-
2
-
-
84995178977
-
Biology and biochemistry of reproduction and contraception
-
W. Jöchle Biology and biochemistry of reproduction and contraception Angew. Chem. Int. Ed. Engl. 1 1962 537 549
-
(1962)
Angew. Chem. Int. Ed. Engl.
, vol.1
, pp. 537-549
-
-
Jöchle, W.1
-
3
-
-
24444454197
-
Estafiatin, a new sesquiterpene lactone Isolated from Artemisia mexicana (Willd)
-
F. Sánchez-Viesca, and J. Romo Estafiatin, a new sesquiterpene lactone Isolated from Artemisia mexicana (Willd) Tetrahedron 19 1963 1285 1291
-
(1963)
Tetrahedron
, vol.19
, pp. 1285-1291
-
-
Sánchez-Viesca, F.1
Romo, J.2
-
4
-
-
0001043606
-
Schistosomicidal sesquiterpene lactone from Eremanthus elaeagnus
-
W. Vichnewski, and B. Gilbert Schistosomicidal sesquiterpene lactone from Eremanthus elaeagnus Phytochemistry 11 1972 2563 2566
-
(1972)
Phytochemistry
, vol.11
, pp. 2563-2566
-
-
Vichnewski, W.1
Gilbert, B.2
-
6
-
-
0013690387
-
Absolute stereochemistry of eremanthine, a schistosomicidal sesquiterpene lactone from Eremanthus elaeagnus
-
M. Garcia, A.J.R. Da Silva, P.M. Baker, B. Gilbert, and J.A. Rabi Absolute stereochemistry of eremanthine, a schistosomicidal sesquiterpene lactone from Eremanthus elaeagnus Phytochemistry 15 1976 331 332
-
(1976)
Phytochemistry
, vol.15
, pp. 331-332
-
-
Garcia, M.1
Da Silva, A.J.R.2
Baker, P.M.3
Gilbert, B.4
Rabi, J.A.5
-
7
-
-
23844459839
-
-
M. Bruno, S. Roselli, A. Maggio, R.A. Ruccuglia, K.F. Bastow, and K.H. Lee J. Nat. Prod. 68 2005 1042 1046
-
(2005)
J. Nat. Prod.
, vol.68
, pp. 1042-1046
-
-
Bruno, M.1
Roselli, S.2
Maggio, A.3
Ruccuglia, R.A.4
Bastow, K.F.5
Lee, K.H.6
-
8
-
-
0000057091
-
Studies on the syntheses of biologically active sesquiterpene lactones
-
M. Ando Studies on the syntheses of biologically active sesquiterpene lactones J. Synth. Org. Chem. Jpn. 50 1992 858 874
-
(1992)
J. Synth. Org. Chem. Jpn.
, vol.50
, pp. 858-874
-
-
Ando, M.1
-
9
-
-
45749114065
-
Cancer stem cells: Models, mechanisms and implications for improved treatment
-
J. Zhou, and Y. Zhang Cancer stem cells: models, mechanisms and implications for improved treatment Cell Cycle 7 2008 1360 1370
-
(2008)
Cell Cycle
, vol.7
, pp. 1360-1370
-
-
Zhou, J.1
Zhang, Y.2
-
10
-
-
33749436571
-
Searching for leukemia stem cells - Not yet the end of the road?
-
C.T. Jordan Searching for leukemia stem cells - not yet the end of the road? Cancer Cell 10 2006 253 254
-
(2006)
Cancer Cell
, vol.10
, pp. 253-254
-
-
Jordan, C.T.1
-
11
-
-
65549140597
-
Effects of the sesquiterpene lactone parthenolide on prostate tumor-initiating cells: An integrated molecular profiling approach
-
B.T. Kawasaki, M. Kalathur, and M. Ana Effects of the sesquiterpene lactone parthenolide on prostate tumor-initiating cells: an integrated molecular profiling approach Prostate 69 2009 827 837
-
(2009)
Prostate
, vol.69
, pp. 827-837
-
-
Kawasaki, B.T.1
Kalathur, M.2
Ana, M.3
-
13
-
-
0038472371
-
Study on effect of Cordyceps sinensisand artemisinin in preventing recurrence of lupus nephritis
-
L. Lu Study on effect of Cordyceps sinensisand artemisinin in preventing recurrence of lupus nephritis Chin. J. Integr. Trad. West. Med. 22 2002 169 171
-
(2002)
Chin. J. Integr. Trad. West. Med.
, vol.22
, pp. 169-171
-
-
Lu, L.1
-
14
-
-
39149087695
-
Artesunate combined with vinorelbine plus cisplatin in treatment of advanced non-small cell lung cancer: A randomized controlled trial
-
Z.Y. Zhang Artesunate combined with vinorelbine plus cisplatin in treatment of advanced non-small cell lung cancer: a randomized controlled trial Chin. J. Integr. Med. 6 2008 1 138
-
(2008)
Chin. J. Integr. Med.
, vol.6
, pp. 1-138
-
-
Zhang, Z.Y.1
-
15
-
-
33644672627
-
Artesunate in the treatment of metastatic uveal melanoma- first experiences
-
T.G. Berger, D. Dieckmann, T. Efferth, E.S. Schultz, J. Funk, A. Baur, and G. Schuler Artesunate in the treatment of metastatic uveal melanoma- first experiences Oncol. Rep. 14 2005 1599 1603
-
(2005)
Oncol. Rep.
