-
1
-
-
84886597091
-
Synthesis and biological testing of steroid derivatives as inhibitors
-
D. Poirier Synthesis and biological testing of steroid derivatives as inhibitors J. Steroid Biochem. Mol. Biol. 137 2013 174 175
-
(2013)
J. Steroid Biochem. Mol. Biol.
, vol.137
, pp. 174-175
-
-
Poirier, D.1
-
2
-
-
84874656763
-
An overview of synthetic approaches for heterocyclic steroids
-
R. Singh, and G. Panda An overview of synthetic approaches for heterocyclic steroids Tetrahedron 69 2013 2853 2884
-
(2013)
Tetrahedron
, vol.69
, pp. 2853-2884
-
-
Singh, R.1
Panda, G.2
-
3
-
-
84872528200
-
Rapid microwave assisted synthesis and antimicrobial bioevaluation of novel steroidal chalcones
-
D. Kakati, R.K. Sarma, R. Saikia, N.C. Barua, and J.C. Sarma Rapid microwave assisted synthesis and antimicrobial bioevaluation of novel steroidal chalcones Steroids 78 2013 321 326
-
(2013)
Steroids
, vol.78
, pp. 321-326
-
-
Kakati, D.1
Sarma, R.K.2
Saikia, R.3
Barua, N.C.4
Sarma, J.C.5
-
4
-
-
84884780752
-
Stereoselective synthesis of novel antiproliferative steroidal (E,E) dienamides through a cascade aldol/cyclization process
-
B. Yu, X.N. Yu, X.J. Shi, P.P. Qi, Y. Fang, E. Zhang, D.Q. Yu, and H.M. Liu Stereoselective synthesis of novel antiproliferative steroidal (E,E) dienamides through a cascade aldol/cyclization process Steroids 78 2013 1134 1140
-
(2013)
Steroids
, vol.78
, pp. 1134-1140
-
-
Yu, B.1
Yu, X.N.2
Shi, X.J.3
Qi, P.P.4
Fang, Y.5
Zhang, E.6
Yu, D.Q.7
Liu, H.M.8
-
5
-
-
0000097162
-
Dimeric and oligomeric steroids
-
Y. Li, and J.R. Dias Dimeric and oligomeric steroids Chem. Rev. 97 1997 283 304 (Pubitemid 127662447)
-
(1997)
Chemical Reviews
, vol.97
, Issue.1
, pp. 283-304
-
-
Li, Y.1
Dias, J.R.2
-
6
-
-
34248545237
-
A review on synthetic and natural steroid dimers: 1997-2006
-
DOI 10.2174/092986707780597880
-
L. Nahar, S.D. Sarker, and A.B. Turner A review on synthetic and natural steroid dimers: 1997-2006 Curr. Med. Chem. 14 2007 1349 1370 (Pubitemid 46746365)
-
(2007)
Current Medicinal Chemistry
, vol.14
, Issue.12
, pp. 1349-1370
-
-
Nahar, L.1
Sarker, S.D.2
Turner, A.B.3
-
7
-
-
0026490389
-
Synthesis and pharmacological evaluation of nonacyclic and trisdecacyclic pyrazines related to cephalostatin
-
Y. Pan, R.L. Merriman, L.R. Tanzer, and P.L. Fuchs Synthesis and pharmacological evaluation of nonacyclic and trisdecacyclic pyrazines related to cephalostatin Bioorg. Med. Chem. Lett. 2 1992 967 972
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 967-972
-
-
Pan, Y.1
Merriman, R.L.2
Tanzer, L.R.3
Fuchs, P.L.4
-
8
-
-
84884373879
-
A novel [1,2,4] triazolo [1,5-A] pyrimidine-based phenyl-linked steroid dimer: Synthesis and its cytotoxic activity
-
B. Yu, X.J. Shi, Y.F. Zheng, Y. Fang, E. Zhang, D.Q. Yu, and H.M. Liu A novel [1,2,4] triazolo [1,5-a] pyrimidine-based phenyl-linked steroid dimer: synthesis and its cytotoxic activity Eur. J. Med. Chem. 69 2013 323 330
-
(2013)
Eur. J. Med. Chem.
