-
2
-
-
0017057505
-
Ledakin-Anticancerous Medicine 1-Nitro-9-(3-dimethylaminopropylamino)acridine dihydrochloride monohydrate
-
(b) Ledochowski, A. Ledakin-Anticancerous Medicine 1-Nitro-9-(3-dimethylaminopropylamino)acridine dihydrochloride monohydrate. Mater. Med. Polon. 1976, 8, 237-251.
-
(1976)
Mater. Med. Polon.
, vol.8
, pp. 237-251
-
-
Ledochowski, A.1
-
3
-
-
0042684881
-
-
Hahn, F. E., Ed.; Springer Verlag: Berlin
-
Gniazdowski, M.; Filipsky, J.; Chorazy, M. In Antibiotics; Hahn, F. E., Ed.; Springer Verlag: Berlin, 1979; Vol. 2, pp 275-297.
-
(1979)
Antibiotics
, vol.2
, pp. 275-297
-
-
Gniazdowski, M.1
Filipsky, J.2
Chorazy, M.3
-
4
-
-
0001745393
-
-
Neidle, S., Waring, M. J., Eds.; MacMillan Publishing Co.: London
-
Denny, W. A.; Baguley, B. C.; Cain, B. F.; Waring, M. J. In Molecular Aspects of Anticancer Drug Action; Neidle, S., Waring, M. J., Eds.; MacMillan Publishing Co.: London, 1983; pp 1-34.
-
(1983)
Molecular Aspects of Anticancer Drug Action
, pp. 1-34
-
-
Denny, W.A.1
Baguley, B.C.2
Cain, B.F.3
Waring, M.J.4
-
5
-
-
0002658219
-
-
Wilman, D. E. V., Ed.; Blackie: Glasgow
-
(e) Denny, W. A. In The Chemistry of Antitumor Agents; Wilman, D. E. V., Ed.; Blackie: Glasgow, 1990; pp 1-29.
-
(1990)
The Chemistry of Antitumor Agents
, pp. 1-29
-
-
Denny, W.A.1
-
6
-
-
0017195039
-
Potential Antitumor Agents. 17. 9-Anilino-10-methylacridinium Salts
-
Cain, B. F.; Atwell, G. J.; Denny, W. A. Potential Antitumor Agents. 17. 9-Anilino-10-methylacridinium Salts. J. Med. Chem. 1976, 19, 772-777.
-
(1976)
J. Med. Chem.
, vol.19
, pp. 772-777
-
-
Cain, B.F.1
Atwell, G.J.2
Denny, W.A.3
-
7
-
-
0017744584
-
Development of Antibacterial Agents of the Nalidixic Acid Type
-
(a) Albrecht, R. Development of Antibacterial Agents of the Nalidixic Acid Type. Prog. Drug Res. 1977, 21, 9-104.
-
(1977)
Prog. Drug Res.
, vol.21
, pp. 9-104
-
-
Albrecht, R.1
-
8
-
-
0003822982
-
-
Lukacz, G., Ohno, M., Eds.; Springer Verlag: Berlin
-
(b) Bouzard, D. In Recent Progress in the Chemical Synthesis of Antibiotics: Recent Advances in the Chemistry of Quinolones: Lukacz, G., Ohno, M., Eds.; Springer Verlag: Berlin, 1990; p 249.
-
(1990)
Recent Progress in the Chemical Synthesis of Antibiotics: Recent Advances in the Chemistry of Quinolones
, pp. 249
-
-
Bouzard, D.1
-
11
-
-
0027715756
-
A Novel Nucleophilic Substitution with Quinoline Derivatives. Synthesis of Quinolones and Pyrazolo-[4,3-c]quinoline Derivatives
-
and references cited herein
-
Mekheimer, R.; Ahmed, E. Kh.; Khattab, A. F. A Novel Nucleophilic Substitution with Quinoline Derivatives. Synthesis of Quinolones and Pyrazolo-[4,3-c]quinoline Derivatives. Bull. Chem. Soc. Jpn. 1993, 66, 2936-2940 and references cited herein.
-
(1993)
Bull. Chem. Soc. Jpn.
, vol.66
, pp. 2936-2940
-
-
Mekheimer, R.1
Ahmed, E.Kh.2
Khattab, A.F.3
-
12
-
-
14444278056
-
-
Ger. Offen. 2,407,744, 1974
-
(a) Ridgway, M. H.; Waters, M. D.; Peel, E. M.; Ellis, P. G. Tetrazolyloxodihydroquinoline Carboxamides. Ger. Offen. 2,407,744, 1974.