, vol.14
, pp. 1599-1603
-
-
Berger, T.G.1
Dieckmann, D.2
Efferth, T.3
Schultz, E.S.4
Funk, J.5
Baur, A.6
Schuler, G.7
-
16
-
-
0036975321
-
Case report of a laryngeal squamous cell carcinoma treated with artesunate
-
N.P. Singh, and K.B. Verma Case report of a laryngeal squamous cell carcinoma treated with artesunate Arch. Oncol. 10 2002 279 280
-
(2002)
Arch. Oncol.
, vol.10
, pp. 279-280
-
-
Singh, N.P.1
Verma, K.B.2
-
17
-
-
33750858216
-
Case report of a pituitary macroadenoma treated with artemether
-
N.P. Singh, and V.K. Panwar Case report of a pituitary macroadenoma treated with artemether Integr. Cancer Ther. 5 2006 391 394
-
(2006)
Integr. Cancer Ther.
, vol.5
, pp. 391-394
-
-
Singh, N.P.1
Panwar, V.K.2
-
18
-
-
39649125467
-
An orally bioavailable parthenolide analog selectively eradicates acute myelogenous leukemia stem and progenitor cells
-
M.L. Guzman, R.M. Rossi, S. Neelakantan, X. Li, C.A. Corbett, D.C. Hassane, M.W. Becker, J.M. Bennett, S. Edmund, J.L. Lachowicz, A. Vaughan, C.J. Sweeney, W. Matthews, M. Carroll, J.L. Liesveld, P.A. Crooks, and C.T. Jordan An orally bioavailable parthenolide analog selectively eradicates acute myelogenous leukemia stem and progenitor cells Blood 110 2007 4427 4435
-
(2007)
Blood
, vol.110
, pp. 4427-4435
-
-
Guzman, M.L.1
Rossi, R.M.2
Neelakantan, S.3
Li, X.4
Corbett, C.A.5
Hassane, D.C.6
Becker, M.W.7
Bennett, J.M.8
Edmund, S.9
Lachowicz, J.L.10
Vaughan, A.11
Sweeney, C.J.12
Matthews, W.13
Carroll, M.14
Liesveld, J.L.15
Crooks, P.A.16
Jordan, C.T.17
-
19
-
-
24644432531
-
The SERCA pump as a therapeutic target: Making a "smart bomb" for prostate cancer
-
S.R. Denmeade, and J.T. Isaacs The SERCA pump as a therapeutic target: making a "smart bomb" for prostate cancer Cancer Biol. Ther. 4 2005 14 22
-
(2005)
Cancer Biol. Ther.
, vol.4
, pp. 14-22
-
-
Denmeade, S.R.1
Isaacs, J.T.2
-
20
-
-
65549138953
-
A trojan horse in drug development: Targeting of thapsigargins towards prostate cancer cells
-
S.B. Christensen, D.M. Skytte, S.R. Denmeade, C. Dionne, J.V. Moller, P. Nissen, and J.T. Isaacs A trojan horse in drug development: targeting of thapsigargins towards prostate cancer cells Anticancer Agents Med. Chem. 9 2009 276 294
-
(2009)
Anticancer Agents Med. Chem.
, vol.9
, pp. 276-294
-
-
Christensen, S.B.1
Skytte, D.M.2
Denmeade, S.R.3
Dionne, C.4
Moller, J.V.5
Nissen, P.6
Isaacs, J.T.7
-
21
-
-
33646024956
-
Molecular pharmacology and pharmacogenomics of artemisinin and its derivatives in cancer cells
-
T. Efferth Molecular pharmacology and pharmacogenomics of artemisinin and its derivatives in cancer cells Curr. Drug Targets 7 2006 407 421
-
(2006)
Curr. Drug Targets
, vol.7
, pp. 407-421
-
-
Efferth, T.1
-
22
-
-
58149316208
-
Transferrin receptor-dependent cytotoxicity of artemisinin-transferrin conjugates on prostate cancer cells and induction of apoptosis
-
I. Nakase, B. Gallis, T. Takatani-Nakase, S. Oh, E. Lacoste, N.P. Singh, D.R. Goodlett, S. Tanaka, S. Futaki, H. Lai, and T. Sasaki Transferrin receptor-dependent cytotoxicity of artemisinin-transferrin conjugates on prostate cancer cells and induction of apoptosis Cancer Lett. 274 2009 290 298
-
(2009)
Cancer Lett.