, vol.69
, pp. 323-330
-
-
Yu, B.1
Shi, X.J.2
Zheng, Y.F.3
Fang, Y.4
Zhang, E.5
Yu, D.Q.6
Liu, H.M.7
-
9
-
-
0034710713
-
Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: Structure and antimalarial and antiproliferative activity
-
D. Opsenica, G. Pocsfalvi, Z. Juranić, B. Tinant, J.P. Declercq, D.E. Kyle, W.K. Milhous, and B.A. Šolaja Cholic acid derivatives as 1,2,4,5-tetraoxane carriers: structure and antimalarial and antiproliferative activity J. Med. Chem. 43 2000 3274 3282
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3274-3282
-
-
Opsenica, D.1
Pocsfalvi, G.2
Juranić, Z.3
Tinant, B.4
Declercq, J.P.5
Kyle, D.E.6
Milhous, W.K.7
Šolaja, B.A.8
-
10
-
-
77950493758
-
Natural products and their biological targets: Proteomic and metabolomic labeling strategies
-
T. Böttcher, M. Pitscheider, and S.A. Sieber Natural products and their biological targets: proteomic and metabolomic labeling strategies Angew. Chem. Int. Ed. 49 2010 2680 2698
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 2680-2698
-
-
Böttcher, T.1
Pitscheider, M.2
Sieber, S.A.3
-
11
-
-
84874638172
-
Selective tumor cell targeting by the disaccharide moiety of bleomycin
-
Z. Yu, R.M. Schmaltz, T.C. Bozeman, R. Paul, M.J. Rishel, K.S. Tsosie, and S.M. Hecht Selective tumor cell targeting by the disaccharide moiety of bleomycin J. Am. Chem. Soc. 135 2013 2883 2886
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 2883-2886
-
-
Yu, Z.1
Schmaltz, R.M.2
Bozeman, T.C.3
Paul, R.4
Rishel, M.J.5
Tsosie, K.S.6
Hecht, S.M.7
-
12
-
-
0036679630
-
Modern methods to produce natural-product libraries
-
DOI 10.1016/S1367-5931(02)00338-1
-
U. Abel, C. Koch, M. Speitling, and F.G. Hansske Modern methods to produce natural-product libraries Curr. Opin. Chem. Biol. 6 2002 453 458 (Pubitemid 34804767)
-
(2002)
Current Opinion in Chemical Biology
, vol.6
, Issue.4
, pp. 453-458
-
-
Abel, U.1
Koch, C.2
Speitling, M.3
Hansske, F.G.4
-
13
-
-
36749025633
-
Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
-
DOI 10.1002/anie.200701342
-
C.V. Galliford, and K.A. Scheidt Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents Angew. Chem. Int. Ed. 46 2007 8748 8758 (Pubitemid 350207923)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.46
, pp. 8748-8758
-
-
Galliford, C.V.1
Scheidt, K.A.2
-
14
-
-
33745154819
-
Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction
-
DOI 10.1021/jm051122a
-
K. Ding, Y. Lu, Z. Nikolovska-Coleska, G. Wang, S. Qiu, S. Shangary, W. Gao, D. Qin, J. Stuckey, K. Krajewski, P.P. Roller, and S. Wang Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction J. Med. Chem. 49 2006 3432 3435 (Pubitemid 43902447)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.12
, pp. 3432-3435
-
-
Ding, K.1
Lu, Y.2
Nikolovska-Coleska, Z.3
Wang, G.4
Qiu, S.5
Shangary, S.6
Gao, W.7
Qin, D.8
Stuckey, J.9
Krajewski, K.10
Roller, P.P.11
Wang, S.12
-
15
-
-
77956280420
-
Spiroindolones, a potent compound class for the treatment of malaria
-
M. Rottmann, C. McNamara, B.K. Yeung, M.C. Lee, B. Zou, B. Russell, P. Seitz, D.M. Plouffe, N.V. Dharia, J. Tan, S.B. Cohen, K.R. Spencer, G.E. Gonzalez-Paez, S.B. Lakshminarayana, A. Goh, R. Suwanarusk, T. Jegla, E.K. Schmitt, H.P. Beck, R. Brun, F. Nosten, L. Renia, V. Dartois, T.H. Keller, D.A. Fidock, E.A. Winzeler, and T.T. Diagana Spiroindolones, a potent compound class for the treatment of malaria Science 329 2010 1175 1180
-
(2010)
Science
, vol.329
, pp. 1175-1180
-
-
Rottmann, M.1
McNamara, C.2
Yeung, B.K.3
Lee, M.C.4
Zou, B.5
Russell, B.6
Seitz, P.7
Plouffe, D.M.8
Dharia, N.V.9
Tan, J.10
Cohen, S.B.11
Spencer, K.R.12
Gonzalez-Paez, G.E.13
Lakshminarayana, S.B.14
Goh, A.15
Suwanarusk, R.16
Jegla, T.17
Schmitt, E.K.18
Beck, H.P.19
Brun, R.20
Nosten, F.21
Renia, L.22
Dartois, V.23
Keller, T.H.24
Fidock, D.A.25
Winzeler, E.A.26
Diagana, T.T.27
more..