-
Tetrazolyloxodihydroquinoline Carboxamides
-
-
Ridgway, M.H.1
Waters, M.D.2
Peel, E.M.3
Ellis, P.G.4
-
13
-
-
0016767945
-
4-Hydroxy-3-nitro-2-quinolones and Related Compounds as Inhibitors of Allergic Reactions
-
(b) Buckle, D. R.; Cantello, B. C. C.; Smith, H. H.; Spicer, B. A. 4-Hydroxy-3-nitro-2-quinolones and Related Compounds as Inhibitors of Allergic Reactions. J. Med. Chem. 1975, 18, 726-732.
-
(1975)
J. Med. Chem.
, vol.18
, pp. 726-732
-
-
Buckle, D.R.1
Cantello, B.C.C.2
Smith, H.H.3
Spicer, B.A.4
-
14
-
-
14444272992
-
-
U.S. Patent 4,748,246, 1988
-
Stotnichi, S. J.; Gilman, C. S.; Steinbaugh, A. B.; Musser, H. J. Preparation of Pyrazolo[4,3-c]quinolines as Antiinflammatories. U.S. Patent 4,748,246, 1988.
-
Preparation of Pyrazolo[4,3-c]quinolines As Antiinflammatories
-
-
Stotnichi, S.J.1
Gilman, C.S.2
Steinbaugh, A.B.3
Musser, H.J.4
-
15
-
-
14444283864
-
-
Ger. Offen. DE 3,716,512, 1988
-
Schubert, J.; Wild, J.; Roeser, K.; Sauter, H.; Pommer, E. H. Preparation of 2-Anilinoquinolines as Agrochemical Fungicides. Ger. Offen. DE 3,716,512, 1988.
-
Preparation of 2-Anilinoquinolines As Agrochemical Fungicides
-
-
Schubert, J.1
Wild, J.2
Roeser, K.3
Sauter, H.4
Pommer, E.H.5
-
16
-
-
14444281998
-
-
U.S. Patent 4,920,128, 1990
-
Bell, R. M.; Ackerman, H. Preparation of Pyrazolo[3,4-b]quinolines as Antiviral Agents. U.S. Patent 4,920,128, 1990.
-
Preparation of Pyrazolo[3,4-b]quinolines As Antiviral Agents
-
-
Bell, R.M.1
Ackerman, H.2
-
17
-
-
0018387471
-
Synthesis of Antimicrobial Agents. Y. Synthesis and Antimicrobial Activities of Thiazoloquinoline Derivatives
-
(a) Suzuki, N.; Tamaka, Y.; Domori, R. Synthesis of Antimicrobial Agents. Y. Synthesis and Antimicrobial Activities of Thiazoloquinoline Derivatives. Chem. Pharm. Bull. 1979, 27, 1-11.
-
(1979)
Chem. Pharm. Bull.
, vol.27
, pp. 1-11
-
-
Suzuki, N.1
Tamaka, Y.2
Domori, R.3
-
18
-
-
0017238674
-
Synthetic Chemotherapeutic Agents. Y. Synthesis of 2-Substituted Thiazolo[5,4-f]quinoline Derivatives
-
(b) Domori, R.; Kadoya, S.; Takamura, Y.; Suzuki, N. Synthetic Chemotherapeutic Agents. Y. Synthesis of 2-Substituted Thiazolo[5,4-f]quinoline Derivatives. Chem. Pharm. Bull. 1976, 24, 130-135.
-
(1976)
Chem. Pharm. Bull.
, vol.24
, pp. 130-135
-
-
Domori, R.1
Kadoya, S.2
Takamura, Y.3
Suzuki, N.4
-
19
-
-
14444284339
-
-
Japan Kokai 77,125,196, 1978
-
Suzuki, N.; Nagata, Y.; Tanaka, Y.; Domori, R. Thiazoloquinolinecarboxylic Acids. Japan Kokai 77,125,196, 1978.
-
Thiazoloquinolinecarboxylic Acids
-
-
Suzuki, N.1
Nagata, Y.2
Tanaka, Y.3
Domori, R.4
-
20
-
-
14444284339
-
-
Japan Kokai 77,83,596, 1978
-
Suzuki, N.; Nagata, Y.; Tanaka, Y.; Domori, R. Thiazoloquinolinecarboxylic Acids. Japan Kokai 77,83,596, 1978.