, vol.274
, pp. 290-298
-
-
Nakase, I.1
Gallis, B.2
Takatani-Nakase, T.3
Oh, S.4
Lacoste, E.5
Singh, N.P.6
Goodlett, D.R.7
Tanaka, S.8
Futaki, S.9
Lai, H.10
Sasaki, T.11
-
23
-
-
0031915368
-
Sesquiterpene lactones specifically inhibit activation of NF kappa B by preventing the degradation of i kappa B-alpha and i kappa B-beta
-
S.P. Hehner, M. Heinrich, P.M. Bork, M. Vogt, F. Ratter, V. Lehmann, K. Schulze-Osthoff, W. Droge, and M.L. Schmitz Sesquiterpene lactones specifically inhibit activation of NF kappa B by preventing the degradation of I kappa B-alpha and I kappa B-beta J. Biol. Chem. 273 1998 1288 1297
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 1288-1297
-
-
Hehner, S.P.1
Heinrich, M.2
Bork, P.M.3
Vogt, M.4
Ratter, F.5
Lehmann, V.6
Schulze-Osthoff, K.7
Droge, W.8
Schmitz, M.L.9
-
24
-
-
48449083208
-
Molecular basis of parthenolide-dependent proapoptotic activity in cancer cells
-
B. Pajik, A. Orzechowski, and B. Gajkowska Molecular basis of parthenolide-dependent proapoptotic activity in cancer cells Folia Histochem. Cytobiol. 46 2008 129 135
-
(2008)
Folia Histochem. Cytobiol.
, vol.46
, pp. 129-135
-
-
Pajik, B.1
Orzechowski, A.2
Gajkowska, B.3
-
25
-
-
66449097674
-
Parthenolide promotes the ubiquitination of MDM2 and activates p53 cellular functions
-
Y.N.V. Gopal, E. Chanchorn, and M.W. Van Dyke Parthenolide promotes the ubiquitination of MDM2 and activates p53 cellular functions Mol. Cancer Ther. 8 2009 552 562
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 552-562
-
-
Gopal, Y.N.V.1
Chanchorn, E.2
Van Dyke, M.W.3
-
26
-
-
0035895758
-
Thapsigargin inhibits angiogenesis in the rat isolated aorta: Studies on the role of intracellular calcium pools
-
N. Shukla, N. Freeman, P. Gadsdon, G.D. Angelini, and J.Y. Jeremy Thapsigargin inhibits angiogenesis in the rat isolated aorta: studies on the role of intracellular calcium pools Cardiovasc. Res. 49 2001 681 689
-
(2001)
Cardiovasc. Res.
, vol.49
, pp. 681-689
-
-
Shukla, N.1
Freeman, N.2
Gadsdon, P.3
Angelini, G.D.4
Jeremy, J.Y.5
-
27
-
-
68849116745
-
Pharmacologic mammary carcino sarcoma cells in vitro and prevent osteolytic bone metastasis in vivo
-
A.I. Idris, H. Libouban, H. Nyangoga, E. Landao-Bassonga, D. Chappard, and S.H. Ralston Pharmacologic mammary carcino sarcoma cells in vitro and prevent osteolytic bone metastasis in vivo Mol. Cancer Ther. 8 2009 2339 2347
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 2339-2347
-
-
Idris, A.I.1
Libouban, H.2
Nyangoga, H.3
Landao-Bassonga, E.4
Chappard, D.5
Ralston, S.H.6
-
28
-
-
34447555612
-
Parthenolide specifically depletes histone deacetylase 1 protein and induces cell death through ataxia telangiectasia mutated
-
Y.N.V. Gopal, T. Arora, and M.W. Van Dyke Parthenolide specifically depletes histone deacetylase 1 protein and induces cell death through ataxia telangiectasia mutated Chem. Biol. 14 2007 813 823
-
(2007)
Chem. Biol.
, vol.14
, pp. 813-823
-
-
Gopal, Y.N.V.1
Arora, T.2
Van Dyke, M.W.3
-
29
-
-
65649091667
-
Modulation of DNA methylation by a sesquiterpene lactone parthenolide
-
Z. Liu, S. Liu, Z. Xie, R.E. Pavlovicz, J. Wu, P. Chen, J. Aimiuwu, J. Pang, D. Bhasin, P. Neviani, J.R. Fuchs, C. Plass, P.K. Li, C. Li, T.H. Huang, L.C. Wu, L. Rush, H. Wang, D. Perrotti, G. Marcucci, and K.K. Chan Modulation of DNA methylation by a sesquiterpene lactone parthenolide J. Pharmacol. Exp. Ther. 329 2009 505 514
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.329
, pp. 505-514
-
-
Liu, Z.1
Liu, S.2
Xie, Z.3
Pavlovicz, R.E.4
Wu, J.5
Chen, P.6
Aimiuwu, J.7
Pang, J.8
Bhasin, D.9
Neviani, P.10
Fuchs, J.R.11
Plass, C.12
Li, P.K.13
Li, C.14
Huang, T.H.15
Wu, L.C.16
Rush, L.17
Wang, H.18
Perrotti, D.19
Marcucci, G.20
Chan, K.K.21
more..
-
31
-
-
20044366966
-
Sesquiterpene lactone arglabin influences DNA synthesis in P388 leukemia cells in vivo
-
N.S. Zhangabylov, L.Y. Dederer, L.B. Gorbacheva, S.V. VasilLeva, A.S. Terekhov, and S.M. Adekenov Sesquiterpene lactone arglabin influences DNA synthesis in P388 leukemia cells in vivo Pharm. Chem. J. 38 2004 651
-
(2004)
Pharm. Chem. J.