-
16
-
-
22944473048
-
Structure-based design of potent non-peptide MDM2 inhibitors
-
DOI 10.1021/ja051147z
-
K. Ding, Y. Lu, Z. Nikolovska-Coleska, S. Qiu, Y. Ding, W. Gao, J. Stuckey, K. Krajewski, P.P. Roller, Y. Tomita, D.A. Parrish, J.R. Deschamps, and S. Wang Structure-based design of potent non-peptide MDM2 inhibitors J. Am. Chem. Soc. 127 2005 10130 10131 (Pubitemid 41045454)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.29
, pp. 10130-10131
-
-
Ding, K.1
Lu, Y.2
Nikolovska-Coleska, Z.3
Qiu, S.4
Ding, Y.5
Gao, W.6
Stuckey, J.7
Krajewski, K.8
Roller, P.P.9
Tomita, Y.10
Parrish, D.A.11
Deschamps, J.R.12
Wang, S.13
-
17
-
-
84860300994
-
Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity
-
G. Bhaskar, Y. Arun, C. Balachandran, C. Saikumar, and P.T. Perumal Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity Eur. J. Med. Chem. 51 2012 79 91
-
(2012)
Eur. J. Med. Chem.
, vol.51
, pp. 79-91
-
-
Bhaskar, G.1
Arun, Y.2
Balachandran, C.3
Saikumar, C.4
Perumal, P.T.5
-
18
-
-
84875229746
-
Synthesis and discovery of novel piperidone-grafted mono- and bis-spirooxindole-hexahydropyrrolizines as potent cholinesterase inhibitors
-
Y. kia, H. Osman, R.S. Kumar, V. Murugaiyah, A. Basiri, S. Perumal, H.A. Wahab, and C.S. Bing Synthesis and discovery of novel piperidone-grafted mono- and bis-spirooxindole-hexahydropyrrolizines as potent cholinesterase inhibitors Bioorg. Med. Chem. 21 2013 1696 1707
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 1696-1707
-
-
Kia, Y.1
Osman, H.2
Kumar, R.S.3
Murugaiyah, V.4
Basiri, A.5
Perumal, S.6
Wahab, H.A.7
Bing, C.S.8
-
19
-
-
81255211335
-
Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles
-
J. Yu, F. Shi, and L.-Z. Gong Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles Acc. Chem. Res. 44 2011 1156 1171
-
(2011)
Acc. Chem. Res.
, vol.44
, pp. 1156-1171
-
-
Yu, J.1
Shi, F.2
Gong, L.-Z.3
-
20
-
-
0037165823
-
2 receptors expressed in Xenopus oocyte
-
DOI 10.1016/S0014-2999(02)01608-4, PII S0014299902016084
-
T.-H. Kang, K. Matsumoto, M. Tohda, Y. Murakami, H. Takayama, M. Kitajima, N. Aimi, and H. Watanabe Pteropodine and isopteropodine positively modulate the function of rat muscarinic M1 and 5-HT2 receptors expressed in Xenopus oocyte Eur. J. Pharmacol. 444 2002 39 45 (Pubitemid 34621332)
-
(2002)
European Journal of Pharmacology
, vol.444
, Issue.1-2
, pp. 39-45
-
-
Kang, T.-H.1
Matsumoto, K.2
Tohda, M.3
Murakami, Y.4
Takayama, H.5
Kitajima, M.6
Aimi, N.7
Watanabe, H.8
-
21
-
-
77953129713
-
Design and synthesis of spirotryprostatin-inspired diketopiperazine systems from prolyl spirooxoindolethiazolidine derivatives
-
A. Bertamino, C. Aquino, M. Sala, N.d. Simone, C.A. Mattia, L. Erra, S. Musella, P. Iannelli, A. Carotenuto, P. Grieco, E. Novellino, P. Campiglia, and I. Gomez-Monterrey Design and synthesis of spirotryprostatin-inspired diketopiperazine systems from prolyl spirooxoindolethiazolidine derivatives Bioorg. Med. Chem. 18 2010 4328 4337
