-
1
-
-
43049107992
-
Unearthing the roots of the terpenome
-
Christianson, D.W. Unearthing the roots of the terpenome. Curr. Opin. Chem. Biol., 2008, 12, 141-150.
-
(2008)
Curr. Opin. Chem. Biol
, vol.12
, pp. 141-150
-
-
Christianson, D.W.1
-
3
-
-
0028837082
-
Biochemistry and molecular biology of the isoprenoid biosynthetic pathway in plants
-
Chappell, J. Biochemistry and molecular biology of the isoprenoid biosynthetic pathway in plants. Annu. Rev. Plant. Phys., 1995, 46, 521-547.
-
(1995)
Annu. Rev. Plant. Phys
, vol.46
, pp. 521-547
-
-
Chappell, J.1
-
4
-
-
67651030513
-
Biosynthesis of plant isoprenoids: Perspectives for microbial engineering
-
Kirby, J.; Keasling, J.D. Biosynthesis of plant isoprenoids: Perspectives for microbial engineering. Annu. Rev. Plant. Biol., 2009, 60, 335-355.
-
(2009)
Annu. Rev. Plant. Biol
, vol.60
, pp. 335-355
-
-
Kirby, J.1
Keasling, J.D.2
-
5
-
-
84904043749
-
Rhodobacter capsulatus DXP synthase: Steady-state kinetics and substrate binding
-
Eubanks, L.M.; Poulter, C.D. Rhodobacter capsulatus DXP synthase: Steady-state kinetics and substrate binding. Biochemistry, 2001, 40, 8613-8614.
-
(2001)
Biochemistry
, vol.40
, pp. 8613-8614
-
-
Eubanks, L.M.1
Poulter, C.D.2
-
6
-
-
0037039285
-
E. coli MEP synthase: Steady-state kinetic analysis and substrate binding
-
Koppisch, A.T.; Fox, D.T.; Blagg, B.S.; Poulter, C.D. E. coli MEP synthase: steady-state kinetic analysis and substrate binding. Biochemistry, 2002, 41, 236-243.
-
(2002)
Biochemistry
, vol.41
, pp. 236-243
-
-
Koppisch, A.T.1
Fox, D.T.2
Blagg, B.S.3
Poulter, C.D.4
-
7
-
-
0034638354
-
Biosynthesis of isoprenoids. A rapid method for the preparation of isotope-labeled 4-diphosphocytidyl-2Cmethyl-D-erythritol
-
Rohdich, F.; Schuhr, C.A.; Hecht, S.; Herz, S.; Wungsintaweekul, J.; Eisenreich, W.; Zenk, M.H.; Bacher, A. Biosynthesis of isoprenoids. A rapid method for the preparation of isotope-labeled 4-diphosphocytidyl-2Cmethyl-D-erythritol. J. Am. Chem. Soc., 2000, 122, 9571-9574.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 9571-9574
-
-
Rohdich, F.1
Schuhr, C.A.2
Hecht, S.3
Herz, S.4
Wungsintaweekul, J.5
Eisenreich, W.6
Zenk, M.H.7
Bacher, A.8
-
8
-
-
0042424807
-
Biosynthesis of isoprenoids: Crystal structure of 4-diphosphocytidyl-2Cmethyl-D-erythritol kinase
-
Miallau, L.; Alphey, M.S.; Kemp, L.E.; Leonard, G.A.; McSweeney, S.M.; Hecht, S.; Bacher, A.; Eisenreich, W.; Rohdich, F.; Hunter, W.N. Biosynthesis of isoprenoids: crystal structure of 4-diphosphocytidyl-2Cmethyl-D-erythritol kinase. Proc. Natl. Acad. Sci. USA, 2003, 100, 9173-9178.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 9173-9178
-
-
Miallau, L.1
Alphey, M.S.2
Kemp, L.E.3
Leonard, G.A.4
McSweeney, S.M.5
Hecht, S.6
Bacher, A.7
Eisenreich, W.8
Rohdich, F.9
Hunter, W.N.10
-
9
-
-
0034646297
-
Biosynthesis of terpenoids: YgbB protein converts 4-diphosphocytidyl-2Cmethyl-D-erythritol 2-phosphate to 2C-methyl-D-erythritol 2, 4-cyclodiphosphate
-
Herz, S.; Wungsintaweekul, J.; Schuhr, C.A.; Hecht, S.; Luttgen, H.; Sagner, S.; Fellermeier, M.; Eisenreich, W.; Zenk, M.H.; Bacher, A.; Rohdich, F. Biosynthesis of terpenoids: YgbB protein converts 4-diphosphocytidyl-2Cmethyl-D-erythritol 2-phosphate to 2C-methyl-D-erythritol 2, 4-cyclodiphosphate. Proc. Natl. Acad. Sci. USA, 2000, 97, 2486-2490.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 2486-2490
-
-
Herz, S.1
Wungsintaweekul, J.2
Schuhr, C.A.3
Hecht, S.4
Luttgen, H.5
Sagner, S.6
Fellermeier, M.7
Eisenreich, W.8
Zenk, M.H.9
Bacher, A.10
Rohdich, F.11
-
10
-
-
34547697909
-
Isoprenoid biosynthesis via the methylerythritol phosphate pathway: GcpE and LytB, two novel iron-sulphur proteins
-
Seemann, M.; Rohmer, M. Isoprenoid biosynthesis via the methylerythritol phosphate pathway: GcpE and LytB, two novel iron-sulphur proteins. Cr. Chim., 2007, 10, 748-755.
-
(2007)
Cr. Chim
, vol.10
, pp. 748-755
-
-
Seemann, M.1
Rohmer, M.2
-
11
-
-
84884971027
-
Isopentenyl diphosphate and dimethylallyl diphosphate/isopentenyl diphosphate ratio measured with recombinant isopentenyl diphosphate isomerase and isoprene synthase
-
Zhou, C.F.; Li, Z.R.; Wiberley-Bradford, A.E.; Weise, S.E.; Sharkey, T.D. Isopentenyl diphosphate and dimethylallyl diphosphate/isopentenyl diphosphate ratio measured with recombinant isopentenyl diphosphate isomerase and isoprene synthase. Anal. Biochem., 2013, 440, 130-136.
-
(2013)
Anal. Biochem
, vol.440
, pp. 130-136
-
-
Zhou, C.F.1
Li, Z.R.2
Wiberley-Bradford, A.E.3
Weise, S.E.4
Sharkey, T.D.5
-
12
-
-
0032170425
-
The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms
-
Eisenreich, W.; Schwarz, M.; Cartayrade, A.; Arigoni, D.; Zenk, M.H.; Bacher, A. The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms. Chem. Biol., 1998, 5, R221-233.
-
(1998)
Chem. Biol
, vol.5
-
-
Eisenreich, W.1
Schwarz, M.2
Cartayrade, A.3
Arigoni, D.4
Zenk, M.H.5
Bacher, A.6
-
13
-
-
0033213706
-
The discovery of a mevalonate-independent pathway for isoprenoid biosynthesis in bacteria, algae and higher plants
-
Rohmer, M. The discovery of a mevalonate-independent pathway for isoprenoid biosynthesis in bacteria, algae and higher plants. Nat. Prod. Rep., 1999, 16, 565-74.
-
(1999)
Nat. Prod. Rep
, vol.16
, pp. 565-574
-
-
Rohmer, M.1
-
14
-
-
0033520336
-
Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs
-
Jomaa, H.; Wiesner, J.; Sanderbrand, S.; Altincicek, B.; Weidemeyer, C.; Hintz, M.; Turbachova, I.; Eberl, M.; Zeidler, J.; Lichtenthaler, H.K.; Soldati, D.; Beck, E. Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs. Science, 1999, 285, 1573-1576.
-
(1999)
Science
, vol.285
, pp. 1573-1576
-
-
Jomaa, H.1
Wiesner, J.2
Sanderbrand, S.3
Altincicek, B.4
Weidemeyer, C.5
Hintz, M.6
Turbachova, I.7
Eberl, M.8
Zeidler, J.9
Lichtenthaler, H.K.10
Soldati, D.11
Beck, E.12
-
15
-
-
0041589189
-
The methylerythritol phosphate pathway and its significance as a novel drug target
-
Testa, C.A.; Brown, M.J. The methylerythritol phosphate pathway and its significance as a novel drug target. Curr. Pharm. Biotech., 2003, 4, 248-259.
-
(2003)
Curr. Pharm. Biotech
, vol.4
, pp. 248-259
-
-
Testa, C.A.1
Brown, M.J.2
-
16
-
-
0031973418
-
Incorporation of [2,3-C-13(2)]-and [2,4-C-13(2)]-D-1-deoxyxylulose into ubiquinone of Escherichia coli via the mevalonate-independent pathway for isoprenoid biosynthesis
-
Putra, S.R.; Lois, L.M.; Campos, N.; Boronat, A.; Rohmer, M. Incorporation of [2,3-C-13(2)]-and [2,4-C-13(2)]-D-1-deoxyxylulose into ubiquinone of Escherichia coli via the mevalonate-independent pathway for isoprenoid biosynthesis. Tetrahedron Lett., 1998, 39, 23-26.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 23-26
-
-
Putra, S.R.1
Lois, L.M.2
Campos, N.3
Boronat, A.4
Rohmer, M.5
-
17
-
-
0033582687
-
A short enantioselective synthesis of 1-deoxy-L-xylulose by antibody catalysis
-
Shabat, D.; List, B.; Lerner, R.A.; Barbas, C.F. A short enantioselective synthesis of 1-deoxy-L-xylulose by antibody catalysis. Tetrahedron Lett., 1999, 40, 1437-1440.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 1437-1440
-
-
Shabat, D.1
List, B.2
Lerner, R.A.3
Barbas, C.F.4
-
18
-
-
0035356040
-
Enzyme-assisted preparation of isotope-labeled 1-deoxy-D-xylulose 5-phosphate
-
Hecht, S.; Kis, F.; Eisenreich, W.; Amslinger, S.; Wungsintaweekul, J.; Herz, S.; Rohdich, F.; Bacher, A. Enzyme-assisted preparation of isotope-labeled 1-deoxy-D-xylulose 5-phosphate. J. Org. Chem., 2001, 66, 3948-3952.
