Year |
Citation |
Score |
2007 |
Denmark SE, Wilson TW, Burk MT, Heemstra JR. Enantioselective construction of quaternary stereogenic carbons by the Lewis base catalyzed additions of silyl ketene imines to aldehydes. Journal of the American Chemical Society. 129: 14864-5. PMID 17988135 DOI: 10.1021/Ja077134Y |
0.648 |
|
2007 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids: catalytic, enantioselective vinylogous aldol addition reactions. The Journal of Organic Chemistry. 72: 5668-88. PMID 17583959 DOI: 10.1021/Jo070638U |
0.601 |
|
2006 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids. Vinylogous aldol addition reactions of conjugated N,O-silyl ketene acetals to aldehydes. Journal of the American Chemical Society. 128: 1038-9. PMID 16433495 DOI: 10.1021/Ja056747C |
0.602 |
|
2005 |
Denmark SE, Heemstra JR, Beutner GL. Catalytic, enantioselective, vinylogous aldol reactions. Angewandte Chemie (International Ed. in English). 44: 4682-98. PMID 15940727 DOI: 10.1002/Anie.200462338 |
0.595 |
|
2005 |
Denmark SE, Heemstra JR, Beutner GL. Katalytische enantioselektive vinyloge Aldolreaktionen Angewandte Chemie. 117: 4760-4777. DOI: 10.1002/Ange.200462338 |
0.547 |
|
2004 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids: Vinylogous aldol additions of silyl dienol ethers to aldehydes Synlett. 2411-2416. DOI: 10.1055/S-2004-834789 |
0.651 |
|
2003 |
Denmark SE, Heemstra JR. Lewis base activation of Lewis acids. Catalytic enantioselective addition of silyl enol ethers of achiral methyl ketones to aldehydes. Organic Letters. 5: 2303-6. PMID 12816434 DOI: 10.1021/Ol034641L |
0.635 |
|
Low-probability matches (unlikely to be authored by this person) |
2009 |
Heemstra JR, Walsh CT, Sattely ES. Enzymatic tailoring of ornithine in the biosynthesis of the Rhizobium cyclic trihydroxamate siderophore vicibactin. Journal of the American Chemical Society. 131: 15317-29. PMID 19778043 DOI: 10.1021/Ja9056008 |
0.255 |
|
2014 |
Setser JW, Heemstra JR, Walsh CT, Drennan CL. Crystallographic evidence of drastic conformational changes in the active site of a flavin-dependent N-hydroxylase. Biochemistry. 53: 6063-77. PMID 25184411 DOI: 10.1021/Bi500655Q |
0.197 |
|
2011 |
Jiang W, Heemstra JR, Forseth RR, Neumann CS, Manaviazar S, Schroeder FC, Hale KJ, Walsh CT. Biosynthetic chlorination of the piperazate residue in kutzneride biosynthesis by KthP. Biochemistry. 50: 6063-72. PMID 21648411 DOI: 10.1021/Bi200656K |
0.187 |
|
2008 |
Heemstra JR, Walsh CT. Tandem action of the O2- and FADH2-dependent halogenases KtzQ and KtzR produce 6,7-dichlorotryptophan for kutzneride assembly. Journal of the American Chemical Society. 130: 14024-5. PMID 18828589 DOI: 10.1021/Ja806467A |
0.136 |
|
2015 |
Ruffner DE, Schmidt EW, Heemstra JR. Assessing the combinatorial potential of the RiPP cyanobactin tru pathway. Acs Synthetic Biology. 4: 482-92. PMID 25140729 DOI: 10.1021/Sb500267D |
0.126 |
|
2012 |
Neumann CS, Jiang W, Heemstra JR, Gontang EA, Kolter R, Walsh CT. Biosynthesis of piperazic acid via N5-hydroxy-ornithine in Kutzneria spp. 744. Chembiochem : a European Journal of Chemical Biology. 13: 972-6. PMID 22522643 DOI: 10.1002/Cbic.201200054 |
0.108 |
|
2010 |
Zhang W, Heemstra JR, Walsh CT, Imker HJ. Activation of the pacidamycin PacL adenylation domain by MbtH-like proteins. Biochemistry. 49: 9946-7. PMID 20964365 DOI: 10.1021/Bi101539B |
0.067 |
|
2016 |
Tianero MD, Pierce E, Raghuraman S, Sardar D, McIntosh JA, Heemstra JR, Schonrock Z, Covington BC, Maschek JA, Cox JE, Bachmann BO, Olivera BM, Ruffner DE, Schmidt EW. Metabolic model for diversity-generating biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. PMID 26831074 DOI: 10.1073/Pnas.1525438113 |
0.06 |
|
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