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 4328-4337
-
-
Bertamino, A.1
Aquino, C.2
Sala, M.3
Simone, N.D.4
Mattia, C.A.5
Erra, L.6
Musella, S.7
Iannelli, P.8
Carotenuto, A.9
Grieco, P.10
Novellino, E.11
Campiglia, P.12
Gomez-Monterrey, I.13
-
22
-
-
84875191834
-
Facile synthesis of novel D-ring modified steroidal dienamides via rearrangement of 2H-pyrans
-
B. Yu, E. Zhang, X.N. Sun, J.L. Ren, Y. Fang, B.L. Zhang, D.Q. Yu, and H.M. Liu Facile synthesis of novel D-ring modified steroidal dienamides via rearrangement of 2H-pyrans Steroids 78 2013 494 499
-
(2013)
Steroids
, vol.78
, pp. 494-499
-
-
Yu, B.1
Zhang, E.2
Sun, X.N.3
Ren, J.L.4
Fang, Y.5
Zhang, B.L.6
Yu, D.Q.7
Liu, H.M.8
-
23
-
-
84879209332
-
Efficient construction of novel D-ring modified steroidal dienamides and their cytotoxic activities
-
B. Yu, X.-J. Shi, J.-l. Ren, X.-N. Sun, P.-P. Qi, Y. Fang, X.-W. Ye, M.-M. Wang, J.-W. Wang, E. Zhang, D.-Q. Yu, and H.-M. Liu Efficient construction of novel D-ring modified steroidal dienamides and their cytotoxic activities Eur. J. Med. Chem. 66 2013 171 179
-
(2013)
Eur. J. Med. Chem.
, vol.66
, pp. 171-179
-
-
Yu, B.1
Shi, X.-J.2
Sun, X.-N.3
Qi, P.-P.4
Fang, Y.5
Ye, X.-W.6
Wang, M.-M.7
Wang, J.-W.8
Zhang, E.9
Yu, D.-Q.10
Liu, H.-M.11
-
24
-
-
84876593078
-
Isocyanide-based multicomponent reactions: Catalyst-free stereoselective construction of polycyclic spiroindolines
-
X. Wang, S.-Y. Wang, and S.-J. Ji Isocyanide-based multicomponent reactions: catalyst-free stereoselective construction of polycyclic spiroindolines Org. Lett. 15 2013 1954 1957
-
(2013)
Org. Lett.
, vol.15
, pp. 1954-1957
-
-
Wang, X.1
Wang, S.-Y.2
Ji, S.-J.3
-
25
-
-
79957462689
-
Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst
-
B. Tan, N.R. Candeias, and C.F. Barbas Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst Nature Chem. 3 2011 473 477
-
(2011)
Nature Chem.
, vol.3
, pp. 473-477
-
-
Tan, B.1
Candeias, N.R.2
Barbas, C.F.3
-
26
-
-
84873313546
-
Three-component stereoselective synthesis of spirooxindole derivatives
-
F. Yu, R. Huang, H. Ni, J. Fan, S. Yan, and J. Lin Three-component stereoselective synthesis of spirooxindole derivatives Green Chem. 15 2013 453 462
-
(2013)
Green Chem.
, vol.15
, pp. 453-462
-
-
Yu, F.1
Huang, R.2
Ni, H.3
Fan, J.4
Yan, S.5
Lin, J.6
-
27
-
-
84876530424
-
Efficient construction of highly functionalized spiro[gamma- butyrolactone-pyrrolidin-3,3′-oxindole] tricyclic skeletons via an organocatalytic 1,3-dipolar cycloaddition
-
L. Wang, X.M. Shi, W.P. Dong, L.P. Zhu, and R. Wang Efficient construction of highly functionalized spiro[gamma-butyrolactone-pyrrolidin-3, 3′-oxindole] tricyclic skeletons via an organocatalytic 1,3-dipolar cycloaddition Chem. Commun. 49 2013 3458 3460
-
(2013)
Chem. Commun.