-
Thiazoloquinolinecarboxylic Acids
-
-
Suzuki, N.1
Nagata, Y.2
Tanaka, Y.3
Domori, R.4
-
21
-
-
0018393843
-
Synthetic Chemotherapeutic Agents. V. Antibacterial Activities of Thiazolo[5,4-f]-quinolinecarboxylic Acid Derivatives
-
(e) Kadoya, S.; Nagasaki, S. Synthetic Chemotherapeutic Agents. V. Antibacterial Activities of Thiazolo[5,4-f]-quinolinecarboxylic Acid Derivatives. Yakugaku Zasshi 1979, 99, 483-920.
-
(1979)
Yakugaku Zasshi
, vol.99
, pp. 483-920
-
-
Kadoya, S.1
Nagasaki, S.2
-
22
-
-
14444267324
-
Thiazoloquinolines. II. Thiazolo[5,4-b]quinoline Substituted in the thiazole Ring
-
(a) Tanasescu, Y.; Denes, Y.; Rusus, G. Thiazoloquinolines. II. Thiazolo[5,4-b]quinoline Substituted in the thiazole Ring. Chem. Ber. 1957, 90, 1295-1299.
-
(1957)
Chem. Ber.
, vol.90
, pp. 1295-1299
-
-
Tanasescu, Y.1
Denes, Y.2
Rusus, G.3
-
23
-
-
14444271800
-
Thiazoloquinolines. IV. the Chlorination of the 2-Mercapto Derivatives of Thiazolo[4,5-b]- And [5,4-b]quinoline
-
(b) Tanasescu, Y.; Denes, Y.; Rusus, G. Thiazoloquinolines. IV. The Chlorination of the 2-Mercapto Derivatives of Thiazolo[4,5-b]- and [5,4-b]quinoline. Chem. Ber. 1959, 92, 869-871.
-
(1959)
Chem. Ber.
, vol.92
, pp. 869-871
-
-
Tanasescu, Y.1
Denes, Y.2
Rusus, G.3
-
24
-
-
14444272991
-
Thiazoloquinolines. V. Some Alkylation Reactions of 2-Hydroxythiazolo[4,5-b]- And [5,4-b]quinolines
-
Tanasescu, Y.; Denes, Y.; Makkay, K. Thiazoloquinolines. V. Some Alkylation Reactions of 2-Hydroxythiazolo[4,5-b]- and [5,4-b]quinolines. Chem. Ber. 1959, 92, 2779-2783.
-
(1959)
Chem. Ber.
, vol.92
, pp. 2779-2783
-
-
Tanasescu, Y.1
Denes, Y.2
Makkay, K.3
-
25
-
-
0003605774
-
Antispasmodic Compounds
-
Sabata, B. K.; Tripathy, P. B.; Rout, M. K. Antispasmodic Compounds. J. Proc. Inst. Chem. 1960, 32, 147-150.
-
(1960)
J. Proc. Inst. Chem.
, vol.32
, pp. 147-150
-
-
Sabata, B.K.1
Tripathy, P.B.2
Rout, M.K.3
-
26
-
-
14444269673
-
Benzothiazolylalkanoic Acids and Their derivatives. VI. Condensation of 2-amino-1-thionaphtol and 3-amino-2-mercaptoquinoline with the Anhydrides of Dibasic Carboxylic Acids
-
Kiprianova, L. A.; Yarovi, D. K.; Schetsinskaya, E.; Babiechev, F. S. Benzothiazolylalkanoic Acids and Their derivatives. VI. Condensation of 2-amino-1-thionaphtol and 3-amino-2-mercaptoquinoline with the Anhydrides of Dibasic Carboxylic Acids. Ukr. Khim. Zh. 1964, 30, 859-862.
-
(1964)
Ukr. Khim. Zh.
, vol.30
, pp. 859-862
-
-
Kiprianova, L.A.1
Yarovi, D.K.2
Schetsinskaya, E.3
Babiechev, F.S.4
-
27
-
-
14444279657
-
Potential Antispasmodics. Quinolinothiazoles
-
Das, B.; Rout, M. K. Potential Antispasmodics. Quinolinothiazoles. J. Sci. Ind. Res. 1957, 16C, 125-126.
-
(1957)
J. Sci. Ind. Res.
, vol.16 C
, pp. 125-126
-
-
Das, B.1
Rout, M.K.2
-
28
-
-
14444273226
-
Cyanine Dyes Derived from Thiazoloquinolines
-
Modica, G. di; Barni, E. Cyanine Dyes Derived from Thiazoloquinolines. Gazz. Chim. Ital. 1963, 93, 679-686.