-
(2001)
J. Org. Chem
, vol.66
, pp. 3948-3952
-
-
Hecht, S.1
Kis, F.2
Eisenreich, W.3
Amslinger, S.4
Wungsintaweekul, J.5
Herz, S.6
Rohdich, F.7
Bacher, A.8
-
19
-
-
77949914576
-
Optimized enzymatic preparation of 1-deoxy-D-xylulose 5-phosphate
-
Zhou, Y.F.; Cui, Z.; Li, H.; Tian, J.; Gao, W.Y. Optimized enzymatic preparation of 1-deoxy-D-xylulose 5-phosphate. Bioorg. Chem., 2010, 38, 120-123.
-
(2010)
Bioorg. Chem
, vol.38
, pp. 120-123
-
-
Zhou, Y.F.1
Cui, Z.2
Li, H.3
Tian, J.4
Gao, W.Y.5
-
20
-
-
0019458359
-
The origin of the carbon chain in the thiazole moiety of thiamine in Escherichia coli-Incorporation of deuterated 1-deoxy-D-threo-2-pentulose
-
Therisod, M.; Fischer, J.C.; Estramareix, B. The origin of the carbon chain in the thiazole moiety of thiamine in Escherichia coli-Incorporation of deuterated 1-deoxy-D-threo-2-pentulose. Biochem. Biophys. Res. Commun., 1981, 98, 374-379.
-
(1981)
Biochem. Biophys. Res. Commun
, vol.98
, pp. 374-379
-
-
Therisod, M.1
Fischer, J.C.2
Estramareix, B.3
-
21
-
-
33845558307
-
1-Deoxy-D-threo-2-pentulose-the precursor of the 5-carbon chain of the thiazole of thiamine
-
David, S.; Estramareix, B.; Fischer, J.C.; Therisod, M. 1-Deoxy-D-threo-2-pentulose-the precursor of the 5-carbon chain of the thiazole of thiamine. J. Am. Chem. Soc., 1981, 103, 7341-7342.
-
(1981)
J. Am. Chem. Soc
, vol.103
, pp. 7341-7342
-
-
David, S.1
Estramareix, B.2
Fischer, J.C.3
Therisod, M.4
-
22
-
-
34250817330
-
The biosynthesis of thiamine-syntheses of [1,1,1,5-(H4)-H-2]-1-deoxy-D-threo-2-pentulose and incorporation of this sugar in biosynthesis of thiazole by Escherichia coli cells
-
David, S.; Estramareix, B.; Fischer, J.C.; Therisod, M. The biosynthesis of thiamine-syntheses of [1,1,1,5-(H4)-H-2]-1-deoxy-D-threo-2-pentulose and incorporation of this sugar in biosynthesis of thiazole by Escherichia coli cells. J. Chem. Soc. Perk. T 1., 1982, 2131-2137.
-
(1982)
J. Chem. Soc. Perk. T 1
, pp. 2131-2137
-
-
David, S.1
Estramareix, B.2
Fischer, J.C.3
Therisod, M.4
-
23
-
-
0028806683
-
Biosynthesis of vitamin B-6-Origin of pyridoxine by the union of 2 acyclic precursors, 1-deoxy-D-xylulose and 4-hydroxy-L-threonine
-
Kennedy, I.A.; Hill, R.E.; Pauloski, R.M.; Sayer, B.G.; Spenser, I.D. Biosynthesis of vitamin B-6-Origin of pyridoxine by the union of 2 acyclic precursors, 1-deoxy-D-xylulose and 4-hydroxy-L-threonine. J. Am. Chem. Soc., 1995, 117, 1661-1662.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 1661-1662
-
-
Kennedy, I.A.1
Hill, R.E.2
Pauloski, R.M.3
Sayer, B.G.4
Spenser, I.D.5
-
24
-
-
0032578753
-
Biosynthesis of isoprenoids in Escherichia coli: Retention of the methyl H-atoms of 1-deoxy-D-xylulose
-
Giner, J.L.; Jaun, B. Biosynthesis of isoprenoids in Escherichia coli: Retention of the methyl H-atoms of 1-deoxy-D-xylulose. Tetrahedron Lett., 1998, 39, 8021-8022.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 8021-8022
-
-
Giner, J.L.1
Jaun, B.2
-
25
-
-
9644262623
-
Practical synthesis of 1-deoxy-D-xylulose and 1-deoxy-D-xylulose 5-phosphate allowing deuterium labelling
-
Meyer, O.; Hoeffler, J.F.; Grosdemange-Billiard, C.; Rohmer, M. Practical synthesis of 1-deoxy-D-xylulose and 1-deoxy-D-xylulose 5-phosphate allowing deuterium labelling. Tetrahedron., 2004, 60, 12153-12162.
-
(2004)
Tetrahedron
, vol.60
, pp. 12153-12162
-
-
Meyer, O.1
Hoeffler, J.F.2
Grosdemange-Billiard, C.3
Rohmer, M.4
-
26
-
-
0033525674
-
Synthesis of 1-deoxy-D-xylulose and 1-deoxy-D-xylulose-5-phosphate
-
Blagg, B.S.J.; Poulter, C.D. Synthesis of 1-deoxy-D-xylulose and 1-deoxy-D-xylulose-5-phosphate. J. Org. Chem., 1999, 64, 1508-1511.
-
(1999)
J. Org. Chem
, vol.64
, pp. 1508-1511
-
-
Blagg, B.S.J.1
Poulter, C.D.2
-
27
-
-
0027347975
-
Selective perhydroxylation of squalene-taming the arithmetic demon
-
Crispino, G.A.; Ho, P.T.; Sharpless, K.B. Selective perhydroxylation of squalene-taming the arithmetic demon. Science, 1993, 259, 64-66.
-
(1993)
Science
, vol.259
, pp. 64-66
-
-
Crispino, G.A.1
Ho, P.T.2
Sharpless, K.B.3
-
28
-
-
85064438208
-
Asymmetric dihydroxylation of alphasubstituted styrene derivatives
-
Wang, Z.M.; Sharpless, K.B. Asymmetric dihydroxylation of alphasubstituted styrene derivatives. Synlett., (11), 1993, 603-604.
-
(1993)
Synlett., (11)
, pp. 603-604
-
-
Wang, Z.M.1
Sharpless, K.B.2
-
29
-
-
0001229845
-
Biosynthesis of isoprenoids in Escherichia coli: The fate of the 3-H and 4-H atoms of 1-deoxy-d-xylulose
-
Giner, J.L.; Jaun, B.; Arigoni, D. Biosynthesis of isoprenoids in Escherichia coli: The fate of the 3-H and 4-H atoms of 1-deoxy-d-xylulose. Chem. Commun. (Camb), 1998, 1857-1858.
-
(1998)
Chem. Commun. (Camb)
, pp. 1857-1858
-
-
Giner, J.L.1
Jaun, B.2
Arigoni, D.3
-
30
-
-
0030863368
-
Highly efficient and versatile synthesis of isotopically labelled 1-deoxy-D-xylulose
-
Piel, J.; Boland, W. Highly efficient and versatile synthesis of isotopically labelled 1-deoxy-D-xylulose. Tetrahedron Lett., 1997, 38, 6387-6390.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 6387-6390
-
-
Piel, J.1
Boland, W.2
-
31
-
-
0000188835
-
Chemical and enzymatic synthesis of 1-Deoxy-D-xylulose-5-phosphate
-
Taylor, S.V.; Vu, L.D.; Begley, T.P.; Schorken, U.; Grolle, S.; Sprenger, G.A.; Bringer-Meyer, S.; Sahm, H. Chemical and enzymatic synthesis of 1-Deoxy-D-xylulose-5-phosphate. J. Org. Chem., 1998, 63, 2375-2377.
-
(1998)
J. Org. Chem
, vol.63
, pp. 2375-2377
-
-
Taylor, S.V.1
Vu, L.D.2
Begley, T.P.3
Schorken, U.4
Grolle, S.5
Sprenger, G.A.6
Bringer-Meyer, S.7
Sahm, H.8
-
32
-
-
0032559979
-
New and efficient synthetic routes to 1-deoxy-D-xylulose
-
Giner, J.L. New and efficient synthetic routes to 1-deoxy-D-xylulose. Tetrahedron Lett., 1998, 39, 2479-2482.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2479-2482
-
-
Giner, J.L.1
-
33
-
-
0141526230
-
Rapid and flexible synthesis of 1-deoxy-D-xylulose-5-phosphate, the substrate for 1-deoxy-Dxylulose-5-phosphate reductoisomerase
-
Cox, R.J.; de Andres-Gomez, A.; Godfrey, C.R.A. Rapid and flexible synthesis of 1-deoxy-D-xylulose-5-phosphate, the substrate for 1-deoxy-Dxylulose-5-phosphate reductoisomerase. Org. Biomol. Chem., 2003, 1, 3173-3177.
-
(2003)
Org. Biomol. Chem
, vol.1
, pp. 3173-3177
-
-
Cox, R.J.1
de Andres-Gomez, A.2
Godfrey, C.R.A.3
-
34
-
-
34447344507
-
The chemical mechanism of D-1-deoxyxylulose-5-phosphate reductoisomerase from Escherichia coli
-
Wong, U.; Cox, R.J. The chemical mechanism of D-1-deoxyxylulose-5-phosphate reductoisomerase from Escherichia coli. Angew. Chem. Int. Ed. Engl., 2007, 46, 4926-4929.
-
(2007)
Angew. Chem. Int. Ed. Engl
, vol.46
, pp. 4926-4929
-
-
Wong, U.1
Cox, R.J.2
-
35
-
-
20444408794
-
Mechanistic studies with 2-C-methyl-D-erythritol 4-phosphate synthase from Escherichia coli
-
Fox, D.T.; Poulter, C.D. Mechanistic studies with 2-C-methyl-D-erythritol 4-phosphate synthase from Escherichia coli. Biochemistry, 2005, 44, 8360-8368.
-
(2005)
Biochemistry
, vol.44
, pp. 8360-8368
-
-
Fox, D.T.1
Poulter, C.D.2
-
36
-
-
6444226766
-
Study of 1-deoxy-D-xylulose-5-phosphate reductoisomerase: Synthesis and evaluation of fluorinated substrate analogues
-
Wong, A.; Munos, J.W.; Devasthali, V.; Johnson, K.A.; Liu, H.W. Study of 1-deoxy-D-xylulose-5-phosphate reductoisomerase: Synthesis and evaluation of fluorinated substrate analogues. Org. Lett., 2004, 6, 3625-3628.
