Year |
Citation |
Score |
2016 |
Zhang P, Kriegel RM, Frost JW. B–O–B Catalyzed Cycloadditions of Acrylic Acids Acs Sustainable Chemistry & Engineering. 4: 6991-6995. DOI: 10.1021/Acssuschemeng.6B01908 |
0.412 |
|
2016 |
Zhang P, Nguyen V, Frost JW. Synthesis of Terephthalic Acid from Methane Acs Sustainable Chemistry & Engineering. 4: 5998-6001. DOI: 10.1021/Acssuschemeng.6B01268 |
0.468 |
|
2014 |
Miller KK, Zhang P, Nishizawa-Brennen Y, Frost JW. Synthesis of biobased terephthalic acid from cycloaddition of isoprene with acrylic acid Acs Sustainable Chemistry and Engineering. 2: 2053-2056. DOI: 10.1021/Sc5003038 |
0.451 |
|
2007 |
Ran N, Frost JW. Directed evolution of 2-keto-3-deoxy-6-phosphogalactonate aldolase to replace 3-deoxy-D-arabino-heptulosonic acid 7-phosphate synthase. Journal of the American Chemical Society. 129: 6130-9. PMID 17451239 DOI: 10.1021/Ja067330P |
0.495 |
|
2006 |
Xie D, Shao Z, Achkar J, Zha W, Frost JW, Zhao H. Microbial synthesis of triacetic acid lactone. Biotechnology and Bioengineering. 93: 727-36. PMID 16245348 DOI: 10.1002/Bit.20759 |
0.375 |
|
2006 |
Draths KM, Frost JW, Stowers MD. Draths Corp. will produce shikimic acid Industrial Bioprocessing. 28: 1-2. |
0.326 |
|
2005 |
Achkar J, Xian M, Zhao H, Frost JW. Biosynthesis of phloroglucinol. Journal of the American Chemical Society. 127: 5332-3. PMID 15826166 DOI: 10.1021/Ja042340G |
0.33 |
|
2005 |
Li W, Xie D, Frost JW. Benzene-free synthesis of catechol: interfacing microbial and chemical catalysis. Journal of the American Chemical Society. 127: 2874-82. PMID 15740122 DOI: 10.1021/Ja045148N |
0.555 |
|
2004 |
Ran N, Draths KM, Frost JW. Creation of a shikimate pathway variant. Journal of the American Chemical Society. 126: 6856-7. PMID 15174841 DOI: 10.1021/Ja049730N |
0.37 |
|
2004 |
Guo J, Frost JW. Synthesis of aminoshikimic acid. Organic Letters. 6: 1585-8. PMID 15128242 DOI: 10.1021/Ol049666E |
0.682 |
|
2004 |
Zha W, Shao Z, Frost JW, Zhao H. Rational pathway engineering of type I fatty acid synthase allows the biosynthesis of triacetic acid lactone from D-glucose in vivo. Journal of the American Chemical Society. 126: 4534-5. PMID 15070368 DOI: 10.1021/Ja0317271 |
0.47 |
|
2003 |
Niu W, Molefe MN, Frost JW. Microbial synthesis of the energetic material precursor 1,2,4-butanetriol. Journal of the American Chemical Society. 125: 12998-9. PMID 14570452 DOI: 10.1021/Ja036391+ |
0.698 |
|
2003 |
Yi J, Draths KM, Li K, Frost JW. Altered glucose transport and shikimate pathway product yields in E. coli. Biotechnology Progress. 19: 1450-9. PMID 14524706 DOI: 10.1021/Bp0340584 |
0.607 |
|
2003 |
Chandran SS, Yi J, Draths KM, von Daeniken R, Weber W, Frost JW. Phosphoenolpyruvate availability and the biosynthesis of shikimic acid. Biotechnology Progress. 19: 808-14. PMID 12790643 DOI: 10.1021/Bp025769P |
0.722 |
|
2003 |
Chang YC, Almy EA, Blamer GA, Gray JI, Frost JW, Strasburg GM. Antioxidant activity of 3-dehydroshikimic acid in liposomes, emulsions, and bulk oil. Journal of Agricultural and Food Chemistry. 51: 2753-7. PMID 12696968 DOI: 10.1021/Jf025970F |
0.358 |
|
2002 |
Yi J, Li K, Draths KM, Frost JW. Modulation of phosphoenolpyruvate synthase expression increases shikimate pathway product yields in E. coli. Biotechnology Progress. 18: 1141-8. PMID 12467444 DOI: 10.1021/Bp020101W |
0.614 |
|
2002 |
Guo J, Frost JW. Kanosamine biosynthesis: a likely source of the aminoshikimate pathway's nitrogen atom. Journal of the American Chemical Society. 124: 10642-3. PMID 12207504 DOI: 10.1021/Ja026628M |
0.677 |
|
2002 |