-
(1963)
Gazz. Chim. Ital.
, vol.93
, pp. 679-686
-
-
Di Modica, G.1
Barni, E.2
-
29
-
-
14344285363
-
-
Ger. Offen. DE 3,533,331, 1987
-
Moersdorf, P.; Schickaneder, H.; Engler, H.; Ahrens, K. H. Preparation of Hydrazinothiazolopyridines as Antiinflammatories. Ger. Offen. DE 3,533,331, 1987.
-
Preparation of Hydrazinothiazolopyridines As Antiinflammatories
-
-
Moersdorf, P.1
Schickaneder, H.2
Engler, H.3
Ahrens, K.H.4
-
30
-
-
0027536887
-
Chloroisotiocyanatoquinolines as Fluoregenic Derivatizing Agents for Primary and Secondary Amines
-
Bernstein, S. C.; Abrams, S. K.; Leckrone, K. J.; Paul, L. A. Chloroisotiocyanatoquinolines as Fluoregenic Derivatizing Agents for Primary and Secondary Amines. J. Pharm. Biomed. Anal. 1993, 11, 61-69.
-
(1993)
J. Pharm. Biomed. Anal.
, vol.11
, pp. 61-69
-
-
Bernstein, S.C.1
Abrams, S.K.2
Leckrone, K.J.3
Paul, L.A.4
-
31
-
-
1542391675
-
A One-pot Preparation of dimethyl N-alkyliminodithiocarbonates
-
Ethyl N-[bis(methylthio)methylene]glycinate is easily obtained in a single step from ethyl glycinate, carbon disulfide, and methyl idodide; see: Alvarez-Ibarra, C.; Quiroga, M. L.; Toledano, E. A One-pot Preparation of dimethyl N-alkyliminodithiocarbonates. Org. Prep. Proc. Int. 1991, 23, 611-616.
-
(1991)
Org. Prep. Proc. Int.
, vol.23
, pp. 611-616
-
-
Alvarez-Ibarra, C.1
Quiroga, M.L.2
Toledano, E.3
-
32
-
-
84982362635
-
Chain-Extended and α-Branched α-Amino Acids by Alkylation of Metalated α-[Bis(methylthio)-methylene]amino Acid Esters
-
Representative articles on the first usages of N-[bis(methylthio)-methylene]glycine ester enolates for glycine anion reagents are as follows: (a) Hoppe, D. Chain-Extended and α-Branched α-Amino Acids by Alkylation of Metalated α-[Bis(methylthio)-methylene]amino Acid Esters. Angew. Chem., Int. Ed. Engl. 1975, 14, 426-427. (b) Hoppe, D.; Beckmann, L. Metalated Nitrogen Derivatives of Carbonic Acid in Organic Synthesis. XIII. Selective Mono- and Dialkylation of N-[Bis(methylthio)-methylene]glycine Ester for Synthesis of Higher and α-Branched α-Amino Acids. Liebigs Ann. Chem. 1979, 2066-2075.
-
(1975)
Angew. Chem., Int. Ed. Engl.
, vol.14
, pp. 426-427
-
-
Hoppe, D.1
-
33
-
-
84914333688
-
Metalated Nitrogen Derivatives of Carbonic Acid in Organic Synthesis. XIII. Selective Mono- and Dialkylation of N-[Bis(methylthio)-methylene]glycine Ester for Synthesis of Higher and α-Branched α-Amino Acids
-
Representative articles on the first usages of N-[bis(methylthio)-methylene]glycine ester enolates for glycine anion reagents are as follows: (a) Hoppe, D. Chain-Extended and α-Branched α-Amino Acids by Alkylation of Metalated α-[Bis(methylthio)-methylene]amino Acid Esters. Angew. Chem., Int. Ed. Engl. 1975, 14, 426-427. (b) Hoppe, D.; Beckmann, L. Metalated Nitrogen Derivatives of Carbonic Acid in Organic Synthesis. XIII. Selective Mono- and Dialkylation of N-[Bis(methylthio)-methylene]glycine Ester for Synthesis of Higher and α-Branched α-Amino Acids. Liebigs Ann. Chem. 1979, 2066-2075.
-
(1979)
Liebigs Ann. Chem.