-
(2004)
Org. Lett
, vol.6
, pp. 3625-3628
-
-
Wong, A.1
Munos, J.W.2
Devasthali, V.3
Johnson, K.A.4
Liu, H.W.5
-
37
-
-
67849094631
-
A secondary kinetic isotope effect study of the 1-deoxy-D-xylulose-5-phosphate reductoisomerase-catalyzed reaction: Evidence for a retroaldolaldol rearrangement
-
Munos, J.W.; Pu, X.T.; Mansoorabadi, S.O.; Kim, H.J.; Liu, H.W. A secondary kinetic isotope effect study of the 1-deoxy-D-xylulose-5-phosphate reductoisomerase-catalyzed reaction: Evidence for a retroaldolaldol rearrangement. J. Am. Chem. Soc., 2009, 131, 2048-2049.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 2048-2049
-
-
Munos, J.W.1
Pu, X.T.2
Mansoorabadi, S.O.3
Kim, H.J.4
Liu, H.W.5
-
38
-
-
0033588318
-
The synthesis of 1-fluoro-and 1,1-difluoroanalogues of 1-deoxy-D-xylulose
-
Bouvet, D.; O'Hagan, D. The synthesis of 1-fluoro-and 1,1-difluoroanalogues of 1-deoxy-D-xylulose. Tetrahedron, 1999, 55, 10481-10486.
-
(1999)
Tetrahedron
, vol.55
, pp. 10481-10486
-
-
Bouvet, D.1
O'Hagan, D.2
-
39
-
-
15444362202
-
Synthesis and evaluation of 1-deoxy-D-xylulose 5-phosphoric acid analogues as alternate substrates for methylerythritol phosphate synthase
-
Fox, D.T.; Poulter, C.D. Synthesis and evaluation of 1-deoxy-D-xylulose 5-phosphoric acid analogues as alternate substrates for methylerythritol phosphate synthase. J. Org. Chem., 2005, 70, 1978-1985.
-
(2005)
J. Org. Chem
, vol.70
, pp. 1978-1985
-
-
Fox, D.T.1
Poulter, C.D.2
-
40
-
-
0024293191
-
Isopentenyl-diphosphate isomerase: Inactivation of the enzyme with active-site-directed irreversible inhibitors and transition-state analogues
-
Muehlbacher, M.; Poulter, C.D. Isopentenyl-diphosphate isomerase: inactivation of the enzyme with active-site-directed irreversible inhibitors and transition-state analogues. Biochemistry, 1988, 27, 7315-7328.
-
(1988)
Biochemistry
, vol.27
, pp. 7315-7328
-
-
Muehlbacher, M.1
Poulter, C.D.2
-
41
-
-
33845183108
-
Synthetic methods and reactions. 141. Fluoride-induced trifluoromethylation of carbonylcompounds with trifluoromethyltrimethylsilane (TMS-CF3)-a trifluoromethide equivalent
-
Prakash, G.K.S.; Krishnamurti, R.; Olah, G.A. Synthetic methods and reactions. 141. Fluoride-induced trifluoromethylation of carbonylcompounds with trifluoromethyltrimethylsilane (TMS-CF3)-a trifluoromethide equivalent. J. Am. Chem. Soc., 1989, 111, 393-395.
-
(1989)
J. Am. Chem. Soc
, vol.111
, pp. 393-395
-
-
Prakash, G.K.S.1
Krishnamurti, R.2
Olah, G.A.3
-
42
-
-
0346655238
-
The sorbitol phosphotransferase system is responsible for transport of 2-C-methyl-D-erythritol into Salmonella enterica serovar typhimurium
-
Testa, C.A.; Cornish, R.A.; Poulter, C.D. The sorbitol phosphotransferase system is responsible for transport of 2-C-methyl-D-erythritol into Salmonella enterica serovar typhimurium. J. Bacteriol., 2004, 186, 473-480.
-
(2004)
J. Bacteriol
, vol.186
, pp. 473-480
-
-
Testa, C.A.1
Cornish, R.A.2
Poulter, C.D.3
-
43
-
-
0030855436
-
Incorporation of 2-C-methyl-D-erythritol, a putative isoprenoid precursor in the mevalonate-independent pathway, into ubiquinone and menaquinone of Escherichia coli
-
Duvold, T.; Cali, P.; Bravo, J.M.; Rohmer, M. Incorporation of 2-C-methyl-D-erythritol, a putative isoprenoid precursor in the mevalonate-independent pathway, into ubiquinone and menaquinone of Escherichia coli. Tetrahedron Lett., 1997, 38, 6181-6184.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 6181-6184
-
-
Duvold, T.1
Cali, P.2
Bravo, J.M.3
Rohmer, M.4
-
44
-
-
0034653549
-
Deuterium-labelled isotopomers of 2-C-methyl-Derythritol as tools for the elucidation of the 2-C-methyl-D-erythritol 4-phosphate pathway for isoprenoid biosynthesis
-
Charon, L.; Hoeffler, J.F.; Pale-Grosdemange, C.; Lois, L.M.; Campos, N.; Boronat, A.; Rohmer, M. Deuterium-labelled isotopomers of 2-C-methyl-Derythritol as tools for the elucidation of the 2-C-methyl-D-erythritol 4-phosphate pathway for isoprenoid biosynthesis. Biochem. J., 2000, 346 (Pt 3), 737-42.
-
(2000)
Biochem. J
, vol.346
, Issue.Pt 3
, pp. 737-742
-
-
Charon, L.1
Hoeffler, J.F.2
Pale-Grosdemange, C.3
Lois, L.M.4
Campos, N.5
Boronat, A.6
Rohmer, M.7
-
45
-
-
0033607440
-
Synthesis of [3,5,5,5-H-2(4)]-2-C-methyl-D-erythritol, a substrate designed for the elucidation of the mevalonate independent route for isoprenoid biosynthesis
-
Charon, L.; Hoeffler, J.F.; Pale-Grosdemange, C.; Rohmer, M. Synthesis of [3,5,5,5-H-2(4)]-2-C-methyl-D-erythritol, a substrate designed for the elucidation of the mevalonate independent route for isoprenoid biosynthesis. Tetrahedron Lett., 1999, 40, 8369-8373.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 8369-8373
-
-
Charon, L.1
Hoeffler, J.F.2
Pale-Grosdemange, C.3
Rohmer, M.4
-
46
-
-
84867838237
-
2C-Methyl-D-erythritol 4-phosphate enhances and sustains cyclodiphosphate synthase IspF activity
-
Bitok, J.K.; Meyers, C.F. 2C-Methyl-D-erythritol 4-phosphate enhances and sustains cyclodiphosphate synthase IspF activity. ACS Chem. Biol., 2012, 7, 1702-1710.
-
(2012)
ACS Chem. Biol
, vol.7
, pp. 1702-1710
-
-
Bitok, J.K.1
Meyers, C.F.2
-
47
-
-
0037698100
-
Cross-talk between the cytosolic mevalonate and the plastidial methylerythritol phosphate pathways in Tobacco Bright Yellow-2 cells
-
Hemmerlin, A.; Hoeffler, J.F.; Meyer, O.; Tritsch, D.; Kagan, I.A.; Grosdemange-Billiard, C.; Rohmer, M.; Bach, T.J. Cross-talk between the cytosolic mevalonate and the plastidial methylerythritol phosphate pathways in Tobacco Bright Yellow-2 cells. J. Biol. Chem., 2003, 278, 26666-26676.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 26666-26676
-
-
Hemmerlin, A.1
Hoeffler, J.F.2
Meyer, O.3
Tritsch, D.4
Kagan, I.A.5
Grosdemange-Billiard, C.6
Rohmer, M.7
Bach, T.J.8
-
48
-
-
0032543467
-
Direct formation of 2-C-methyl-D-erythritol 4-phosphate from 1-deoxy-D-xylulose 5-phosphate by 1-deoxy-D-xylulose 5-phosphate reductoisomerase, a new enzyme in the non-mevalonate pathway to isopentenyl diphosphate
-
Kuzuyama, T.; Takahashi, S.; Watanabe, H.; Seto, H. Direct formation of 2-C-methyl-D-erythritol 4-phosphate from 1-deoxy-D-xylulose 5-phosphate by 1-deoxy-D-xylulose 5-phosphate reductoisomerase, a new enzyme in the non-mevalonate pathway to isopentenyl diphosphate. Tetrahedron Lett., 1998, 39, 4509-4512.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4509-4512
-
-
Kuzuyama, T.1
Takahashi, S.2
Watanabe, H.3
Seto, H.4
-
49
-
-
0032499047
-
Biosynthesis of 2-C-methyl-D-erythritol in plants by rearrangement of the terpenoid precursor, 1-deoxy-D-xylulose 5-phosphate
-
Sagner, S.; Eisenreich, W.; Fellermeier, M.; Latzel, C.; Bacher, A.; Zenk, M.H. Biosynthesis of 2-C-methyl-D-erythritol in plants by rearrangement of the terpenoid precursor, 1-deoxy-D-xylulose 5-phosphate. Tetrahedron Lett., 1998, 39, 2091-2094.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2091-2094
-
-
Sagner, S.1
Eisenreich, W.2
Fellermeier, M.3
Latzel, C.4
Bacher, A.5
Zenk, M.H.6
-
50
-
-
48249127143
-
Spatial and seasonal trends in biogenic secondary organic aerosol tracers and water-soluble organic carbon in the southeastern United States
-
Ding, X.; Zheng, M.; Yu, L.P.; Zhang, X.L.; Weber, R.J.; Yan, B.; Russell, A.G.; Edgerton, E.S.; Wang, X.M. Spatial and seasonal trends in biogenic secondary organic aerosol tracers and water-soluble organic carbon in the southeastern United States. Environ. Sci. Technol., 2008, 42, 5171-5176.
-
(2008)
Environ. Sci. Technol
, vol.42
, pp. 5171-5176
-
-
Ding, X.1
Zheng, M.2
Yu, L.P.3
Zhang, X.L.4
Weber, R.J.5
Yan, B.6
Russell, A.G.7
Edgerton, E.S.8
Wang, X.M.9
-
51
-
-
77955629922
-
Development of a compound-specific carbon isotope analysis method for 2-methyltetrols, biomarkers for secondary organic aerosols from atmospheric isoprene
-
Li, Q.A.; Wang, W.; Zhang, H.W.; Wang, Y.J.; Wang, B.; Li, L.; Li, H.J.; Wang, B.J.; Zhan, J.; Wu, M.; Bi, X.H. Development of a compound-specific carbon isotope analysis method for 2-methyltetrols, biomarkers for secondary organic aerosols from atmospheric isoprene. Anal. Chem., 2010, 82, 6764-6769.