, vol.38
, pp. 651
-
-
Zhangabylov, N.S.1
Dederer, L.Y.2
Gorbacheva, L.B.3
Vasilleva, S.V.4
Terekhov, A.S.5
Adekenov, S.M.6
-
33
-
-
0036241803
-
Dimeric guaianolides and a fulvenoguaianolide from Artemisia myriantha
-
H.F. Wong, and G.D. Brown Dimeric guaianolides and a fulvenoguaianolide from Artemisia myriantha J. Nat. Prod. 65 2002 481 486
-
(2002)
J. Nat. Prod.
, vol.65
, pp. 481-486
-
-
Wong, H.F.1
Brown, G.D.2
-
34
-
-
0027201128
-
In vitro biological activities of arglabin, a sesquiterpene lactone from the Chinese herb Artemisia myriantha wall
-
C. Bottex-Gauthier, D. Vidal, F. Picot, P. Potier, F. Menichini, and G. Appendino In vitro biological activities of arglabin, a sesquiterpene lactone from the Chinese herb Artemisia myriantha wall Biotech. Ther. 4 1993 77 98
-
(1993)
Biotech. Ther.
, vol.4
, pp. 77-98
-
-
Bottex-Gauthier, C.1
Vidal, D.2
Picot, F.3
Potier, P.4
Menichini, F.5
Appendino, G.6
-
35
-
-
0025781524
-
The stereochemistry of arglabin a cytotoxic guaianolide from Artemisia myriantha
-
G. Appendino, P. Gariboldi, and P. Menichini The stereochemistry of arglabin a cytotoxic guaianolide from Artemisia myriantha Fitoterapia 62 1991 275 276
-
(1991)
Fitoterapia
, vol.62
, pp. 275-276
-
-
Appendino, G.1
Gariboldi, P.2
Menichini, P.3
-
38
-
-
84943921478
-
Studies on the synthesis of sesquiterpene lactones v. total synthesis of arborescin
-
M. Ando, A. Akahane, and K. Takase Studies on the synthesis of sesquiterpene lactones v. total synthesis of arborescin Chem. Lett. 7 1978 727 730
-
(1978)
Chem. Lett.
, vol.7
, pp. 727-730
-
-
Ando, M.1
Akahane, A.2
Takase, K.3
-
39
-
-
0002936955
-
Third Pedler lecture. the life and work of Otto Wallach
-
L. Ruzicka Third Pedler lecture. The life and work of Otto Wallach J. Chem. Soc. (Resumed) 1932 1582 1597
-
(1932)
J. Chem. Soc. (Resumed)
, pp. 1582-1597
-
-
Ruzicka, L.1
-
40
-
-
0000181440
-
The isoprene rule and the biogenesis of terpenic compounds
-
L. Ruzicka The isoprene rule and the biogenesis of terpenic compounds Experientia 9 1953 357 367
-
(1953)
Experientia
, vol.9
, pp. 357-367
-
-
Ruzicka, L.1
-
41
-
-
33947465850
-
β-Hydroxy-β-methyl-δ-valerolactone (Divalonic acid), a new biological factor
-
D.E. Wolf, C.H. Hoffman, P.E. Aldrich, H.R. Skeggs, L.D. Wright, and K. Folkers β-Hydroxy-β-methyl-δ-valerolactone (Divalonic acid), a new biological factor J. Am. Chem. Soc. 78 1956 4499
-
(1956)
J. Am. Chem. Soc.
, vol.78
, pp. 4499
-
-
Wolf, D.E.1
Hoffman, C.H.2
Aldrich, P.E.3
Skeggs, H.R.4
Wright, L.D.5
Folkers, K.6
-
42
-
-
0001534246
-
The utilization of β-hydroxy-β-methyl-δ valerolactone in cholesterol biosynthesis
-
P.A. Tavormina, M.H. Gibbs, and J.W. Huff The utilization of β-hydroxy-β-methyl-δ valerolactone in cholesterol biosynthesis J. Am. Chem. Soc. 78 1956 4498 4499
-
(1956)
J. Am. Chem. Soc.
, vol.78
, pp. 4498-4499
-
-
Tavormina, P.A.1
Gibbs, M.H.2
Huff, J.W.3
-
43
-
-
0003787442
-
-
Longman Scientific & Technical UK
-
J. Mann, J.R.S. Davidson, J.B. Hobbs, D.V. Banthrope, and J.B. Harborne Natural Products: Their Chemistry and Biological Significance 1994 Longman Scientific & Technical UK 291
-
(1994)
Natural Products: Their Chemistry and Biological Significance
, pp. 291
-
-
Mann, J.1
Davidson, J.R.S.2
Hobbs, J.B.3
Banthrope, D.V.4
Harborne, J.B.5
-
46
-
-
0026639957
-
Sterol molecule: Structure, biosynthesis, and function
-
K. Bloch, and K. Bloch Sterol molecule: structure, biosynthesis, and function Steroids 57 1992 378 383
-
(1992)
Steroids
, vol.57
, pp. 378-383
-
-
Bloch, K.1
Bloch, K.2
-
47
-
-
0029922877
-
Glyceraldehyde 3-phosphate and pyruvate as precursors of isoprenic units in an alternative non-mevalonate pathway for terpenoid biosynthesis
-
M. Rohmer, M. Seemann, S. Horbach, S. Bringer-Meyer, and H. Sahm Glyceraldehyde 3-phosphate and pyruvate as precursors of isoprenic units in an alternative non-mevalonate pathway for terpenoid biosynthesis J. Am. Chem. Soc. 118 1996 2564 2566
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 2564-2566
-
-
Rohmer, M.1
Seemann, M.2
Horbach, S.3
Bringer-Meyer, S.4
Sahm, H.5
-
48
-
-
0035999702
-
Biosynthesis of costunolide, dihydro-costunolide, and leucodin. Demonstration of cytochrome P450-catalyzed formation of the lactone ring present in sesquiterpene lactones of chicory
-
J.W. DeKraker, M.C.R. Franssen, M. Joerink, A. deGroot, and H.J. Bouwmeester Biosynthesis of costunolide, dihydro-costunolide, and leucodin. Demonstration of cytochrome P450-catalyzed formation of the lactone ring present in sesquiterpene lactones of chicory Plant Physiol. 129 2002 257 268
-
(2002)
Plant Physiol.