, pp. 2066-2075
-
-
Hoppe, D.1
Beckmann, L.2
-
34
-
-
0011430504
-
An Efficient Synthesis of 5-Aryl- (or alkyl)amino-4-ethoxycarbonyl-2-methylthio-1,3-thiazoles from Dimethyl N-(Ethoxycarbonylmethyl)-iminodithiocarbonate and Isothiocyanates
-
Alvarez-Ibarra, C.; Gil, M.; Ortiz, P.; Quiroga, M. L. An Efficient Synthesis of 5-Aryl-(or alkyl)amino-4-ethoxycarbonyl-2-methylthio-1,3-thiazoles from Dimethyl N-(Ethoxycarbonylmethyl)-iminodithiocarbonate and Isothiocyanates. Heterocycles 1988, 27, 2177-2183.
-
(1988)
Heterocycles
, vol.27
, pp. 2177-2183
-
-
Alvarez-Ibarra, C.1
Gil, M.2
Ortiz, P.3
Quiroga, M.L.4
-
35
-
-
37049101570
-
Nitrogen Bridgedhead Compounds. Part 4. 1-3-N-C-Acyl Migration
-
Hermecz, Y.; Mèszáros, Z.; Vasvari-Debreczy, L.; Horváth, G.; Ponger-Csákvar, M. Nitrogen Bridgedhead Compounds. Part 4. 1-3-N-C-Acyl Migration. J. Chem. Soc., Perkin Trans. 1 1977, 789-795.
-
(1977)
J. Chem. Soc., Perkin Trans. 1
, pp. 789-795
-
-
Hermecz, Y.1
Mèszáros, Z.2
Vasvari-Debreczy, L.3
Horváth, G.4
Ponger-Csákvar, M.5
-
36
-
-
0026008534
-
Thiazolo[5,4-b]acridines and thiazolo[4,5-b]acridines: Probable Pharmacophores of Antiviral and Anti-tumor Marine Alkaloids
-
Taporewala, Y. B. Thiazolo[5,4-b]acridines and thiazolo[4,5-b]acridines: Probable Pharmacophores of Antiviral and Anti-tumor Marine Alkaloids. Tetrahedron Lett. 1991, 32, 39-42.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 39-42
-
-
Taporewala, Y.B.1
-
37
-
-
13044271366
-
Synthesis of p-Nitrophenyl Ester of Acridine-2-acetic Acid
-
Kaufman, J. M.; Taporewala, Y. B. Synthesis of p-Nitrophenyl Ester of Acridine-2-acetic Acid. J. Heterocycl. Chem. 1982, 19, 1557-1559.
-
(1982)
J. Heterocycl. Chem.
, vol.19
, pp. 1557-1559
-
-
Kaufman, J.M.1
Taporewala, Y.B.2
-
38
-
-
0024997709
-
Synthesis of Des-N-methylacronycine and Acronycine
-
Laughead, D. G. Synthesis of Des-N-methylacronycine and Acronycine. J. Org. Chem. 1990, 55, 2245-2246.
-
(1990)
J. Org. Chem.
, vol.55
, pp. 2245-2246
-
-
Laughead, D.G.1
-
39
-
-
0021681136
-
Thiazolopyridine Analogs of Nalidixic Acid. 2. Thiazolo[4,5-b]pyridines
-
Leysen, D. C.; Haemers, A.; Bollaert, W. Thiazolopyridine Analogs of Nalidixic Acid. 2. Thiazolo[4,5-b]pyridines. J. Heterocycl. Chem. 1984, 21, 1361-1366.
-
(1984)
J. Heterocycl. Chem.
, vol.21
, pp. 1361-1366
-
-
Leysen, D.C.1
Haemers, A.2
Bollaert, W.3
-
40
-
-
0010995106
-
Synthesis of sulfoxides by oxidation of thioethers
-
(a) Madesclaire, M. Synthesis of sulfoxides by oxidation of thioethers. Tetrahedron 1986, 42, 5459-5495.
-
(1986)
Tetrahedron
, vol.42
, pp. 5459-5495
-
-
Madesclaire, M.1
-
41
-
-
84980197939
-
Polycyclic Thiazoles. I. Anionic Nucleophilic Substitution on 2-methylsulfonyl derivatives of thiazolo[5,4-b]pyridine and Benzothiazoles
-
(b) Bourdais, J.; Abenhain, D.; Saborault, B.; Lorre, A. Polycyclic Thiazoles. I. Anionic Nucleophilic Substitution on 2-methylsulfonyl derivatives of thiazolo[5,4-b]pyridine and Benzothiazoles. J. Heterocycl. Chem. 1976, 13, 491-496.