Hansen CA, Frost JW. Deoxygenation of polyhydroxybenzenes: an alternative strategy for the benzene-free synthesis of aromatic chemicals. Journal of the American Chemical Society. 124: 5926-7. PMID 12022810 DOI: 10.1021/Ja0176346 |
0.693 |
|
2002 |
Niu W, Draths KM, Frost JW. Benzene-free synthesis of adipic acid. Biotechnology Progress. 18: 201-11. PMID 11934286 DOI: 10.1021/Bp010179X |
0.636 |
|
2002 |
Guo J, Frost JW. Biosynthesis of 1-deoxy-1-imino-D-erythrose 4-phosphate: a defining metabolite in the aminoshikimate pathway. Journal of the American Chemical Society. 124: 528-9. PMID 11804477 DOI: 10.1021/Ja016963V |
0.644 |
|
2001 |
Barker JL, Frost JW. Microbial synthesis of p-hydroxybenzoic acid from glucose. Biotechnology and Bioengineering. 76: 376-90. PMID 11745165 DOI: 10.1002/Bit.10160 |
0.67 |
|
2001 |
Ran N, Knop DR, Draths KM, Frost JW. Benzene-free synthesis of hydroquinone. Journal of the American Chemical Society. 123: 10927-34. PMID 11686696 DOI: 10.1021/Ja016460P |
0.479 |
|
2001 |
Knop DR, Draths KM, Chandran SS, Barker JL, von Daeniken R, Weber W, Frost JW. Hydroaromatic equilibration during biosynthesis of shikimic acid. Journal of the American Chemical Society. 123: 10173-82. PMID 11603966 DOI: 10.1021/Ja0109444 |
0.757 |
|
2001 |
Chandran SS, Frost JW. Aromatic inhibitors of dehydroquinate synthase: synthesis, evaluation and implications for gallic acid biosynthesis. Bioorganic & Medicinal Chemistry Letters. 11: 1493-6. PMID 11412967 DOI: 10.1016/S0960-894X(01)00065-8 |
0.607 |
|
2001 |
Gibson JM, Thomas PS, Thomas JD, Barker JL, Chandran SS, Harrup MK, Draths KM, Frost JW. Benzene-Free Synthesis of Phenol This research was supported by a grant awarded by the U.S. Department of Agriculture. Angewandte Chemie (International Ed. in English). 40: 1945-1948. PMID 11385681 DOI: 10.1002/1521-3773(20010518)40:10<1945::Aid-Anie1945>3.0.Co;2-5 |
0.652 |
|
2001 |
Draths KM, Kambourakis S, Li K, Frost JW. 3-Dehydroshikimic acid: A building block for chemical synthesis from renewable feedstocks Acs Symposium Series. 784: 133-146. |
0.751 |
|
2000 |
Kambourakis S, Frost JW. Synthesis of gallic acid: Cu(2+)-mediated oxidation of 3-dehydroshikimic acid. The Journal of Organic Chemistry. 65: 6904-9. PMID 11031008 DOI: 10.1021/Jo000335Z |
0.763 |
|
2000 |
Kambourakis S, Draths KM, Frost JW. Synthesis of gallic acid and pyrogallol from glucose: Replacing natural product isolation with microbial catalysis [9] Journal of the American Chemical Society. 122: 9042-9043. DOI: 10.1021/Ja000853R |
0.761 |
|
1999 |
Li K, Frost JW. Microbial synthesis of 3-dehydroshikimic acid: a comparative analysis of D-xylose, L-arabinose, and D-glucose carbon sources. Biotechnology Progress. 15: 876-83. PMID 10514257 DOI: 10.1021/Bp990095C |
0.429 |
|
1999 |
Li K, Mikola MR, Draths KM, Worden RM, Frost JW. Fed-batch fermentor synthesis of 3-dehydroshikimic acid using recombinant Escherichia coli. Biotechnology and Bioengineering. 64: 61-73. PMID 10397840 DOI: 10.1002/(Sici)1097-0290(19990705)64:1<61::Aid-Bit7>3.0.Co;2-G |
0.506 |
|
1999 |
Li K, Frost JW. Utilizing succinic acid as glucose adjunct in fed-batch fermentation: Is butane a feedstock option in microbe-catalyzed synthesis? [8] Journal of the American Chemical Society. 121: 9461-9462. DOI: 10.1021/ja992477k |
0.339 |
|
1999 |
Tian F, Migaud ME, Frost JW. myo-Inositol 1-phosphate synthase: Does a single active-site amino acid catalyze multiple proton transfers? Journal of the American Chemical Society. 121: 5795-5796. DOI: 10.1021/Ja9900196 |
0.386 |
|
1999 |
Hansen CA, Dean AB, Draths KM, Frost JW. Synthesis of 1,2,3,4-tetrahydroxybenzene from D-glucose: Exploiting myo- inositol as a precursor to aromatic chemicals [11] Journal of the American Chemical Society. 121: 3799-3800. DOI: 10.1021/Ja9840293 |