, vol.129
, pp. 257-268
-
-
Dekraker, J.W.1
Franssen, M.C.R.2
Joerink, M.3
Degroot, A.4
Bouwmeester, H.J.5
-
49
-
-
0002058708
-
The Biogenesis and chemistry of sesquiterpene lactones
-
W. Herz, H. Grisebach, G.W. Kirby, Springer Vienna
-
N.H. Fischer, E.J. Olivier, and H.D. Fischer The Biogenesis and chemistry of sesquiterpene lactones W. Herz, H. Grisebach, G.W. Kirby, Fortschritte der Chemie organischer Naturstoffe/Progress in the Chemistry of Organic Natural Products vol. 38 1979 Springer Vienna 47 320
-
(1979)
Fortschritte der Chemie Organischer Naturstoffe/Progress in the Chemistry of Organic Natural Products
, vol.38
, pp. 47-320
-
-
Fischer, N.H.1
Olivier, E.J.2
Fischer, H.D.3
-
52
-
-
0019460951
-
Molecular structure of a cis-decalin-type eudesmanolide and its formation from a guaianolide-1(10)-epoxide
-
N.H. Fischer, Y.F. Wu-Shih, G. Chiari, F.R. Fronczek, and S.F. Watkins Molecular structure of a cis-decalin-type eudesmanolide and its formation from a guaianolide-1(10)-epoxide J. Nat. Prod. 44 1981 104 110
-
(1981)
J. Nat. Prod.
, vol.44
, pp. 104-110
-
-
Fischer, N.H.1
Wu-Shih, Y.F.2
Chiari, G.3
Fronczek, F.R.4
Watkins, S.F.5
-
53
-
-
60849084896
-
Biogenesis of sesquiterpene lactones, pseudoguaianolides from germacranolides: Theoretical study on the reaction mechanism of terminal biogenesis of 8-epiconfertin
-
J.E. Barquera-Lozada, and G. Cuevas Biogenesis of sesquiterpene lactones, pseudoguaianolides from germacranolides: theoretical study on the reaction mechanism of terminal biogenesis of 8-epiconfertin J. Org. Chem. 74 2009 874 883
-
(2009)
J. Org. Chem.
, vol.74
, pp. 874-883
-
-
Barquera-Lozada, J.E.1
Cuevas, G.2
-
54
-
-
0342704152
-
One step transformation of 4α, 5β-epoxygermacranolide into pseudoguaianolide
-
A. Ortega, and E.A. Maldonado One step transformation of 4α, 5β-epoxygermacranolide into pseudoguaianolide Heterocycles 29 1989 635 638
-
(1989)
Heterocycles
, vol.29
, pp. 635-638
-
-
Ortega, A.1
Maldonado, E.A.2
-
55
-
-
2742553225
-
Biomimetic transformation of a guaianolide to a pseudoguaianolide
-
M.J. Bordoloi, R.P. Sharma, and J.C. Sarma Biomimetic transformation of a guaianolide to a pseudoguaianolide Tetrahedron Lett. 27 1986 4633 4634
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 4633-4634
-
-
Bordoloi, M.J.1
Sharma, R.P.2
Sarma, J.C.3
-
56
-
-
34548204750
-
Enantioselective synthesis of arglabin
-
S. Kalidindi, S.W.B. Jeong, A. Schall, R. Bandichhor, B. Nosse, and O. Reiser Enantioselective synthesis of arglabin Angew. Chem. Int. Ed. 46 2007 6361 6363
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 6361-6363
-
-
Kalidindi, S.1
Jeong, S.W.B.2
Schall, A.3
Bandichhor, R.4
Nosse, B.5
Reiser, O.6
-
57
-
-
84865256244
-
-
Z. Jia-Dai, L. Dongmei, L. Jing, Z. Hao-Liang, L. Jian-Ping, Q. Chuan-Jiang, Z. Quan, and C. Yue J. Org. Chem. 77 2012 7103 7107
-
(2012)
J. Org. Chem.
, vol.77
, pp. 7103-7107
-
-
Jia-Dai, Z.1
Dongmei, L.2
Jing, L.3
Hao-Liang, Z.4
Jian-Ping, L.5
Chuan-Jiang, Q.6
Quan, Z.7
Yue, C.8
-
58
-
-
84925492198
-
Hemisynthesis of a naturally occurring and clinically significant antitumor arglabin from ludartin
-
S.H. Lone, and K.A. Bhat Hemisynthesis of a naturally occurring and clinically significant antitumor arglabin from ludartin Tetrahedron Lett. 56 2015 1908 1910
-
(2015)
Tetrahedron Lett.