-
(1976)
J. Heterocycl. Chem.
, vol.13
, pp. 491-496
-
-
Bourdais, J.1
Abenhain, D.2
Saborault, B.3
Lorre, A.4
-
42
-
-
0018199203
-
Potential Antitumor Agents. 28. Deoxyribonucleic Acid Polyintercalating Agents
-
Cain, B. F.; Baguley, B. C.; Denny, W. A. Potential Antitumor Agents. 28. Deoxyribonucleic Acid Polyintercalating Agents. J. Med. Chem. 1978, 21, 658-668.
-
(1978)
J. Med. Chem.
, vol.21
, pp. 658-668
-
-
Cain, B.F.1
Baguley, B.C.2
Denny, W.A.3
-
43
-
-
37049140247
-
Useful Reactions of Nucleophiles with Some Methylsulphonyl Derivatives of Nitrogen Heterocycles
-
(a) Barlin, G. B.; Brown, W. V. Useful Reactions of Nucleophiles with Some Methylsulphonyl Derivatives of Nitrogen Heterocycles. J. Chem. Soc. C 1967, 2473-2476.
-
(1967)
J. Chem. Soc. C
, pp. 2473-2476
-
-
Barlin, G.B.1
Brown, W.V.2
-
44
-
-
0037929835
-
Simple Pyrimidines. Part X. the Formation and Reactivity of 2-, 4-, and 5-Pyrimidinyl Sulphones and Sulphoxides
-
(b) Brown, D. J.; Ford, P. W. Simple Pyrimidines. Part X. The Formation and Reactivity of 2-, 4-, and 5-Pyrimidinyl Sulphones and Sulphoxides. J. Chem. Soc. C 1967, 568-572.
-
(1967)
J. Chem. Soc. C
, pp. 568-572
-
-
Brown, D.J.1
Ford, P.W.2
-
45
-
-
4444225697
-
A New Synthetic Approximation to Thiazoles with a Versatile Persubstitution and/or Perfunctionalization
-
Alvarez-Ibarra, C.; Asperilla, R.; Dios-Corredor, C. de; Martinez-Santos, E.; Quiroga, M. L. A New Synthetic Approximation to Thiazoles with a Versatile Persubstitution and/or Perfunctionalization. Heterocycles 1991, 32, 2127-2137.
-
(1991)
Heterocycles
, vol.32
, pp. 2127-2137
-
-
Alvarez-Ibarra, C.1
Asperilla, R.2
De Dios-Corredor, C.3
Martinez-Santos, E.4
Quiroga, M.L.5
-
46
-
-
14444273877
-
Synthesis of Substituted 4-Aminoquinolines
-
(a) Price, C. C.; Boekelheide, V. A Synthesis of Substituted 4-Aminoquinolines. J. Am. Chem. Soc. 1946, 68, 1246-1250.
-
(1946)
J. Am. Chem. Soc.
, vol.68
, pp. 1246-1250
-
-
Price, C.C.1
Boekelheide, V.A.2
-
47
-
-
14444270357
-
Attempts to Find New Antimalarials. Part XV. the Synthesis of Acridine Compounds Related to Atebrin
-
(b) Goodall, R.; Kermack, W. O. Attempts to Find New Antimalarials. Part XV. The Synthesis of Acridine Compounds Related to Atebrin. J. Chem. Soc. 1936, 1546-1550.
-
(1936)
J. Chem. Soc.
, pp. 1546-1550
-
-
Goodall, R.1
Kermack, W.O.2
-
48
-
-
0001256192
-
Synthesis of (±)-Cularicine
-
Noguchi, I.; MacLean, D. B. Synthesis of (±)-Cularicine. Can. J. Chem. 1975, 53, 125-130.
-
(1975)
Can. J. Chem.
, vol.53
, pp. 125-130
-
-
Noguchi, I.1
MacLean, D.B.2
-
49
-
-
14444269465
-
-
John Wiley: New York, and references cited herein
-
Olah, G. A. Friedel-Crafts Chemistry; John Wiley: New York, 1973; Vol. 1, pp 216-217, 272-273, 312-316 and references cited herein.
-
(1973)
Friedel-Crafts Chemistry
, vol.1
, pp. 216-217
-
-
Olah, G.A.1
-
51
-
-
0030565486
-
a Values for Polycationic Species Derived from 9-Hydroxy- and 9-Aminothiazolo[5,4-b]quinolines. A Problem Related to the Tautomerism of these Systems
-
a Values for Polycationic Species Derived from 9-Hydroxy- and 9-Aminothiazolo[5,4-b]quinolines. A Problem Related to the Tautomerism of these Systems. Tetrahedron 1996, 52, 11929-11946.