-
(2010)
Anal. Chem
, vol.82
, pp. 6764-6769
-
-
Li, Q.A.1
Wang, W.2
Zhang, H.W.3
Wang, Y.J.4
Wang, B.5
Li, L.6
Li, H.J.7
Wang, B.J.8
Zhan, J.9
Wu, M.10
Bi, X.H.11
-
52
-
-
33751096731
-
Seasonal variation of 2-methyltetrols in ambient air samples
-
Xia, X.; Hopke, P.K. Seasonal variation of 2-methyltetrols in ambient air samples. Environ. Sci. Technol., 2006, 40, 6934-6937.
-
(2006)
Environ. Sci. Technol
, vol.40
, pp. 6934-6937
-
-
Xia, X.1
Hopke, P.K.2
-
53
-
-
0021764536
-
Synthesis of 3-C-(hydroxymethyl)erythritol and 3-C-methylerythritol
-
Witczak, Z.J.; Whistler, R.L. Synthesis of 3-C-(hydroxymethyl)erythritol and 3-C-methylerythritol. Carbohydr. Res., 1984, 133, 235-245.
-
(1984)
Carbohydr. Res
, vol.133
, pp. 235-245
-
-
Witczak, Z.J.1
Whistler, R.L.2
-
54
-
-
0030960034
-
Biosynthesis of 2-C-methyl-D-erythritol, a putative C-5 intermediate in the mevalonate independent pathway for isoprenoid biosynthesis
-
Duvold, T.; Bravo, J.M.; PaleGrosdemange, C.; Rohmer, M. Biosynthesis of 2-C-methyl-D-erythritol, a putative C-5 intermediate in the mevalonate independent pathway for isoprenoid biosynthesis. Tetrahedron Lett., 1997, 38, 4769-4772.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 4769-4772
-
-
Duvold, T.1
Bravo, J.M.2
Palegrosdemange, C.3
Rohmer, M.4
-
55
-
-
4444276636
-
Catalytic asymmetric dihydroxylation
-
Kolb, H.C.; Vannieuwenhze, M.S.; Sharpless, K.B. Catalytic asymmetric dihydroxylation. Chem. Rev., 1994, 94, 2483-2547.
-
(1994)
Chem. Rev
, vol.94
, pp. 2483-2547
-
-
Kolb, H.C.1
Vannieuwenhze, M.S.2
Sharpless, K.B.3
-
56
-
-
0034706352
-
Simple and versatile synthesis of branched polyols: (+)-2-C-methylerythritol and (+)-2-Cmethylthreitol
-
Fontana, A.; Messina, R.; Spinella, A.; Cimino, G. Simple and versatile synthesis of branched polyols: (+)-2-C-methylerythritol and (+)-2-Cmethylthreitol. Tetrahedron Lett., 2000, 41, 7559-7562.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 7559-7562
-
-
Fontana, A.1
Messina, R.2
Spinella, A.3
Cimino, G.4
-
57
-
-
33645755803
-
Asymmetric synthesis of four isomers of 2-C-trifluoromethylerythritol
-
Wang, H.; Zhao, X.M.; Li, Y.H.; Lu, L. Asymmetric synthesis of four isomers of 2-C-trifluoromethylerythritol. J. Org. Chem., 2006, 71, 3278-3281.
-
(2006)
J. Org. Chem
, vol.71
, pp. 3278-3281
-
-
Wang, H.1
Zhao, X.M.2
Li, Y.H.3
Lu, L.4
-
58
-
-
84860218200
-
Synthesis of 2-C-methylerythritols and 2-C-methylthreitols via enantiodivergent sharp less dihydroxylation of trisubstituted olefins
-
Ghosh, S.K.; Butler, M.S.; Lear, M.J. Synthesis of 2-C-methylerythritols and 2-C-methylthreitols via enantiodivergent sharp less dihydroxylation of trisubstituted olefins. Tetrahedron Lett., 2012, 53, 2706-2708.
-
(2012)
Tetrahedron Lett
, vol.53
, pp. 2706-2708
-
-
Ghosh, S.K.1
Butler, M.S.2
Lear, M.J.3
-
59
-
-
0034719257
-
Synthesis of 2-C-methyl-Derythritol 4-phosphate: The first pathway-specific intermediate in the methylerythritol phosphate route to isoprenoids
-
Koppisch, A.T.; Blagg, B.S.J.; Poulter, C.D. Synthesis of 2-C-methyl-Derythritol 4-phosphate: The first pathway-specific intermediate in the methylerythritol phosphate route to isoprenoids. Org. Lett., 2000, 2, 215-217.
-
(2000)
Org. Lett
, vol.2
, pp. 215-217
-
-
Koppisch, A.T.1
Blagg, B.S.J.2
Poulter, C.D.3
-
60
-
-
0037178358
-
Synthesis of 4-diphosphocytidyl-2-C-methyl-D-erythritol and 2-C-methyl-D-erythritol-4-phosphate
-
Koppisch, A.T.; Poulter, C.D. Synthesis of 4-diphosphocytidyl-2-C-methyl-D-erythritol and 2-C-methyl-D-erythritol-4-phosphate. J. Org. Chem., 2002, 67, 5416-5418.
-
(2002)
J. Org. Chem
, vol.67
, pp. 5416-5418
-
-
Koppisch, A.T.1
Poulter, C.D.2
-
61
-
-
67650556276
-
Dihydroxylation of 4-substituted 1,2-dioxines: A concise route to branched erythro sugars
-
Robinson, T.V.; Pedersen, D.S.; Taylor, D.K.; Tiekink, E.R.T. Dihydroxylation of 4-substituted 1,2-dioxines: A concise route to branched erythro sugars. J. Org. Chem., 2009, 74, 5093-5096.
-
(2009)
J. Org. Chem
, vol.74
, pp. 5093-5096
-
-
Robinson, T.V.1
Pedersen, D.S.2
Taylor, D.K.3
Tiekink, E.R.T.4
-
62
-
-
0034723315
-
An efficient preparation of 2-C-methyl-D-erythritol 4-phosphoric acid and its derivatives
-
Kis, K.; Wungsintaweekul, J.; Eisenreich, W.; Zenk, M.H.; Bacher, A. An efficient preparation of 2-C-methyl-D-erythritol 4-phosphoric acid and its derivatives. J. Org. Chem., 2000, 65, 587-592.
-
(2000)
J. Org. Chem
, vol.65
, pp. 587-592
-
-
Kis, K.1
Wungsintaweekul, J.2
Eisenreich, W.3
Zenk, M.H.4
Bacher, A.5
-
63
-
-
0034686339
-
Synthesis of tritium labelled 2-C-methyl-D-erythritol, a useful substrate for the elucidation of the methylerythritol phosphate pathway for isoprenoid biosynthesis
-
Hoeffler, J.F.; Grosdemange-Billiard, C.; Rohmer, M. Synthesis of tritium labelled 2-C-methyl-D-erythritol, a useful substrate for the elucidation of the methylerythritol phosphate pathway for isoprenoid biosynthesis. Tetrahedron Lett., 2000, 41, 4885-4889.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 4885-4889
-
-
Hoeffler, J.F.1
Grosdemange-Billiard, C.2
Rohmer, M.3
-
64
-
-
0034629271
-
Chemical synthesis of enantiopure 2-C-methyl-D-erythritol 4-phosphate, the key intermediate in the mevalonate-independent pathway for isoprenoid biosynthesis
-
Hoeffler, J.F.; Pale-Grosdemange, C.; Rohmer, M. Chemical synthesis of enantiopure 2-C-methyl-D-erythritol 4-phosphate, the key intermediate in the mevalonate-independent pathway for isoprenoid biosynthesis. Tetrahedron, 2000, 56, 1485-1489.
-
(2000)
Tetrahedron
, vol.56
, pp. 1485-1489
-
-
Hoeffler, J.F.1
Pale-Grosdemange, C.2
Rohmer, M.3
-
65
-
-
37549033935
-
The dioxanone approach to (2S, 3R)-2-C-methylerythritol 4-phosphate and 2, 4-cyclodiphosphate, and various MEP analogues
-
Lagisetti, C.; Urbansky, M.; Coates, R.M. The dioxanone approach to (2S, 3R)-2-C-methylerythritol 4-phosphate and 2, 4-cyclodiphosphate, and various MEP analogues. J. Org. Chem., 2007, 72, 9886-9895.
-
(2007)
J. Org. Chem
, vol.72
, pp. 9886-9895
-
-
Lagisetti, C.1
Urbansky, M.2
Coates, R.M.3
-
66
-
-
0742286897
-
Synthesis of enantiopure 2-C-methyl-D-erythritol 4-phosphate and 2, 4-cyclodiphosphate from D-arabitol
-
Urbansky, M.; Davis, C.E.; Surjan, J.D.; Coates, R.M. Synthesis of enantiopure 2-C-methyl-D-erythritol 4-phosphate and 2, 4-cyclodiphosphate from D-arabitol. Org. Lett., 2004, 6, 135-138.
-
(2004)
Org. Lett
, vol.6
, pp. 135-138
-
-
Urbansky, M.1
Davis, C.E.2
Surjan, J.D.3
Coates, R.M.4
-
67
-
-
84866046988
-
Formal synthesis of 4-diphosphocytidyl-2-C-methyl D-erythritol from D-(+)-arabitol
-
Odejinmi, S.I.; Rascon, R.G.; Chen, W.; Lai, K. Formal synthesis of 4-diphosphocytidyl-2-C-methyl D-erythritol from D-(+)-arabitol. Tetrahedron, 2012, 68, 8937-8941.