, vol.56
, pp. 1908-1910
-
-
Lone, S.H.1
Bhat, K.A.2
-
59
-
-
0141516214
-
Facile asymmetric synthesis of the core nuclei of xanthanolides, guaianolides, and eudesmanolides
-
B. Nosse, R.B. Chhor, W.B. Jeong, C. Boehm, and O. Reiser Facile asymmetric synthesis of the core nuclei of xanthanolides, guaianolides, and eudesmanolides Org. Lett. 5 2003 941 944
-
(2003)
Org. Lett.
, vol.5
, pp. 941-944
-
-
Nosse, B.1
Chhor, R.B.2
Jeong, W.B.3
Boehm, C.4
Reiser, O.5
-
60
-
-
85026880749
-
(+)-(R,R)-Bis(4-isopropyloxazoline) [4R,4R′)-2,2′-(2,2′propanediyl)bis(4-isopropyl-4,5-dihydrooxazole)]
-
D.A. Evans, K.A. Woerpel, B. Nosse, A. Schall, Y. Shinde, E. Jezek, M.M. Haque, R.B. Chhor, O. Reiser, P. Wipf, and N. Jayasuriya (+)-(R,R)-Bis(4-isopropyloxazoline) [4R,4R′)-2,2′-(2,2′propanediyl)bis(4-isopropyl-4,5-dihydrooxazole)] Org. Synth. 83 2006 97
-
(2006)
Org. Synth.
, vol.83
, pp. 97
-
-
Evans, D.A.1
Woerpel, K.A.2
Nosse, B.3
Schall, A.4
Shinde, Y.5
Jezek, E.6
Haque, M.M.7
Chhor, R.B.8
Reiser, O.9
Wipf, P.10
Jayasuriya, N.11
-
61
-
-
17144399175
-
Radical cyclizations as key step for the stereoselective synthesis of Bi- and tricyclic sesquiterpene lactones
-
E. Jezek, A. Schall, P. Kreitmeier, and O. Reiser Radical cyclizations as key step for the stereoselective synthesis of Bi- and tricyclic sesquiterpene lactones Synlett 2005 915 918
-
(2005)
Synlett
, pp. 915-918
-
-
Jezek, E.1
Schall, A.2
Kreitmeier, P.3
Reiser, O.4
-
62
-
-
0031562097
-
The preparation of optically active 2-cyclopenten-1,4-diol derivatives from furfuryl alcohol
-
T.T. Curran, D.A. Hay, C.P. Koegel, and J.C. Evans The preparation of optically active 2-cyclopenten-1,4-diol derivatives from furfuryl alcohol Tetrahedron 53 1997 1983 2004
-
(1997)
Tetrahedron
, vol.53
, pp. 1983-2004
-
-
Curran, T.T.1
Hay, D.A.2
Koegel, C.P.3
Evans, J.C.4
-
63
-
-
85077897850
-
-
T. Hayashi, T. Fujiwa, Y. Okamoto, Y. Katsuro, and M. Kumada Cross Coupling of Enol Phosphates with Trimethylsilyl Methylmagnesium Halides Catalyzed by Nickel or Palladium Complexes; A Selective Synthesis of Allylsilanes Synthesis 1981 1001 1003
-
(1981)
Cross Coupling of Enol Phosphates with Trimethylsilyl Methylmagnesium Halides Catalyzed by Nickel or Palladium Complexes; A Selective Synthesis of Allylsilanes Synthesis
, pp. 1001-1003
-
-
Hayashi, T.1
Fujiwa, T.2
Okamoto, Y.3
Katsuro, Y.4
Kumada, M.5
-
64
-
-
0000458209
-
Substrate-directable chemical reactions
-
A.H. Hoveyda, D.A. Evans, and G.C. Fu Substrate-directable chemical reactions Chem. Rev. 93 1993 1307 1370
-
(1993)
Chem. Rev.
, vol.93
, pp. 1307-1370
-
-
Hoveyda, A.H.1
Evans, D.A.2
Fu, G.C.3
-
65
-
-
37049058840
-
Aspects of stereochemistry. Part I. Stereospecificity in formation of epoxides from cyclic allylic alcohols
-
H.B. Henbest Aspects of stereochemistry. Part I. Stereospecificity in formation of epoxides from cyclic allylic alcohols J. Chem. Soc. 1957 1958 1965
-
(1957)