-
(1996)
Tetrahedron
, vol.52
, pp. 11929-11946
-
-
Alvarez-Ibarra, C.1
Fernández-Granda, R.2
Quiroga, M.L.3
Pingarrón, J.M.4
Pedrero, M.5
-
52
-
-
0003688714
-
-
Springer Verlag: Berlin
-
Pretsch, E.; Clerc, T.; Seibl, J.; Simon, W. Tables of Spectral Data for Structural Determination of Organic Compounds, 2nd ed.; Springer Verlag: Berlin, 1989.
-
(1989)
Tables of Spectral Data for Structural Determination of Organic Compounds, 2nd Ed.
-
-
Pretsch, E.1
Clerc, T.2
Seibl, J.3
Simon, W.4
-
53
-
-
14444279656
-
-
note
-
For induced chemical shifts for a methyl group and a fluorine atom in a benzene ring, see ref 32.
-
-
-
-
54
-
-
14444284571
-
-
note
-
The correlation coefficient for the linear regression between observed and calculated chemical shifts was 0.959 (30 data points).
-
-
-
-
55
-
-
14444278275
-
-
note
-
Hydrogens H-7 and H-6 for compounds 8 and 10 appeared as a doublet of doublet of doublets (ddd), hydrogens H-5 (compound 10) and H-8 (compounds 8 and 10) appeared as a doublet of doublets (dd), hydrogens H-6 and H-5 for compound 9 appeared as a doublet, and the signal of H-8 for compound 9 was a broad singlet.
-
-
-
-
56
-
-
14444287513
-
-
note
-
37
-
-
-
-
58
-
-
14444275057
-
-
See ref 32, p 74
-
See ref 32, p 74.
-
-
-
-
59
-
-
14444281541
-
-
note
-
The correlation coefficient for the linear regression between observed and calculated chemical shifts was 0.989 (60 data points).
-
-
-
-
61
-
-
14444288536
-
Experimental and Theoretical Studies of the Carbon-13 Chemical Shifts in a Series of Isothiazoles
-
(b) Faure, R.; Llinas, J. R.; Vicent, E. J.; Rajzmann, M. Experimental and Theoretical Studies of the Carbon-13 Chemical Shifts in a Series of Isothiazoles. Can. J. Chem. 1975, 53, 1677-1681.
-
(1975)
Can. J. Chem.
, vol.53
, pp. 1677-1681
-
-
Faure, R.1
Llinas, J.R.2
Vicent, E.J.3
Rajzmann, M.4
-
62
-
-
0000844099
-
Studies in the Field of natural Product Chemistry. Part 63. Carbon-13 NMR Spectra of Acridone Alkaloids
-
Bergental, D.; Mester, Y.; Rosza, Z. S.; Reisch, J. Studies in the Field of natural Product Chemistry. Part 63. Carbon-13 NMR Spectra of Acridone Alkaloids. Phytochemistry 1979, 18, 161-163.
-
(1979)
Phytochemistry
, vol.18
, pp. 161-163
-
-
Bergental, D.1
Mester, Y.2
Rosza, Z.S.3
Reisch, J.4
-
63
-
-
0000718198
-
Carbon-13 Nuclear Magnetic Resonance of Pyridine N-Oxide
-
Anet, F. L.; Yavari, I. Carbon-13 Nuclear Magnetic Resonance of Pyridine N-Oxide. J. Org. Chem. 1976, 41, 3589-3591.
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3589-3591
-
-
Anet, F.L.1
Yavari, I.2
-
64
-
-
24444468650
-
Ground States of Molecules. 38. Method Approximations and Parameters
-
(a) Dewar, M. J. S.; Thiel, W. Ground States of Molecules. 38. Method Approximations and Parameters. J. Am. Chem. Soc. 1977, 99, 4899-4907.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 4899-4907
-
-
Dewar, M.J.S.1
Thiel, W.2
-
65
-
-
33847087937
-
Ground States of Molecules. 39. MNDO Results for Molecules Containing Hydrogen, Carbon, Nitrogen, and Oxygen
-
(b) Dewar, M. J. S.; Thiel, W. Ground States of Molecules. 39. MNDO Results for Molecules Containing Hydrogen, Carbon, Nitrogen, and Oxygen. J. Am. Chem. Soc. 1977, 99, 4907-4917.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 4907-4917
-
-
Dewar, M.J.S.1
Thiel, W.2
-
66
-
-
84986435889
-
Ground States of Molecules. 56. MNDO Calculations for Molecules Containing Sulfur
-
Dewar, M. J. S.; McKee, M. L. Ground States of Molecules. 56. MNDO Calculations for Molecules Containing Sulfur. J. Comput. Chem. 1983, 4, 84-103.