, vol.49
, pp. 3458-3460
-
-
Wang, L.1
Shi, X.M.2
Dong, W.P.3
Zhu, L.P.4
Wang, R.5
-
28
-
-
84857977999
-
Asymmetric synthesis of allenyl oxindoles and spirooxindoles by a catalytic enantioselective Saucy-Marbet Claisen rearrangement
-
T. Cao, J. Deitch, E.C. Linton, and M.C. Kozlowski Asymmetric synthesis of allenyl oxindoles and spirooxindoles by a catalytic enantioselective Saucy-Marbet Claisen rearrangement Angew. Chem. Int. Ed. 51 2012 2448 2451
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 2448-2451
-
-
Cao, T.1
Deitch, J.2
Linton, E.C.3
Kozlowski, M.C.4
-
29
-
-
79951831704
-
One-pot synthesis of spirooxindole derivatives catalyzed by lipase in the presence of water
-
S.-J. Chai, Y.-F. Lai, J.-C. Xu, H. Zheng, Q. Zhu, and P.-F. Zhang One-pot synthesis of spirooxindole derivatives catalyzed by lipase in the presence of water Adv. Synth. Catal. 353 2011 371 375
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 371-375
-
-
Chai, S.-J.1
Lai, Y.-F.2
Xu, J.-C.3
Zheng, H.4
Zhu, Q.5
Zhang, P.-F.6
-
30
-
-
84859848338
-
Synthesis and biological evaluation of novel steroidal[17,16-d][1,2,4] triazolo[1,5-A]pyrimidines
-
L.H. Huang, Y.F. Zheng, Y.Z. Lu, C.J. Song, Y.G. Wang, B. Yu, and H.M. Liu Synthesis and biological evaluation of novel steroidal[17,16-d][1,2,4] triazolo[1,5-a]pyrimidines Steroids 77 2012 710 715
-
(2012)
Steroids
, vol.77
, pp. 710-715
-
-
Huang, L.H.1
Zheng, Y.F.2
Lu, Y.Z.3
Song, C.J.4
Wang, Y.G.5
Yu, B.6
Liu, H.M.7
-
31
-
-
84884503727
-
Design and synthesis of novel D-ring fused steroidal heterocycles
-
B.L. Zhang, E. Zhang, L.P. Pang, L.X. Song, Y.F. Li, B. Yu, and H.M. Liu Design and synthesis of novel D-ring fused steroidal heterocycles Steroids 78 2013 1200 1208
-
(2013)
Steroids
, vol.78
, pp. 1200-1208
-
-
Zhang, B.L.1
Zhang, E.2
Pang, L.P.3
Song, L.X.4
Li, Y.F.5
Yu, B.6
Liu, H.M.7
-
32
-
-
84878407754
-
An expedient approach for the synthesis of naphthyl dispiro pyrrolidine/pyrrolizidine through 1,3-dipolar cycloaddition reaction
-
P. Saravanan, S. Pushparaj, and R. Raghunathan An expedient approach for the synthesis of naphthyl dispiro pyrrolidine/pyrrolizidine through 1,3-dipolar cycloaddition reaction Tetrahedron Lett. 54 2013 3449 3452
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 3449-3452
-
-
Saravanan, P.1
Pushparaj, S.2
Raghunathan, R.3
-
33
-
-
84876125934
-
A one-pot, three-component regiospecific synthesis of dispiropyrrolidines containing a thiophenone ring via 1,3-dipolar cycloaddition reactions of azomethine ylides
-
F.M. Moghaddam, M.R. Khodabakhshi, Z. Ghahremannejad, B.K. Foroushani, and S.W. Ng A one-pot, three-component regiospecific synthesis of dispiropyrrolidines containing a thiophenone ring via 1,3-dipolar cycloaddition reactions of azomethine ylides Tetrahedron Lett. 54 2013 2520 2524
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 2520-2524
-
-
Moghaddam, F.M.1
Khodabakhshi, M.R.2
Ghahremannejad, Z.3
Foroushani, B.K.4
Ng, S.W.5
-
34
-
-
84865699791
-
Multi-component, 1,3-dipolar cycloaddition reactions for the chemo-, regio- and stereoselective synthesis of novel hybrid spiroheterocycles in ionic liquid
-
S. Michael Rajesh, B.D. Bala, and S. Perumal Multi-component, 1,3-dipolar cycloaddition reactions for the chemo-, regio- and stereoselective synthesis of novel hybrid spiroheterocycles in ionic liquid Tetrahedron Lett. 53 2012 5367 5371
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 5367-5371
-
-
Michael Rajesh, S.1
Bala, B.D.2
Perumal, S.3
-
35
-
-
84879006100
-
A strategic approach to the synthesis of novel class of dispiroheterocyclic derivatives through 1,3 dipolar cycloaddition of azomethine ylide with (E)-3-arylidene-2,3-dihydro-8-nitro-4-quinolone
-
K. Chandraprakash, M. Sankaran, C. Uvarani, R. Shankar, A. Ata, F. Dallemer, and P.S. Mohan A strategic approach to the synthesis of novel class of dispiroheterocyclic derivatives through 1,3 dipolar cycloaddition of azomethine ylide with (E)-3-arylidene-2,3-dihydro-8-nitro-4-quinolone Tetrahedron Lett. 54 2013 3896 3901
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 3896-3901
-
-
Chandraprakash, K.1
Sankaran, M.2
Uvarani, C.3
Shankar, R.4
Ata, A.5
Dallemer, F.6
Mohan, P.S.7
-
36
-
-
84880044906
-
Three-component synthesis of indanone-fused spirooxindole derivatives
-
X.-B. Chen, X.-M. Liu, R. Huang, S.-J. Yan, and J. Lin Three-component synthesis of indanone-fused spirooxindole derivatives Eur. J. Org. Chem. 2013 2013 4607 4613
-
(2013)
Eur. J. Org. Chem.