-
(2012)
Tetrahedron
, vol.68
, pp. 8937-8941
-
-
Odejinmi, S.I.1
Rascon, R.G.2
Chen, W.3
Lai, K.4
-
68
-
-
53649104910
-
Concise asymmetric syntheses of the (+)-2-C-methyltetritol isomers
-
Sharma, A.; Das, P.; Chattopadhyay, S. Concise asymmetric syntheses of the (+)-2-C-methyltetritol isomers. Tetrahedron: Asymmetry, 2008, 19, 2167-2170.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 2167-2170
-
-
Sharma, A.1
Das, P.2
Chattopadhyay, S.3
-
69
-
-
0034719257
-
Synthesis of 2-C-methyl-Derythritol 4-phosphate: The first pathway-specific intermediate in the methylerythritol phosphate route to isoprenoids
-
Koppisch, A.T.; Blagg, B.S.; Poulter, C.D. Synthesis of 2-C-methyl-Derythritol 4-phosphate: the first pathway-specific intermediate in the methylerythritol phosphate route to isoprenoids. Org Lett., 2000, 2, 215-217.
-
(2000)
Org Lett
, vol.2
, pp. 215-217
-
-
Koppisch, A.T.1
Blagg, B.S.2
Poulter, C.D.3
-
70
-
-
0027465280
-
Asymmetric dihydroxylation (Ad) of N, NDIALKYL and N-methoxy-N-methyl alpha, beta-unsaturated and beta, gamma-unsaturated amides
-
Bennani, Y.L.; Sharpless, K.B. Asymmetric dihydroxylation (Ad) of N, NDIALKYL and N-methoxy-N-methyl alpha, beta-unsaturated and beta, gamma-unsaturated amides. Tetrahedron Lett., 1993, 34, 2079-2082.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 2079-2082
-
-
Bennani, Y.L.1
Sharpless, K.B.2
-
71
-
-
0035815147
-
Concise synthesis of (+)-2-C-methyl-D-erythritol-4-phosphate
-
Fontana, A. Concise synthesis of (+)-2-C-methyl-D-erythritol-4-phosphate. J. Org. Chem., 2001, 66, 2506-2508.
-
(2001)
J. Org. Chem
, vol.66
, pp. 2506-2508
-
-
Fontana, A.1
-
72
-
-
0034723315
-
An efficient preparation of 2-C-methyl-D-erythritol 4-phosphoric acid and its derivatives
-
Kis, K.; Wungsintaweekul, J.; Eisenreich, W.; Zenk, M.H.; Bacher, A. An efficient preparation of 2-C-methyl-D-erythritol 4-phosphoric acid and its derivatives. J. Org. Chem., 2000, 65, 587-592.
-
(2000)
J. Org. Chem
, vol.65
, pp. 587-592
-
-
Kis, K.1
Wungsintaweekul, J.2
Eisenreich, W.3
Zenk, M.H.4
Bacher, A.5
-
73
-
-
0347624537
-
(3R, 4S)-3, 4, 5-trihydroxy-4-methylpentylphosphonic acid, an isosteric phosphonate analogue of 2-C-methyl-D-erythritol 4-phosphate, a key intermediate in the new pathway for isoprenoid biosynthesis
-
Hirsch, G.; Grosdemange-Billiard, C.; Tritsch, D.; Rohmer, M. (3R, 4S)-3, 4, 5-trihydroxy-4-methylpentylphosphonic acid, an isosteric phosphonate analogue of 2-C-methyl-D-erythritol 4-phosphate, a key intermediate in the new pathway for isoprenoid biosynthesis. Tetrahedron Lett., 2004, 45, 519-521.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 519-521
-
-
Hirsch, G.1
Grosdemange-Billiard, C.2
Tritsch, D.3
Rohmer, M.4
-
74
-
-
33846614463
-
A convenient synthesis of 2-Cmethyl-D-erythritol 4-phosphate and isotopomers of its precursor
-
Koumbis, A.E.; Kotoulas, S.S.; Gallos, J.K. A convenient synthesis of 2-Cmethyl-D-erythritol 4-phosphate and isotopomers of its precursor. Tetrahedron, 2007, 63, 2235-2243.
-
(2007)
Tetrahedron
, vol.63
, pp. 2235-2243
-
-
Koumbis, A.E.1
Kotoulas, S.S.2
Gallos, J.K.3
-
75
-
-
0348210598
-
Regioselective manipulation of hydroxyl groups via organotin derivatives
-
David, S.; Hanessian, S. Regioselective manipulation of hydroxyl groups via organotin derivatives. Tetrahedron, 1985, 41, 643-663.
-
(1985)
Tetrahedron
, vol.41
, pp. 643-663
-
-
David, S.1
Hanessian, S.2
-
76
-
-
77049099840
-
Synthesis of 4-diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate and kinetic studies of Mycobacterium tuberculosis IspF
-
Narayanasamy, P.; Eoh, H.; Brennan, P.J.; Crick, D.C. Synthesis of 4-diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate and kinetic studies of Mycobacterium tuberculosis IspF. Chem. Biol., 2010, 17, 117-122.
-
(2010)
Chem. Biol
, vol.17
, pp. 117-122
-
-
Narayanasamy, P.1
Eoh, H.2
Brennan, P.J.3
Crick, D.C.4
-
77
-
-
44749086415
-
Chemoenzymatic synthesis of 4-diphosphocytidyl-2-C-methyl-D-erythritol: A substrate for IspE
-
Narayanasamy, P.; Eoh, H.; Crick, D.C. Chemoenzymatic synthesis of 4-diphosphocytidyl-2-C-methyl-D-erythritol: a substrate for IspE. Tetrahedron Lett., 2008, 49, 4461-4463.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 4461-4463
-
-
Narayanasamy, P.1
Eoh, H.2
Crick, D.C.3
-
78
-
-
0035833723
-
Improved chemical synthesis of UDPgalactofuranose
-
Marlow, A.L.; Kiessling, L.L. Improved chemical synthesis of UDPgalactofuranose. Org. Lett., 2001, 3, 2517-2519.
-
(2001)
Org. Lett
, vol.3
, pp. 2517-2519
-
-
Marlow, A.L.1
Kiessling, L.L.2
-
79
-
-
0037018469
-
Synthesis of 2-C-methyl-D-erythritol 2,4-cyclopyrophosphate
-
Giner, J.L.; Ferris, W.V. Synthesis of 2-C-methyl-D-erythritol 2,4-cyclopyrophosphate. Org. Lett., 2002, 4, 1225-1226.
-
(2002)
Org. Lett
, vol.4
, pp. 1225-1226
-
-
Giner, J.L.1
Ferris, W.V.2
-
80
-
-
0037067539
-
Synthesis of (E)-4-hydroxydimethylallyl diphosphate. An intermediate in the methyl erythritol phosphate branch of the isoprenoid pathway
-
Fox, D.T.; Poulter, C.D. Synthesis of (E)-4-hydroxydimethylallyl diphosphate. An intermediate in the methyl erythritol phosphate branch of the isoprenoid pathway. J. Org. Chem., 2002, 67, 5009-10.
-
(2002)
J. Org. Chem
, vol.67
, pp. 5009-5010
-
-
Fox, D.T.1
Poulter, C.D.2
-
81
-
-
0037189202
-
Biosynthesis of terpenes. Preparation of (E)-1-Hydroxy-2-methyl-but-2-enyl 4-diphosphate, an intermediate of the deoxyxylulose phosphate pathway
-
Amslinger, S.; Kis, K.; Hecht, S.; Adam, P.; Rohdich, F.; Arigoni, D.; Bacher, A.; Eisenreich, W. Biosynthesis of terpenes. Preparation of (E)-1-Hydroxy-2-methyl-but-2-enyl 4-diphosphate, an intermediate of the deoxyxylulose phosphate pathway. J. Org. Chem., 2002, 67, 4590-4594.
-
(2002)
J. Org. Chem
, vol.67
, pp. 4590-4594
-
-
Amslinger, S.1
Kis, K.2
Hecht, S.3
Adam, P.4
Rohdich, F.5
Arigoni, D.6
Bacher, A.7
Eisenreich, W.8
-
82
-
-
0036009475
-
Synthesis of (2E)-4-hydroxy-3-methylbut-2-enyl diphosphate, a key intermediate in the biosynthesis of isoprenoids
-
Ward, J.L.; Beale, M.H. Synthesis of (2E)-4-hydroxy-3-methylbut-2-enyl diphosphate, a key intermediate in the biosynthesis of isoprenoids. J. Chem. Soc. Perk. T. 1, 2002, 710-712.
-
(2002)
J. Chem. Soc. Perk. T
, vol.1
, pp. 710-712
-
-
Ward, J.L.1
Beale, M.H.2
-
83
-
-
0037194169
-
A convenient synthesis of (E)-4-hydroxy-3-methyl-2-butenyl pyrophosphate and its [4-C-13]-labeled form
-
Giner, J.L. A convenient synthesis of (E)-4-hydroxy-3-methyl-2-butenyl pyrophosphate and its [4-C-13]-labeled form. Tetrahedron Lett., 2002, 43, 5457-5459.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5457-5459
-
-
Giner, J.L.1
-
84
-
-
0037099376
-
(E)-4-hydroxy-3-methylbut-2-enyl diphosphate: An intermediate in the formation of terpenoids in plant chromoplasts
-
Gao, W.Y.; Loeser, R.; Raschke, M.; Dessoy, M.A.; Fulhorst, M.; Alpermann, H.; Wessjohann, L.A.; Zenk, M.H. (E)-4-hydroxy-3-methylbut-2-enyl diphosphate: An intermediate in the formation of terpenoids in plant chromoplasts. Angew. Chem. Int. Ed. Engl., 2002, 41, 2604-2607.