0.64 |
|
1999 |
Draths KM, Knop DR, Frost JW. Shikimic acid and quinic acid: Replacing isolation from plant sources with recombinant microbial biocatalysis [4] Journal of the American Chemical Society. 121: 1603-1604. DOI: 10.1021/Ja9830243 |
0.401 |
|
1998 |
Carpenter EP, Hawkins AR, Frost JW, Brown KA. Structure of dehydroquinate synthase reveals an active site capable of multistep catalysis. Nature. 394: 299-302. PMID 9685163 DOI: 10.1038/28431 |
0.301 |
|
1998 |
Li K, Frost JW. Synthesis of vanillin from glucose [2] Journal of the American Chemical Society. 120: 10545-10546. DOI: 10.1021/Ja9817747 |
0.316 |
|
1996 |
Migaud ME, Chee-Sanford JC, Tiedje JM, Frost JW. Benzylfumaric, benzylmaleic, and Z- and E-phenylitaconic acids: synthesis, characterization, and correlation with a metabolite generated by Azoarcus tolulyticus Tol-4 during anaerobic toluene degradation. Applied and Environmental Microbiology. 62: 974-8. PMID 8975624 DOI: 10.1128/Aem.62.3.974-978.1996 |
0.439 |
|
1996 |
Chee-Sanford JC, Frost JW, Fries MR, Zhou J, Tiedje JM. Evidence for acetyl coenzyme A and cinnamoyl coenzyme A in the anaerobic toluene mineralization pathway in Azoarcus tolulyticus Tol-4. Applied and Environmental Microbiology. 62: 964-73. PMID 8975623 DOI: 10.1128/Aem.62.3.964-973.1996 |
0.439 |
|
1996 |
Snell KD, Draths KM, Frost JW. Synthetic modification of the Escherichia coli chromosome: Enhancing the biocatalytic conversion of glucose into aromatic chemicals Journal of the American Chemical Society. 118: 5605-5614. DOI: 10.1021/Ja9538041 |
0.443 |
|
1996 |
Migaud ME, Frost JW. Elaboration of a general strategy for inhibition of myo-inositol 1-phosphate synthase: Active site interactions of analogues possessing oxidized reaction centers Journal of the American Chemical Society. 118: X-500. DOI: 10.1021/Ja952570I |
0.327 |
|
1996 |
Richman JE, Chang YC, Kambourakis S, Draths KM, Almy E, Snell KD, Strasburg GM, Frost JW. Reaction of 3-dehydroshikimic acid with molecular oxygen and hydrogen peroxide: Products, mechanism, and associated antioxidant activity Journal of the American Chemical Society. 118: 11587-11591. DOI: 10.1021/Ja952317I |
0.761 |
|
1995 |
Montchamp JL, Tian F, Frost JW. Double Arbuzov reaction of in situ generated bis(trimethylsiloxy)phosphine with dielectrophiles: Methodology for the synthesis of cyclic phosphinic acids Journal of Organic Chemistry. 60: 6076-6081. DOI: 10.1021/Jo00124A018 |
0.399 |
|
1994 |
Draths KM, Frost JW. Environmentally compatible synthesis of adipic acid from D-glucose [16] Journal of the American Chemical Society. 116: 399-400. |
0.344 |
|
1993 |
Dell KA, Frost JW. Identification and removal of impediments to biocatalytic synthesis of aromatics from D-glucose: Rate-limiting enzymes in the common pathway of aromatic amino acid biosynthesis Journal of the American Chemical Society. 115: 11581-11589. |
0.378 |
|
1992 |
Montchamp JL, Piehler LT, Frost JW. Diastereoselection and in Vivo inhibition of 3-dehydroquinate synthase Journal of the American Chemical Society. 114: 4453-4459. DOI: 10.1021/Ja00038A002 |
0.313 |
|
1992 |
Draths KM, Pompliano DL, Conley DL, Frost JW, Berry A, Disbrow GL, Staversky RJ, Lievense JC. Biocatalytic synthesis of aromatics from D-glucose: The role of transketolase Journal of the American Chemical Society. 114: 3956-3962. DOI: 10.1021/Ja00036A050 |
0.783 |
|
1989 |
Pompliano DL, Reimer LM, Myrvold S, Frost JW. Probing lethal metabolic perturbations in plants with chemical inhibition of dehydroquinate synthase Journal of the American Chemical Society. 111: 1866-1871. DOI: 10.1021/Ja00187A049 |