, vol.2013
, pp. 4607-4613
-
-
Chen, X.-B.1
Liu, X.-M.2
Huang, R.3
Yan, S.-J.4
Lin, J.5
-
37
-
-
42249114014
-
Review of cytotoxic cephalostatins and ritterazines: Isolation and synthesis
-
DOI 10.1021/np070536z
-
B.R. Moser Review of cytotoxic Cephalostatins and Ritterazines: isolation and synthesis J. Nat. Prod. 71 2008 487 491 (Pubitemid 351549381)
-
(2008)
Journal of Natural Products
, vol.71
, Issue.3
, pp. 487-491
-
-
Moser, B.R.1
-
38
-
-
84871541859
-
Synthesis of 14′,15′-dehydro-ritterazine y via reductive and oxidative functionalizations of hecogenin acetate
-
Y. Kou, Y. Cheun, M.C. Koag, and S. Lee Synthesis of 14′,15′- dehydro-ritterazine Y via reductive and oxidative functionalizations of hecogenin acetate Steroids 78 2013 304 311
-
(2013)
Steroids
, vol.78
, pp. 304-311
-
-
Kou, Y.1
Cheun, Y.2
Koag, M.C.3
Lee, S.4
-
39
-
-
84873049158
-
Preparation, preliminary screening of new types of steroid conjugates and their activities on steroid receptors
-
M. Jurasek, P. Dzubak, D. Sedlak, H. Dvorakova, M. Hajduch, P. Bartunek, and P. Drasar Preparation, preliminary screening of new types of steroid conjugates and their activities on steroid receptors Steroids 78 2013 356 361
-
(2013)
Steroids
, vol.78
, pp. 356-361
-
-
Jurasek, M.1
Dzubak, P.2
Sedlak, D.3
Dvorakova, H.4
Hajduch, M.5
Bartunek, P.6
Drasar, P.7
-
40
-
-
84867577877
-
A new approach to steroid dimers and macrocycles by the reaction of 3-chlorocarbonyl derivatives of bile acids with O,O-, N,N-, and S,S-dinucleophiles
-
Z. Paryzek, R. Joachimiak, M. Piasecka, and T. Pospieszny A new approach to steroid dimers and macrocycles by the reaction of 3-chlorocarbonyl derivatives of bile acids with O,O-, N,N-, and S,S-dinucleophiles Tetrahedron Lett. 53 2012 6212 6215
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 6212-6215
-
-
Paryzek, Z.1
Joachimiak, R.2
Piasecka, M.3
Pospieszny, T.4
-
41
-
-
84874008463
-
Synthesis of novel 16-spiro steroids: Spiro-7′-(aryl)tetrahydro-1H- pyrrolo[1,2-c][1,3]thiazolo-trans-androsterone hybrid heterocycles
-
S. Kanchithalaivan, R.R. Kumar, and S. Perumal Synthesis of novel 16-spiro steroids: spiro-7′-(aryl)tetrahydro-1H-pyrrolo[1,2-c][1,3] thiazolo-trans-androsterone hybrid heterocycles Steroids 78 2013 409 417
-
(2013)
Steroids
, vol.78
, pp. 409-417
-
-
Kanchithalaivan, S.1
Kumar, R.R.2
Perumal, S.3
|