-
(2002)
Angew. Chem. Int. Ed. Engl
, vol.41
, pp. 2604-2607
-
-
Gao, W.Y.1
Loeser, R.2
Raschke, M.3
Dessoy, M.A.4
Fulhorst, M.5
Alpermann, H.6
Wessjohann, L.A.7
Zenk, M.H.8
-
85
-
-
0037010787
-
Studies on the non-mevalonate isoprenoid biosynthetic pathway. Simple methods for preparation of isotopelabeled (E)-1-hydroxy-2-methylbut-2-enyl 4-diphosphate
-
Hecht, S.; Amslinger, S.; Jauch, J.; Kis, K.; Trentinaglia, V.; Adam, P.; Eisenreich, W.; Bacher, A.; Rohdich, F. Studies on the non-mevalonate isoprenoid biosynthetic pathway. Simple methods for preparation of isotopelabeled (E)-1-hydroxy-2-methylbut-2-enyl 4-diphosphate. Tetrahedron Lett., 2002, 43, 8929-8933.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 8929-8933
-
-
Hecht, S.1
Amslinger, S.2
Jauch, J.3
Kis, K.4
Trentinaglia, V.5
Adam, P.6
Eisenreich, W.7
Bacher, A.8
Rohdich, F.9
-
86
-
-
0036532443
-
Isoprenoid biosynthesis via the methylerythritol phosphate pathway. (E)-4-hydroxy-3-methylbut-2-enyl diphosphate: Chemical synthesis and formation from methylerythritol cyclodiphosphate by a cell-free system from Escherichia coli
-
Wolff, M.; Seemann, M.; Grosdemange-Billiard, C.; Tritsch, D.; Campos, N.; Rodriguez-Concepcion, M.; Boronat, A.; Rohmer, M. Isoprenoid biosynthesis via the methylerythritol phosphate pathway. (E)-4-hydroxy-3-methylbut-2-enyl diphosphate: chemical synthesis and formation from methylerythritol cyclodiphosphate by a cell-free system from Escherichia coli. Tetrahedron Lett., 2002, 43, 2555-2559.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 2555-2559
-
-
Wolff, M.1
Seemann, M.2
Grosdemange-Billiard, C.3
Tritsch, D.4
Campos, N.5
Rodriguez-Concepcion, M.6
Boronat, A.7
Rohmer, M.8
-
87
-
-
0037067539
-
Synthesis of (E)-4-hydroxydimethylallyl diphosphate. An intermediate in the methyl erythritol phosphate branch of the isoprenoid pathway
-
Fox, D.T.; Poulter, C.D. Synthesis of (E)-4-hydroxydimethylallyl diphosphate. An intermediate in the methyl erythritol phosphate branch of the isoprenoid pathway. J. Org. Chem., 2002, 67, 5009-5010.
-
(2002)
J. Org. Chem
, vol.67
, pp. 5009-5010
-
-
Fox, D.T.1
Poulter, C.D.2
-
88
-
-
0037022221
-
Studies on the nonmevalonate terpene biosynthetic pathway: Metabolic role of IspH (LytB) protein
-
Rohdich, F.; Hecht, S.; Gartner, K.; Adam, P.; Krieger, C.; Amslinger, S.; Arigoni, D.; Bacher, A.; Eisenreich, W. Studies on the nonmevalonate terpene biosynthetic pathway: Metabolic role of IspH (LytB) protein. Proc. Natl. Acad. Sci. U S A, 2002, 99, 1158-1163.
-
(2002)
Proc. Natl. Acad. Sci. U S A
, vol.99
, pp. 1158-1163
-
-
Rohdich, F.1
Hecht, S.2
Gartner, K.3
Adam, P.4
Krieger, C.5
Amslinger, S.6
Arigoni, D.7
Bacher, A.8
Eisenreich, W.9
-
89
-
-
0000035949
-
Synthese von geranyl-pyrophospat und farnesylpyrophosphat
-
Cramer, F.; Bohm, W. Synthese von geranyl-pyrophospat und farnesylpyrophosphat. Angew. Chem. Int. Edit., 1959, 71, 775-775.
-
(1959)
Angew. Chem. Int. Edit
, vol.71
, pp. 775
-
-
Cramer, F.1
Bohm, W.2
-
90
-
-
33845374468
-
Phosphorylation of isoprenoid alcohols
-
Davisson, V.J.; Woodside, A.B.; Neal, T.R.; Stremler, K.E.; Muehlbacher, M.; Poulter, C.D. Phosphorylation of isoprenoid alcohols. J. Org. Chem., 1986, 51, 4768-4779.
-
(1986)
J. Org. Chem
, vol.51
, pp. 4768-4779
-
-
Davisson, V.J.1
Woodside, A.B.2
Neal, T.R.3
Stremler, K.E.4
Muehlbacher, M.5
Poulter, C.D.6
-
91
-
-
0021977216
-
Synthesis of allylic and homoallylic isoprenoid pyrophosphates
-
Davisson, V.J.; Woodside, A.B.; Poulter, C.D. Synthesis of allylic and homoallylic isoprenoid pyrophosphates. Method. Enzymol., 1985, 110, 130-144.
-
(1985)
Method. Enzymol
, vol.110
, pp. 130-144
-
-
Davisson, V.J.1
Woodside, A.B.2
Poulter, C.D.3
-
92
-
-
34347396408
-
Revealing coupling patterns in isoprenoid alkylation biocatalysis
-
Walsh, C.T. Revealing coupling patterns in isoprenoid alkylation biocatalysis. ACS Chem. Biol., 2007, 2, 296-298.
-
(2007)
ACS Chem. Biol
, vol.2
, pp. 296-298
-
-
Walsh, C.T.1
-
93
-
-
34147178365
-
Chimeras of two isoprenoid synthases catalyze all four coupling reactions in isoprenoid biosynthesis
-
Thulasiram, H.V.; Erickson, H.K.; Poulter, C.D. Chimeras of two isoprenoid synthases catalyze all four coupling reactions in isoprenoid biosynthesis. Science, 2007, 316, 73-76.
-
(2007)
Science
, vol.316
, pp. 73-76
-
-
Thulasiram, H.V.1
Erickson, H.K.2
Poulter, C.D.3
-
94
-
-
39049120483
-
A common mechanism for branching, cyclopropanation, and cyclobutanation reactions in the isoprenoid biosynthetic pathway
-
Thulasiram, H.V.; Erickson, H.K.; Poulter, C.D. A common mechanism for branching, cyclopropanation, and cyclobutanation reactions in the isoprenoid biosynthetic pathway. J. Am. Chem. Soc., 2008, 130, 1966-1971.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 1966-1971
-
-
Thulasiram, H.V.1
Erickson, H.K.2
Poulter, C.D.3
-
95
-
-
0029328325
-
Terpenoid metabolism
-
Mcgarvey, D.J.; Croteau, R. Terpenoid metabolism. Plant Cell., 1995, 7, 1015-1026.
-
(1995)
Plant Cell
, vol.7
, pp. 1015-1026
-
-
McGarvey, D.J.1
Croteau, R.2
-
96
-
-
84873105503
-
Metabolic engineering of plant monoterpenes, sesquiterpenes and diterpenes-current status and future opportunities
-
Lange, B.M.; Ahkami, A. Metabolic engineering of plant monoterpenes, sesquiterpenes and diterpenes-current status and future opportunities. Plant Biotechnol. J., 2013, 11, 169-196.
-
(2013)
Plant Biotechnol. J
, vol.11
, pp. 169-196
-
-
Lange, B.M.1
Ahkami, A.2
-
97
-
-
85050056091
-
The synthesis of monoterpenes 1980-1986
-
ApSimon, J., Ed.; John Wiley & Sons, Inc.: Hoboken
-
Thomas, A.F.; Bessiere, Y. The synthesis of monoterpenes 1980-1986. In: The Total Synthesis of Natural Products; ApSimon, J., Ed.; John Wiley & Sons, Inc.: Hoboken, 1988; Vol. 7, pp. 274-454.
-
(1988)
The Total Synthesis of Natural Products
, vol.7
, pp. 274-454
-
-
Thomas, A.F.1
Bessiere, Y.2
-
98
-
-
24644435505
-
New strategies for the synthesis of monoterpene indole alkaloids
-
Borschberg, H.R. New strategies for the synthesis of monoterpene indole alkaloids. Curr. Org. Chem., 2005, 9, 1465-1491.
-
(2005)
Curr. Org. Chem
, vol.9
, pp. 1465-1491
-
-
Borschberg, H.R.1
-
99
-
-
0031838383
-
Recent applications of catalytic metal-mediated carbocyclizations in asymmetric synthesis
-
Takacs, J.M.; Boito, S.C.; Myoung, Y.C. Recent applications of catalytic metal-mediated carbocyclizations in asymmetric synthesis. Curr. Org. Chem., 1998, 2, 233-254.
-
(1998)
Curr. Org. Chem
, vol.2
, pp. 233-254
-
-
Takacs, J.M.1
Boito, S.C.2
Myoung, Y.C.3
-
100
-
-
0035650017
-
Flexible synthetic approaches to monoterpene indole alkaloids
-
Frauenfelder, C.; Schmid, G.A.; Vogelsang, T.; Borschberg, H.J. Flexible synthetic approaches to monoterpene indole alkaloids. Chimia., 2001, 55, 828-830.
-
(2001)
Chimia
, vol.55
, pp. 828-830
-
-
Frauenfelder, C.1
Schmid, G.A.2
Vogelsang, T.3
Borschberg, H.J.4
-
103
-
-
0022079803
-
Camphor-A chiral starting material in natural product synthesis
-
Money, T. Camphor-A chiral starting material in natural product synthesis. Nat. Prod. Rep., 1985, 2, 253-289.
-
(1985)
Nat. Prod. Rep
, vol.2
, pp. 253-289
-
-
Money, T.1
-
105
-
-
49549172753
-
Total synthesis of (+/-) alpha-pinene and (+/-) beta-pinene-general route to bicyclo[3.1.1]heptanes
-
Thomas, M.T.; Fallis, A.G. Total synthesis of (+/-) alpha-pinene and (+/-) beta-pinene-general route to bicyclo[3.1.1]heptanes. Tetrahedron Lett., 1973, 4687-4690.
-
(1973)
Tetrahedron Lett
, pp. 4687-4690
-
-
Thomas, M.T.1
Fallis, A.G.2
-
106
-
-
0343027847
-
Intramolecular [2 + 2] cyclo-additions of ketenes. 2. Synthesis of chrysanthenone, beta-pinene, beta-cis-bergamotene, and beta-trans-Bergamotene
-
Kulkarni, Y.S.; Snider, B.B. Intramolecular [2 + 2] cyclo-additions of ketenes. 2. Synthesis of chrysanthenone, beta-pinene, beta-cis-bergamotene, and beta-trans-Bergamotene. J. Org. Chem., 1985, 50, 2809-2810.
-
(1985)
J. Org. Chem
, vol.50
, pp. 2809-2810
-
-
Kulkarni, Y.S.1
Snider, B.B.2
-
107
-
-
84878843572
-
Review of some investigations of chemistry of carene
-
Cocker, W. Review of some investigations of chemistry of carene. J. Soc. Cosmet. Chem., 1971, 22, 249-284.