J. Chem. Soc.
, pp. 1958-1965
-
-
Henbest, H.B.1
-
67
-
-
0037375657
-
Parthenolide and its photochemically synthesized 1(10)Z isomer: Chemical reactivity and structure-activity relationship studies in human leucocyte chemotaxis
-
H. Neukirch, N.C. Kaneider, C.J. Wiedermann, A. Guerriero, and M. D'Ambrosio Parthenolide and its photochemically synthesized 1(10)Z isomer: chemical reactivity and structure-activity relationship studies in human leucocyte chemotaxis Bioorg. Med. Chem. 11 2003 1503 1510
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 1503-1510
-
-
Neukirch, H.1
Kaneider, N.C.2
Wiedermann, C.J.3
Guerriero, A.4
D'Ambrosio, M.5
-
69
-
-
0000497219
-
Anticancer sesquiterpene lactones of Michelia compressa (magnoliaceae)
-
M. Ogura, G.A. Cordell, and N.R. Farnsworth Anticancer sesquiterpene lactones of Michelia compressa (magnoliaceae) Phytochemistry 17 1978 957 961
-
(1978)
Phytochemistry
, vol.17
, pp. 957-961
-
-
Ogura, M.1
Cordell, G.A.2
Farnsworth, N.R.3
-
71
-
-
0026099388
-
Synthesis of a ring a precursor of doxorubicin: Stereoselective control of the epoxidation of a homoallylic alcohol by hydroxyl and ester groups
-
T. Chamberlain, X. Fu, J.T. Pechacek, X. Peng, D.M.S. Wheeler, and M.M. Wheeler Synthesis of a ring a precursor of doxorubicin: stereoselective control of the epoxidation of a homoallylic alcohol by hydroxyl and ester groups Tetrahedron Lett. 32 1991 1707 1710
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 1707-1710
-
-
Chamberlain, T.1
Fu, X.2
Pechacek, J.T.3
Peng, X.4
Wheeler, D.M.S.5
Wheeler, M.M.6
-
72
-
-
0001904567
-
Asymmetric epoxidation of homoallylic alcohols using zirconium tetrapropoxide, dicyclohexyltartramide, and t-butyl hydro peroxide system
-
S. Ikegami, T. Katsuki, and M. Yamaguchi Asymmetric epoxidation of homoallylic alcohols using zirconium tetrapropoxide, dicyclohexyltartramide, and t-butyl hydro peroxide system Chem. Lett. 16 1987 83 84
-
(1987)
Chem. Lett.
, vol.16
, pp. 83-84
-
-
Ikegami, S.1
Katsuki, T.2
Yamaguchi, M.3
-
73
-
-
37049079765
-
Stereochemistry of epoxidation of allylic and homoallylic cyclohexene alcohols
-
P. Kocovsky Stereochemistry of epoxidation of allylic and homoallylic cyclohexene alcohols J. Chem. Soc. Perkin Trans. 1 1 1994 1759 1763
-
(1994)
J. Chem. Soc. Perkin Trans. 1
, vol.1
, pp. 1759-1763
-
-
Kocovsky, P.1
-
75
-
-
0000331564
-
The reactions of an N-sulfonylamine inner salt
-
G.M. Atkins, and E.M. Burgess The reactions of an N-sulfonylamine inner salt J. Am. Chem. Soc. 90 1968 4744 4745
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 4744-4745
-
-
Atkins, G.M.1
Burgess, E.M.2
-
76
-
-
48649109292
-
Anti-HBV agents. Part 1: Synthesis of alisol A derivatives: A new class of hepatitis B virus inhibitors
-
Q. Zhang, Z.Y. Jiang, J. Luo, P. Cheng, Y.B. Ma, X.M. Zhang, F.X. Zhang, J. Zhou, and J.J. Chen Anti-HBV agents. Part 1: Synthesis of alisol A derivatives: A new class of hepatitis B virus inhibitors Bioorg. Med. Chem. Lett. 18 2008 4647 4650
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 4647-4650
-
-
Zhang, Q.1
Jiang, Z.Y.2
Luo, J.3
Cheng, P.4
Ma, Y.B.5
Zhang, X.M.6
Zhang, F.X.7
Zhou, J.8
Chen, J.J.9
-
78
-
-
33947088667
-
Sulfuranes. VI. Reactions involving the alkoxy ligands of dialkoxydiarylsulfuranes. Formation of olefins and ethers
-
R.J. Arhart, and J.C. Martin Sulfuranes. VI. Reactions involving the alkoxy ligands of dialkoxydiarylsulfuranes. Formation of olefins and ethers J. Am. Chem. Soc. 94 1972 5003 5010
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 5003-5010
-
-
Arhart, R.J.1
Martin, J.C.2
-
79
-
-
0038200876
-
Studies on the syntheses of sesquiterpene lactones. 15. Synthesis of four possible diastereoisomers of Bohlmann's structure of isoepoxyestafiatin. the stereochemical assignment of isoepoxyestafiatin
-
M. Ando, and H. Yoshimura Studies on the syntheses of sesquiterpene lactones. 15. Synthesis of four possible diastereoisomers of Bohlmann's structure of isoepoxyestafiatin. The stereochemical assignment of isoepoxyestafiatin J. Org. Chem. 58 1993 4127 4131
-
(1993)
