation with 5-oxaproline Angewandte Chemie - International Edition. 53: 12244-12247. PMID 25243600 DOI: 10.1002/Anie.201406097 |
0.349 |
|
| 2011 |
Pattabiraman VR, Bode JW. Rethinking amide bond synthesis Nature. 480: 471-479. PMID 22193101 DOI: 10.1038/Nature10702 |
0.422 |
|
| 2010 |
Ross AC, Liu H, Pattabiraman VR, Vederas JC. Synthesis of the lantibiotic lactocin S using peptide cyclizations on solid phase. Journal of the American Chemical Society. 132: 462-3. PMID 20017553 DOI: 10.1021/Ja9095945 |
0.673 |
|
| 2009 |
Liu H, Pattabiraman VR, Vederas JC. Synthesis and biological activity of oxa-lacticin A2, a lantibiotic analogue with sulfur replaced by oxygen. Organic Letters. 11: 5574-7. PMID 19921853 DOI: 10.1021/Ol9025205 |
0.681 |
|
| 2008 |
Pattabiraman VR, McKinnie SM, Vederas JC. Solid-supported synthesis and biological evaluation of the lantibiotic peptide bis(desmethyl) lacticin 3147 A2. Angewandte Chemie (International Ed. in English). 47: 9472-5. PMID 18937239 DOI: 10.1002/Anie.200802919 |
0.686 |
|
| 2008 |
Pattabiraman V, McKinnie S, Vederas J. Cover Picture: Solid-Supported Synthesis and Biological Evaluation of the Lantibiotic Peptide Bis(desmethyl) Lacticin 3147 A2 (Angew. Chem. Int. Ed. 49/2008) Angewandte Chemie International Edition. 47: 9357-9357. DOI: 10.1002/Anie.200890251 |
0.676 |
|
| 2008 |
Pattabiraman V, McKinnie S, Vederas J. Titelbild: Solid-Supported Synthesis and Biological Evaluation of the Lantibiotic Peptide Bis(desmethyl) Lacticin 3147 A2 (Angew. Chem. 49/2008) Angewandte Chemie. 120: 9497-9497. DOI: 10.1002/Ange.200890300 |
0.686 |
|
| 2007 |
Liu H, Pattabiraman VR, Vederas JC. Stereoselective syntheses of 4-oxa diaminopimelic acid and its protected derivatives via aziridine ring opening. Organic Letters. 9: 4211-4. PMID 17850092 DOI: 10.1021/Ol701742X |
0.663 |
|
| 2007 |
Pattabiraman VR, Stymiest JL, Derksen DJ, Martin NI, Vederas JC. Multiple on-resin olefin metathesis to form ring-expanded analogues of the lantibiotic peptide, lacticin 3147 A2. Organic Letters. 9: 699-702. PMID 17286377 DOI: 10.1021/Ol063133J |
0.457 |
|
| 2003 |
Pal M, Madan M, Padakanti S, Pattabiraman VR, Kalleda S, Vanguri A, Mullangi R, Mamidi NV, Casturi SR, Malde A, Gopalakrishnan B, Yeleswarapu KR. Synthesis and cyclooxygenase-2 inhibiting property of 1,5-diarylpyrazoles with substituted benzenesulfonamide moiety as pharmacophore: Preparation of sodium salt for injectable formulation. Journal of Medicinal Chemistry. 46: 3975-84. PMID 12954051 DOI: 10.1021/jm020563g |
0.335 |
|
| 2002 |
Padakanti S, Veeramaneni VR, Pattabiraman VR, Pal M, Yeleswarapu KR. A simple and rapid entry to 5-alkyl (aryl)-5-hydroxy-3,4-diarylfuranones and 3a-hydroxy-1-aryl-2,3a,4,5-tetrahydronaphthofuranones via a tandem esterification and oxidative cyclization process Tetrahedron Letters. 43: 8715-8719. DOI: 10.1002/chin.200305115 |
0.375 |
|
| 2002 |
Pattabiraman VR, Padakanti S, Veeramaneni VR, Pal M, Yeleswarapu KR. Synthesis of 3,4-diarylsubstituted maleic anhydride/maleimide via unusual oxidative cyclization of phenacyl ester/amide Synlett. 947-951. |
0.388 |
|
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