Year |
Citation |
Score |
2018 |
Kato H, Kai A, Kawabata T, Sunderhaus JD, McAfoos TJ, Finefield JM, Sugimoto Y, Williams RM, Tsukamoto S. Corrigendum to "Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts" [Bioorg. Med. Chem. Lett. 27 (22) (2017) 4975-4978]. Bioorganic & Medicinal Chemistry Letters. PMID 29903661 DOI: 10.1016/J.Bmcl.2018.06.013 |
0.714 |
|
2017 |
Kato H, Kai A, Kawabata T, Sunderhaus JD, McAfoos TJ, Finefield JM, Sugimoto Y, Williams RM, Tsukamoto S. Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts. Bioorganic & Medicinal Chemistry Letters. PMID 29037945 DOI: 10.1016/J.Bmcl.2017.10.017 |
0.727 |
|
2015 |
Kato H, Nakahara T, Yamaguchi M, Kagiyama I, Finefield JM, Sunderhaus JD, Sherman DH, Williams RM, Tsukamoto S. Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp. Tetrahedron Letters. 56: 247-251. PMID 25767298 DOI: 10.1016/J.Tetlet.2014.11.083 |
0.568 |
|
2014 |
Kato H, Nakamura Y, Finefield JM, Umaoka H, Nakahara T, Williams RM, Tsukamoto S. Corrigendum to "study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide e and 6-hydroxydeoxybrevianamide E" [Tetrahedron Lett. 52 (2011) 6923-6926] Tetrahedron Letters. 55: 559-560. DOI: 10.1016/J.Tetlet.2013.11.076 |
0.42 |
|
2013 |
Sunderhaus JD, McAfoos TJ, Finefield JM, Kato H, Li S, Tsukamoto S, Sherman DH, Williams RM. Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide B. Organic Letters. 15: 22-5. PMID 23249380 DOI: 10.1021/Ol302901P |
0.723 |
|
2013 |
Finefield JM, Williams RM. Correction to Synthesis of Notoamide J: A Potentially Pivotal Intermediate in the Biosynthesis of Several Prenylated Indole Alkaloids The Journal of Organic Chemistry. 78: 8214-8214. DOI: 10.1021/Jo401209S |
0.551 |
|
2012 |
Li S, Anand K, Tran H, Yu F, Finefield JM, Sunderhaus JD, McAfoos TJ, Tsukamoto S, Williams RM, Sherman DH. Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(-)-notoamide, paraherquamide and malbrancheamide pathways. Medchemcomm. 3: 987-996. PMID 23213353 DOI: 10.1039/C2Md20029E |
0.735 |
|
2012 |
Finefield JM, Sherman DH, Kreitman M, Williams RM. Enantiomeric natural products: occurrence and biogenesis. Angewandte Chemie (International Ed. in English). 51: 4802-36. PMID 22555867 DOI: 10.1002/Anie.201107204 |
0.482 |
|
2012 |
Finefield JM, Frisvad JC, Sherman DH, Williams RM. Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids. Journal of Natural Products. 75: 812-33. PMID 22502590 DOI: 10.1021/Np200954V |
0.536 |
|
2012 |
Li S, Finefield JM, Sunderhaus JD, McAfoos TJ, Williams RM, Sherman DH. Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloids. Journal of the American Chemical Society. 134: 788-91. PMID 22188465 DOI: 10.1021/Ja2093212 |
0.741 |
|
2012 |
Li S, Finefield JM, Sunderhaus JD, McAfoos TJ, Williams RM, Sherman DH. Correction to “Biochemical Characterization of NotB as an FAD-Dependent Oxidase in the Biosynthesis of Notoamide Indole Alkaloids” Journal of the American Chemical Society. 134: 20565-20565. DOI: 10.1021/Ja3107753 |
0.72 |
|
2012 |
Finefield JM, Sherman DH, Kreitman M, Williams RM. Enantiomere Naturstoffe: Vorkommen und Biogenese Angewandte Chemie. 124: 4886-4920. DOI: 10.1002/Ange.201107204 |
0.457 |
|
2011 |
Kato H, Nakamura Y, Finefield JM, Umaoka H, Nakahara T, Williams RM, Tsukamoto S. Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E. Tetrahedron Letters. 52: 6923-6926. PMID 22140281 DOI: 10.1016/J.Tetlet.2011.10.065 |
0.497 |
|
2011 |
Finefield JM, Greshock TJ, Sherman DH, Tsukamoto S, Williams RM. Notoamide E: Biosynthetic incorporation into notoamides C and D in cultures of Aspergillus versicolor NRRL 35600. Tetrahedron Letters. 52: 1987-1989. PMID 22140279 DOI: 10.1016/J.Tetlet.2011.02.078 |
0.514 |
|
2011 |
Finefield JM, Kato H, Greshock TJ, Sherman DH, Tsukamoto S, Williams RM. Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide. Organic Letters. 13: 3802-5. PMID 21714564 DOI: 10.1021/Ol201284Y |
0.528 |
|
2011 |
Finefield JM, Sherman DH, Tsukamoto S, Williams RM. Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J. The Journal of Organic Chemistry. 76: 5954-8. PMID 21504234 DOI: 10.1021/Jo200218A |
0.573 |
|
2010 |
Ding Y, de Wet JR, Cavalcoli J, Li S, Greshock TJ, Miller KA, Finefield JM, Sunderhaus JD, McAfoos TJ, Tsukamoto S, Williams RM, Sherman DH. Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp. Journal of the American Chemical Society. 132: 12733-40. PMID 20722388 DOI: 10.1021/Ja1049302 |
0.718 |
|
2010 |
Finefield JM, Williams RM. Synthesis of notoamide J: a potentially pivotal intermediate in the biosynthesis of several prenylated indole alkaloids. The Journal of Organic Chemistry. 75: 2785-9. PMID 20359229 DOI: 10.1021/Jo100332C |
0.545 |
|
2009 |
Li Z, Shalitin D, Finefield J, Leung C, Hu M, Shen J, Li M, Wang CS, Steinberg JA, Sanchez E, Chen H, Williams RM, Bonavida B, Berenson JR. Multiple Myeloma-Specific Targeted Therapy: Use of the Tumor Specific Immunoglobulin Gene Sequence to Activate Drugs Only within Tumor Cells. Blood. 114: 1851-1851. DOI: 10.1182/Blood.V114.22.1851.1851 |
0.423 |
|
2008 |
Ding Y, Gruschow S, Greshock TJ, Finefield JM, Sherman DH, Williams RM. Detection of VM55599 and preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: biosynthetic implications. Journal of Natural Products. 71: 1574-8. PMID 18754595 DOI: 10.1021/Np800292N |
0.461 |
|
2006 |
Hoover TR, Groeper JA, Parrott RW, Chandrashekar SP, Finefield JM, Dominguez A, Hitchcock SR. Towards the development of oxadiazinanones as chiral auxiliaries: synthesis and application of N3-haloacetyloxadiazinanones Tetrahedron Asymmetry. 17: 1831-1841. DOI: 10.1016/J.Tetasy.2006.06.036 |
0.321 |
|
2004 |
Hitchcock SR, Casper DM, Vaughn JF, Finefield JM, Ferrence GM, Esken JM. Intramolecular chiral relay at stereogenic nitrogen. Synthesis and application of a new chiral auxiliary derived from (1R,2S)-norephedrine and acetone. The Journal of Organic Chemistry. 69: 714-8. PMID 14750795 DOI: 10.1021/Jo035325N |
0.337 |
|
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