-
(1971)
J. Soc. Cosmet. Chem
, vol.22
, pp. 249-284
-
-
Cocker, W.1
-
108
-
-
0001022113
-
Synthesis of fused cyclopropanes from gammastannyl alcohols
-
Kadow, J.F.; Johnson, C.R. Synthesis of fused cyclopropanes from gammastannyl alcohols. Tetrahedron Lett., 1984, 25, 5255-5258.
-
(1984)
Tetrahedron Lett
, vol.25
, pp. 5255-5258
-
-
Kadow, J.F.1
Johnson, C.R.2
-
109
-
-
28444447976
-
Use of monoterpenes, 3-carene and 2-carene, as synthons in the stereoselective synthesis of 2,2-dimethyl-1,3-disubstituted cyclopropanes
-
Macaev, F.Z.; Malkov, A.V. Use of monoterpenes, 3-carene and 2-carene, as synthons in the stereoselective synthesis of 2,2-dimethyl-1,3-disubstituted cyclopropanes. Tetrahedron., 2006, 62, 9-29.
-
(2006)
Tetrahedron
, vol.62
, pp. 9-29
-
-
Macaev, F.Z.1
Malkov, A.V.2
-
110
-
-
80054071903
-
Perspectives on sesquiterpene lactones in inflammation and cancer
-
Merfort, I. Perspectives on sesquiterpene lactones in inflammation and cancer. Curr. Drug Targets, 2011, 12, 1560-1573.
-
(2011)
Curr. Drug Targets
, vol.12
, pp. 1560-1573
-
-
Merfort, I.1
-
111
-
-
0024376173
-
Ras oncogenes in human cancer-a review
-
Bos, J.L. Ras oncogenes in human cancer-a review. Cancer Res., 1989, 49, 4682-4689.
-
(1989)
Cancer Res
, vol.49
, pp. 4682-4689
-
-
Bos, J.L.1
-
112
-
-
0034007935
-
Recent studies of the mechanism of protein prenylation
-
Harris, C.M.; Poulter, C.D. Recent studies of the mechanism of protein prenylation. Nat. Prod. Rep., 2000, 17, 137-144.
-
(2000)
Nat. Prod. Rep
, vol.17
, pp. 137-144
-
-
Harris, C.M.1
Poulter, C.D.2
-
113
-
-
0036517177
-
Inhibitors of protein farnesyltransferase as novel anticancer agents
-
Ohkanda, J.; Knowles, D.B.; Blaskovich, M.A.; Sebti, S.M.; Hamilton, A.D. Inhibitors of protein farnesyltransferase as novel anticancer agents. Curr. Top. Med. Chem., 2002, 2, 303-323.
-
(2002)
Curr. Top. Med. Chem
, vol.2
, pp. 303-323
-
-
Ohkanda, J.1
Knowles, D.B.2
Blaskovich, M.A.3
Sebti, S.M.4
Hamilton, A.D.5
-
114
-
-
0029823720
-
Cuprate-mediated synthesis and biological evaluation of cyclopropyl-and tert-butylfarnesyl diphosphate analogs
-
Mu, Y.Q.; Gibbs, R.A.; Eubanks, L.M.; Poulter, C.D. Cuprate-mediated synthesis and biological evaluation of cyclopropyl-and tert-butylfarnesyl diphosphate analogs. J. Org. Chem., 1996, 61, 8010-8015.
-
(1996)
J. Org. Chem
, vol.61
, pp. 8010-8015
-
-
Mu, Y.Q.1
Gibbs, R.A.2
Eubanks, L.M.3
Poulter, C.D.4
-
115
-
-
0028884392
-
A stereoselective palladium copper-catalyzed route to isoprenoids-synthesis and biological evaluation of 13-methylidenefarnesyl diphosphate
-
Gibbs, R.A.; Krishnan, U.; Dolence, J.M.; Poulter, C.D. A stereoselective palladium copper-catalyzed route to isoprenoids-synthesis and biological evaluation of 13-methylidenefarnesyl diphosphate. J. Org. Chem., 1995, 60, 7821-7829.
-
(1995)
J. Org. Chem
, vol.60
, pp. 7821-7829
-
-
Gibbs, R.A.1
Krishnan, U.2
Dolence, J.M.3
Poulter, C.D.4
-
116
-
-
0037026543
-
Synthesis of 7-substituted farnesyl diphosphate analogues
-
Rawat, D.S.; Gibbs, R.A. Synthesis of 7-substituted farnesyl diphosphate analogues. Org. Lett., 2002, 4, 3027-3030.
-
(2002)
Org. Lett
, vol.4
, pp. 3027-3030
-
-
Rawat, D.S.1
Gibbs, R.A.2
-
117
-
-
79960167274
-
New synthetic methodology for the construction of 7-substituted farnesyl diphosphate analogs
-
Placzek, A.T.; Gibbs, R.A. New synthetic methodology for the construction of 7-substituted farnesyl diphosphate analogs. Org. Lett., 2011, 13, 3576-3579.
-
(2011)
Org. Lett
, vol.13
, pp. 3576-3579
-
-
Placzek, A.T.1
Gibbs, R.A.2
-
118
-
-
81355135331
-
Geranylgeranyl diphosphate synthase: An emerging therapeutic target
-
Wiemer, A.J.; Wiemer, D.F.; Hohl, R.J. Geranylgeranyl diphosphate synthase: An emerging therapeutic target. Clin. Pharmacol. Ther., 2011, 90, 804-812.
-
(2011)
Clin. Pharmacol. Ther
, vol.90
, pp. 804-812
-
-
Wiemer, A.J.1
Wiemer, D.F.2
Hohl, R.J.3
-
119
-
-
0003873024
-
-
Chapman & Hall through CRC Press, Version 11.2: Boca Raton, Florida
-
Dictionary of Natural Products, Chapman & Hall through CRC Press, Version 11.2: Boca Raton, Florida, 2003.
-
(2003)
Dictionary of Natural Products
-
-
-
120
-
-
0037161612
-
Inhibition of geranylgeranyl diphosphate synthase by bisphosphonates and diphosphates: A potential route to new bone antiresorption and antiparasitic agents
-
Szabo, C.M.; Matsumura, Y.; Fukura, S.; Martin, M.B.; Sanders, J.M.; Sengupta, S.; Cieslak, J.A.; Loftus, T.C.; Lea, C.R.; Lee, H.J.; Koohang, A.; Coates, R.M.; Sagami, H.; Oldfield, E. Inhibition of geranylgeranyl diphosphate synthase by bisphosphonates and diphosphates: A potential route to new bone antiresorption and antiparasitic agents. J. Med. Chem., 2002, 45, 2185-2196.
-
(2002)
J. Med. Chem
, vol.45
, pp. 2185-2196
-
-
Szabo, C.M.1
Matsumura, Y.2
Fukura, S.3
Martin, M.B.4
Sanders, J.M.5
Sengupta, S.6
Cieslak, J.A.7
Loftus, T.C.8
Lea, C.R.9
Lee, H.J.10
Koohang, A.11
Coates, R.M.12
Sagami, H.13
Oldfield, E.14
-
121
-
-
38049035846
-
Mono-and dialkyl isoprenoid bisphosphonates as geranylgeranyl diphosphate synthase inhibitors
-
Wiemer, A.J.; Yu, J.S.; Lamb, K.M.; Hohl, R.J.; Wiemer, D.F. Mono-and dialkyl isoprenoid bisphosphonates as geranylgeranyl diphosphate synthase inhibitors. Bioorgan. Med. Chem., 2008, 16, 390-399.
-
(2008)
Bioorgan. Med. Chem
, vol.16
, pp. 390-399
-
-
Wiemer, A.J.1
Yu, J.S.2
Lamb, K.M.3
Hohl, R.J.4
Wiemer, D.F.5
-
122
-
-
33646204998
-
Synthesis and biological activity of isoprenoid bisphosphonates
-
Shull, L.W.; Wiemer, A.J.; Hohl, R.J.; Wiemer, D.F. Synthesis and biological activity of isoprenoid bisphosphonates. Bioorg. Med. Chem., 2006, 14, 4130-4136.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 4130-4136
-
-
Shull, L.W.1
Wiemer, A.J.2
Hohl, R.J.3
Wiemer, D.F.4
-
123
-
-
0001125237
-
Synthesis and characterization of aza analog inhibitors of squalene and geranylgeranyl diphosphate synthases
-
Steiger, A.; Pyun, H.J.; Coates, R.M. Synthesis and characterization of aza analog inhibitors of squalene and geranylgeranyl diphosphate synthases. J. Org. Chem., 1992, 57, 3444-3449.
-
(1992)
J. Org. Chem
, vol.57
, pp. 3444-3449
-
-
Steiger, A.1
Pyun, H.J.2
Coates, R.M.3
-
124
-
-
0029966304
-
Protein prenyltransferases
-
Casey, P.J.; Seabra, M.C. Protein prenyltransferases. J. Biol. Chem., 1996, 271, 5289-5292.
-
(1996)
J. Biol. Chem
, vol.271
, pp. 5289-5292
-
-
Casey, P.J.1
Seabra, M.C.2
-
125
-
-
0036191794
-
Coupling of isoprenoid triflates with organoboron nucleophiles: Synthesis and biological evaluation of geranylgeranyl diphosphate analogues
-
Mu, Y.Q.; Eubanks, L.M.; Poulter, C.D.; Gibbs, R.A. Coupling of isoprenoid triflates with organoboron nucleophiles: Synthesis and biological evaluation of geranylgeranyl diphosphate analogues. Bioorg. Med. Chem., 2002, 10, 1207-1219.
-
(2002)
Bioorg. Med. Chem
, vol.10
, pp. 1207-1219
-
-
Mu, Y.Q.1
Eubanks, L.M.2
Poulter, C.D.3
Gibbs, R.A.4
-
126
-
-
0343941596
-
Mechanism of the biosynthesis of squalene from farnesyl pyrophosphate
-
Dewar, M.J.S.; Ruiz, J.M. Mechanism of the biosynthesis of squalene from farnesyl pyrophosphate. Tetrahedron, 1987, 43, 2661-2674.
-
(1987)
Tetrahedron
, vol.43
, pp. 2661-2674
-
-
Dewar, M.J.S.1
Ruiz, J.M.2
-
128
-
-
0015934140
-
Application of claisen rearrangement to synthesis of trans trisubstituted olefinic bonds-synthesis of squalene and insect juvenile-hormone
-
Faulkner, D.J.; Petersen, M.R. Application of claisen rearrangement to synthesis of trans trisubstituted olefinic bonds-synthesis of squalene and insect juvenile-hormone. J. Am. Chem. Soc., 1973, 95, 553-563.