J. Org. Chem.
, vol.58
, pp. 4127-4131
-
-
Ando, M.1
Yoshimura, H.2
-
80
-
-
84886424782
-
Isolation, cytotoxicity evaluation and HPLC quantification of the chemical constituents from Artemisia amygdalina Decne
-
S.H. Lone, K.A. Bhat, Syed Naseer, R.A. Rather, M.A. Khuroo, and S.A. Tasduq Isolation, cytotoxicity evaluation and HPLC quantification of the chemical constituents from Artemisia amygdalina Decne J. Chromatogr. B 940 2013 135 141
-
(2013)
J. Chromatogr. B
, vol.940
, pp. 135-141
-
-
Lone, S.H.1
Bhat, K.A.2
Naseer, S.3
Rather, R.A.4
Khuroo, M.A.5
Tasduq, S.A.6
-
81
-
-
84881375742
-
Synthesis and biological evaluation of amino analogs of Ludartin: Potent and selective cytotoxic agents
-
S.H. Lone, K.A. Bhat, Shakeel-u-Rehman, R. Majeed, A. Hamid, and M.A. Khuroo Synthesis and biological evaluation of amino analogs of Ludartin: potent and selective cytotoxic agents Bioorg. Med. Chem. Lett. 23 2013 4931 4934
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 4931-4934
-
-
Lone, S.H.1
Bhat, K.A.2
Shakeel-U-Rehman3
Majeed, R.4
Hamid, A.5
Khuroo, M.A.6
-
82
-
-
84893723977
-
Click chemistry inspired facile synthesis and bioevaluation of novel triazolyl analogs of Ludartin
-
S.H. Lone, K.A. Bhat, R. Majeed, A. Hamid, and M.A. Khuroo Click chemistry inspired facile synthesis and bioevaluation of novel triazolyl analogs of Ludartin Bioorg. Med. Chem. Lett. 24 2014 1047 1051
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 1047-1051
-
-
Lone, S.H.1
Bhat, K.A.2
Majeed, R.3
Hamid, A.4
Khuroo, M.A.5
-
83
-
-
34249915980
-
Reactions at the double bond in the epoxy group of arglabin
-
S.M. Adekenov, K.A. Aituganov, K.M. Turdybekov, S.V. Lindeman, Y.T. Struchkov, I.Y. Bagryanskaya, and Y.V. Gatilov Reactions at the double bond in the epoxy group of arglabin Khimiya Prir. Soedin. 1 1991 27 35
-
(1991)
Khimiya Prir. Soedin.
, vol.1
, pp. 27-35
-
-
Adekenov, S.M.1
Aituganov, K.A.2
Turdybekov, K.M.3
Lindeman, S.V.4
Struchkov, Y.T.5
Bagryanskaya, I.Y.6
Gatilov, Y.V.7
-
84
-
-
0038323224
-
First synthesis of dialkyl phosphonate derivatives of sesquiterpene α- Methylene-γ-lactone
-
R.I. Jalmahanbetova, B.B. Rakhimova, V.A. Raldugin, I.Y. Bagryanskaya, Y.V. Gatilov, V. Yu, M.M. Shakirov, A.T. Kulyjasov, S.M. Adekenov, and G.A. Tolstikov First synthesis of dialkyl phosphonate derivatives of sesquiterpene α- methylene-γ-lactone Russ. Chem. Bull. 52 2003 748 751
-
(2003)
Russ. Chem. Bull.
, vol.52
, pp. 748-751
-
-
Jalmahanbetova, R.I.1
Rakhimova, B.B.2
Raldugin, V.A.3
Bagryanskaya, I.Y.4
Gatilov, Y.V.5
Yu, V.6
Shakirov, M.M.7
Kulyjasov, A.T.8
Adekenov, S.M.9
Tolstikov, G.A.10
-
85
-
-
38049141695
-
Preparation and structure elucidation of two minor products from reaction of arglabin with chloroform in the presence of a crown ether
-
R.I. Jalmakhanbetova, G.A. Atazhanova, V.A. Raldugin, Y.I. Bagryanskaya, Y.V. Gatilov, M.M. Shakirov, and S.M. Adekenov Preparation and structure elucidation of two minor products from reaction of arglabin with chloroform in the presence of a crown ether Chem. Nat. Compd. 43 2007 548 551
-
(2007)
Chem. Nat. Compd.
, vol.43
, pp. 548-551
-
-
Jalmakhanbetova, R.I.1
Atazhanova, G.A.2
Raldugin, V.A.3
Bagryanskaya, Y.I.4
Gatilov, Y.V.5
Shakirov, M.M.6
Adekenov, S.M.7
-
86
-
-
30544455291
-
-
R.I. Jalmakhanbetova, V.A. Raldugin, I.Y. Bagryanskaya, Y.V. Gatilov, M.M. Shakirov, A.T. Kulyyasov, and S.M. Adekenov Chem. Nat. Compd. 41 2005 552 555
-
(2005)
Chem. Nat. Compd.
, vol.41
, pp. 552-555
-
-
Jalmakhanbetova, R.I.1
Raldugin, V.A.2
Bagryanskaya, I.Y.3
Gatilov, Y.V.4
Shakirov, M.M.5
Kulyyasov, A.T.6
Adekenov, S.M.7
-
87
-
-
84858016984
-
Synthesis and biological evaluation of antitumor-active arglabin derivatives
-
R. Csuk, A. Heinold, B. Siewert, S. Schwarz, A. Barthel, R. Kluge, and D. Strohl Synthesis and biological evaluation of antitumor-active arglabin derivatives Arch. Pharm. Chem. Life Sci. 000 2012 1 8
-
(2012)
Arch. Pharm. Chem. Life Sci.
, pp. 1-8
-
-
Csuk, R.1
Heinold, A.2
Siewert, B.3
Schwarz, S.4
Barthel, A.5
Kluge, R.6
Strohl, D.7
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