0.731 |
|
1989 |
Myrvold S, Reimer LM, Pompliano DL, Frost JW. Chemical inhibition of dehydroquinate synthase Journal of the American Chemical Society. 111: 1861-1866. DOI: 10.1021/Ja00187A048 |
0.736 |
|
1987 |
Mehdi S, Frost JW, Knowles JR. Dehydroquinate synthase from Escherichia coli, and its substrate 3-deoxy-D-arabino-heptulosonic acid 7-phosphate. Methods in Enzymology. 142: 306-14. PMID 3037261 DOI: 10.1016/S0076-6879(87)42041-7 |
0.696 |
|
1987 |
Roach MC, Ungar LW, Zare RN, Reimer LM, Pompliano DL, Frost JW. Fluorescence detection of alkylphosphonic acids using p-(9-anthroyloxy)phenacyl bromide [2] Analytical Chemistry. 59: 1056-1059. DOI: 10.1021/Ac00134A027 |
0.746 |
|
1986 |
Reimer LM, Conley DL, Pompliano DL, Frost JW. Construction of an enzyme-targeted organophosphonate using immobilized enzyme and whole cell synthesis Journal of the American Chemical Society. 108: 8010-8015. DOI: 10.1021/Ja00285A022 |
0.741 |
|
1986 |
Cordeiro ML, Pompliano DL, Frost JW. Degradation and detoxification of organophosphonates: Cleavage of the carbon to phosphorus bond Journal of the American Chemical Society. 108: 332-334. |
0.72 |
|
1984 |
Frost JW, Bender JL, Kadonaga JT, Knowles JR. Dehydroquinate synthase from Escherichia coli: purification, cloning, and construction of overproducers of the enzyme. Biochemistry. 23: 4470-5. PMID 6386050 DOI: 10.1021/Bi00314A036 |
0.703 |
|
1984 |
Frost JW, Knowles JR. 3-Deoxy-D-arabino-heptulosonic acid 7-phosphate: chemical synthesis and isolation from Escherichia coli auxotrophs. Biochemistry. 23: 4465-9. PMID 6386049 DOI: 10.1021/Bi00314A035 |
0.695 |
|
1981 |
Frost JW, Rastetter WH. Flavoprotein monooxygenases: A chemical model Journal of the American Chemical Society. 103: 5242-5245. DOI: 10.1021/Ja00407A052 |
0.574 |
|
1981 |
FROST JW, RASTETTER WH. ChemInform Abstract: BIOMIMETIC 8α FUNCTIONALIZATION OF RIBOFLAVIN Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198108331 |
0.571 |
|
1980 |
Frost JW, Rastetter WH. Biomimetic 8.alpha. functionalization of riboflavin Journal of the American Chemical Society. 102: 7157-7159. DOI: 10.1021/Ja00543A069 |
0.558 |
|
1980 |
Frost JW, Rastetter WH. Biomimetic 8α functionalization of riboflavin [32] Journal of the American Chemical Society. 102: 7157-7159. |
0.568 |
|
1979 |
Rastetter WH, Adams J, Frost JW, Nummy LJ, Frommer JE, Roberts KB. On the involvement of lipoic acid in .alpha.-keto acid dehydrogenase complexes Journal of the American Chemical Society. 101: 2752-2753. DOI: 10.1021/Ja00504A055 |
0.684 |
|
1979 |
Rastetter WH, Gadek TR, Tane JP, Frost JW. Oxidations and oxygen transfers effected by a flavin N(5)-oxide. A model for flavin-dependent monooxygenases [22] Journal of the American Chemical Society. 101: 2228-2231. DOI: 10.1021/Ja00502A063 |
0.578 |
|
1979 |
Rastetter WH, Frost JW. Oxaziridines and oxygen transfer. A revised mechanism for the kinetic resolution of 2-n-propyl-3-methyl-3-iso-butyloxaziridine by brucine. Tetrahedron Letters. 20: 3353-3356. DOI: 10.1016/S0040-4039(01)95407-3 |
0.572 |
|
1979 |
Feuer H, Blecker LR, Jans RW, Frost JW. Alkyl nitrate nitration of active methylene compounds nitration of 1-methyl-4-piperidone, 1-methyl-2-pyrrolidinone and 1,3-dimethyl-2-pyrrolidinone (1) Journal of Heterocyclic Chemistry. 16: 481-485. DOI: 10.1002/Jhet.5570160314 |
0.478 |
|
1979 |
Rastetter WH, Adams J, Frost JW, Nummy LJ, Frommer JE, Roberts KB. On the involvement of lipoic acid in α-keto acid dehydrogenase complexes [16] Journal of the American Chemical Society. 101: 2752-2753. |
0.674 |
|
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