-
(1973)
J. Am. Chem. Soc
, vol.95
, pp. 553-563
-
-
Faulkner, D.J.1
Petersen, M.R.2
-
129
-
-
84870407838
-
Colony organization in the green alga Botryococcus braunii (Race B) is specified by a complex extracellular matrix
-
Weiss, T.L.; Roth, R.; Goodson, C.; Vitha, S.; Black, I.; Azadi, P.; Rusch, J.; Holzenburg, A.; Devarenne, T.P.; Goodenough, U. Colony organization in the green alga Botryococcus braunii (Race B) is specified by a complex extracellular matrix. Eukaryot. Cell., 2012, 11, 1424-1440.
-
(2012)
Eukaryot. Cell
, vol.11
, pp. 1424-1440
-
-
Weiss, T.L.1
Roth, R.2
Goodson, C.3
Vitha, S.4
Black, I.5
Azadi, P.6
Rusch, J.7
Holzenburg, A.8
Devarenne, T.P.9
Goodenough, U.10
-
130
-
-
79960745217
-
Hydrocarbon productivities in different Botryococcus strains: Comparative methods in product quantification
-
Eroglu, E.; Okada, S.; Melis, A. Hydrocarbon productivities in different Botryococcus strains: comparative methods in product quantification. J. Appl. Phycol., 2011, 23, 763-775.
-
(2011)
J. Appl. Phycol
, vol.23
, pp. 763-775
-
-
Eroglu, E.1
Okada, S.2
Melis, A.3
-
131
-
-
84879952721
-
Evaluation of ionic liquids on phototrophic microbes and their use in biofuel extraction and isolation
-
Lovejoy, K.S.; Davis, L.E.; McClellan, L.M.; Lillo, A.M.; Welsh, J.D.; Schmidt, E.N.; Sanders, C.K.; Lou, A.J.; Fox, D.T.; Koppisch, A.T.; Del Sesto, R.E. Evaluation of ionic liquids on phototrophic microbes and their use in biofuel extraction and isolation. J. Appl. Phycol., 2013, 25, 973-981.
-
(2013)
J. Appl. Phycol
, vol.25
, pp. 973-981
-
-
Lovejoy, K.S.1
Davis, L.E.2
McClellan, L.M.3
Lillo, A.M.4
Welsh, J.D.5
Schmidt, E.N.6
Sanders, C.K.7
Lou, A.J.8
Fox, D.T.9
Koppisch, A.T.10
Del, S.R.E.11
-
132
-
-
84858055815
-
Functional identification of triterpene methyltransferases from Botryococcus braunii Race B
-
Niehaus, T.D.; Kinison, S.; Okada, S.; Yeo, Y.S.; Bell, S.A.; Cui, P.; Devarenne, T.P.; Chappell, J. Functional identification of triterpene methyltransferases from Botryococcus braunii Race B. J. Biol. Chem., 2012, 287, 8163-8173.
-
(2012)
J. Biol. Chem
, vol.287
, pp. 8163-8173
-
-
Niehaus, T.D.1
Kinison, S.2
Okada, S.3
Yeo, Y.S.4
Bell, S.A.5
Cui, P.6
Devarenne, T.P.7
Chappell, J.8
-
133
-
-
84988112516
-
Hydrocracking of the oils of Botryococcus braunii to transport fuels
-
Hillen, L.W.; Pollard, G.; Wake, L.V.; White, N. Hydrocracking of the oils of Botryococcus braunii to transport fuels. Biotechnol. Bioeng., 1982, 24, 193-205.
-
(1982)
Biotechnol. Bioeng
, vol.24
, pp. 193-205
-
-
Hillen, L.W.1
Pollard, G.2
Wake, L.V.3
White, N.4
-
134
-
-
84860791937
-
Synthesis of enantioenriched tertiary boronic esters from secondary allylic carbamates. Application to the synthesis of C30 botryococcene
-
Pulis, A.P.; Aggarwal, V.K. Synthesis of enantioenriched tertiary boronic esters from secondary allylic carbamates. Application to the synthesis of C30 botryococcene. J. Am. Chem. Soc., 2012, 134, 7570-7574.
-
(2012)
J. Am. Chem. Soc
, vol.134
, pp. 7570-7574
-
-
Pulis, A.P.1
Aggarwal, V.K.2
-
135
-
-
77953558234
-
Total synthesis of 7, 11-cyclobotryococca-5, 12, 26-triene using an oxidative radical cyclization as a key step
-
Davies, J.J.; Krulle, T.M.; Burton, J.W. Total synthesis of 7, 11-cyclobotryococca-5, 12, 26-triene using an oxidative radical cyclization as a key step. Org. Lett., 2010, 12, 2738-2741.
-
(2010)
Org. Lett
, vol.12
, pp. 2738-2741
-
-
Davies, J.J.1
Krulle, T.M.2
Burton, J.W.3
-
136
-
-
0003139824
-
The total synthesis of 10-(R,S)-C-30 botryococcene and botryococcane and a new synthesis of a general intermediate to the botryococcene family
-
Hird, N.W.; Lee, T.V.; Leigh, A.J.; Maxwell, J.R.; Peakman, T.M. The total synthesis of 10-(R,S)-C-30 botryococcene and botryococcane and a new synthesis of a general intermediate to the botryococcene family. Tetrahedron Lett., 1989, 30, 4867-4870.
-
(1989)
Tetrahedron Lett
, vol.30
, pp. 4867-4870
-
-
Hird, N.W.1
Lee, T.V.2
Leigh, A.J.3
Maxwell, J.R.4
Peakman, T.M.5
-
137
-
-
0038499149
-
Total synthesis of (-)-botryococcene
-
White, J.D.; Reddy, G.N.; Spessard, G.O. Total synthesis of (-)-botryococcene. J. Am. Chem. Soc., 1988, 110, 1624-1626.
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 1624-1626
-
-
White, J.D.1
Reddy, G.N.2
Spessard, G.O.3
-
138
-
-
37049067936
-
Total synthesis of (-)-C-34-botryococcene, the principal triterpenoid hydrocarbon of the freshwater alga Botryococcus braunii
-
White, J.D.; Reddy, G.N.; Spessard, G.O. Total synthesis of (-)-C-34-botryococcene, the principal triterpenoid hydrocarbon of the freshwater alga Botryococcus braunii. J. Chem. Soc. Perk. T 1, 1993, 759-767.
-
(1993)
J. Chem. Soc. Perk. T
, vol.1
, pp. 759-767
-
-
White, J.D.1
Reddy, G.N.2
Spessard, G.O.3
-
139
-
-
84871311815
-
Zeaxanthin protects plant photosynthesis by modulating chlorophyll triplet yield in specific lightharvesting antenna subunits
-
Dall'Osto, L.; Holt, N.E.; Kaligotla, S.; Fuciman, M.; Cazzaniga, S.; Carbonera, D.; Frank, H.A.; Alric, J.; Bassi, R. Zeaxanthin protects plant photosynthesis by modulating chlorophyll triplet yield in specific lightharvesting antenna subunits. J. Biol. Chem., 2012, 287, 41820-41834.
-
(2012)
J. Biol. Chem
, vol.287
, pp. 41820-41834
-
-
Dall'osto, L.1
Holt, N.E.2
Kaligotla, S.3
Fuciman, M.4
Cazzaniga, S.5
Carbonera, D.6
Frank, H.A.7
Alric, J.8
Bassi, R.9
-
140
-
-
84865316619
-
Carotenoid lutein: A promising candidate for pharmaceutical and nutraceutical applications
-
Shegokar, R.; Mitri, K. Carotenoid lutein: a promising candidate for pharmaceutical and nutraceutical applications. J. Diet. Suppl., 2012, 9, 183-210.
-
(2012)
J. Diet. Suppl
, vol.9
, pp. 183-210
-
-
Shegokar, R.1
Mitri, K.2
-
141
-
-
84859136421
-
Role of carotenoid beta-cryptoxanthin in bone homeostasis
-
Yamaguchi, M. Role of carotenoid beta-cryptoxanthin in bone homeostasis. J. Biomed. Sci., 2012, 19.
-
(2012)
Biomed. Sci
, vol.19
-
-
Yamaguchi, M.1
-
142
-
-
0024464691
-
Lycopene as the most efficient biological carotenoid singlet oxygen quencher
-
Di Mascio, P.; Kaiser, S.; Sies, H. Lycopene as the most efficient biological carotenoid singlet oxygen quencher. Arch. Biochem. Biophys., 1989, 274, 532-538.
-
(1989)
Arch. Biochem. Biophys
, vol.274
, pp. 532-538
-
-
Di, M.P.1
Kaiser, S.2
Sies, H.3
-
143
-
-
79959764237
-
A novel and practical synthetic route for the total synthesis of lycopene
-
Shen, R.P.; Jiang, X.Y.; Ye, W.D.; Song, X.H.; Liu, L.; Lao, X.J.; Wu, C.L. A novel and practical synthetic route for the total synthesis of lycopene. Tetrahedron., 2011, 67, 5610-5614.
-
(2011)
Tetrahedron
, vol.67
, pp. 5610-5614
-
-
Shen, R.P.1
Jiang, X.Y.2
Ye, W.D.3
Song, X.H.4
Liu, L.5
Lao, X.J.6
Wu, C.L.7
-
144
-
-
0034775358
-
Lutein, zeaxanthin, and the macular pigment
-
Landrum, J.T.; Bone, R.A. Lutein, zeaxanthin, and the macular pigment. Arch. Biochem. Biophys., 2001, 385, 28-40.
-
(2001)
Arch. Biochem. Biophys
, vol.385
, pp. 28-40
-
-
Landrum, J.T.1
Bone, R.A.2
-
145
-
-
65949087869
-
Total synthesis of (3R,3 ' R,6 ' R)-Lutein and its stereoisomers
-
Khachik, F.; Chang, A.N. Total synthesis of (3R,3 ' R,6 ' R)-Lutein and its stereoisomers. J. Org. Chem., 2009, 74, 3875-3885.
-
(2009)
J. Org. Chem
, vol.74
, pp. 3875-3885
-
-
Khachik, F.1
Chang, A.N.2
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