-
(1983)
J. Comput. Chem.
, vol.4
, pp. 84-103
-
-
Dewar, M.J.S.1
McKee, M.L.2
-
67
-
-
0001810980
-
Reactivity of Naphthyridines toward Nitrogen Nucleophiles
-
(a) van der Plas, H. C.; Wozniak, M.; van der Haak, H. J. W. Reactivity of Naphthyridines toward Nitrogen Nucleophiles. Adv. Heterocycl. Chem. 1983, 33, 95.
-
(1983)
Adv. Heterocycl. Chem.
, vol.33
, pp. 95
-
-
Plas, H.C.1
Wozniak, M.2
Van Der Haak, H.J.W.3
-
68
-
-
4143130860
-
Recent Developments in Naphthyridine Chemistry
-
(b) Paudler, W. W.; Sheets, R. M. Recent Developments in Naphthyridine Chemistry. Adv. Heterocycl. Chem. 1983, 33, 147.
-
(1983)
Adv. Heterocycl. Chem.
, vol.33
, pp. 147
-
-
Paudler, W.W.1
Sheets, R.M.2
-
70
-
-
14444272990
-
-
note
-
50 values stand for the concentration of sample which inhibits 50% of normal cell culture growth in the exponential phase.
-
-
-
-
71
-
-
14444274826
-
-
Fig. P and P.Fit. Fig. P Software Corp., Cambridge, U.K., version 6.0a, 1991
-
Fig. P and P.Fit. Fig. P Software Corp., Cambridge, U.K., version 6.0a, 1991.
-
-
-
-
72
-
-
14444271799
-
-
note
-
50 = 7.4 μM of 18c (for P-388 cell line).
-
-
-
-
73
-
-
14444275056
-
-
note
-
50 data (μM) against lymphoid neoplasm P-388 cell line in culture have been used as comparative results.
-
-
-
-
74
-
-
0023740270
-
Dercitin, a New Biologically Active Acridine Alkaloid from a Deep Water Marine Sponge, Dercitus sp
-
(a) Gunawardana, G. P.; Kohmoto, S.; Gunasekera, S. P.; McConnell, O. J.; Koehn, F. E. Dercitin, a New Biologically Active Acridine Alkaloid from a Deep Water Marine Sponge, Dercitus sp. J. Am. Chem. Soc. 1988, 110, 4856-4858.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 4856-4858
-
-
Gunawardana, G.P.1
Kohmoto, S.2
Gunasekera, S.P.3
McConnell, O.J.4
Koehn, F.E.5
-
75
-
-
0024373982
-
New Cytotoxic Acridine Alkaloids from Two Deep Water Marine Sponges of the Family Pachas trellidae
-
(b) Gunawardana, G. P.; Kohmoto, S.; Burres, N. S. New Cytotoxic Acridine Alkaloids from Two Deep Water Marine Sponges of the Family Pachas trellidae. Tetrahedron Lett. 1989, 30, 4359-4362.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 4359-4362
-
-
Gunawardana, G.P.1
Kohmoto, S.2
Burres, N.S.3
-
76
-
-
14444285981
-
-
50 values for dercitin (26): 0.08 μM (ref 49b) and 0.14 μM (ref 49a)
-
50 values for dercitin (26): 0.08 μM (ref 49b) and 0.14 μM (ref 49a).
-
-
-
-
77
-
-
0029008124
-
3-Benzylquinolones: Novel, Potent Inhibitors of Mammalian Topoisomerase II
-
Eisenstat, M. A.; Kuo, G.-H.; Weaver, J. D., III; Wentland, M. P.; Robinson, R. G.; Klingbeil, K. M.; Danz, D. W.; Corbett, T. H.; Couglin, S. A. 3-Benzylquinolones: Novel, Potent Inhibitors of Mammalian Topoisomerase II. Bioorg. Med. Chem. Lett. 1995, 5, 1021-1026.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 1021-1026
-
-
Eisenstat, M.A.1
Kuo, G.-H.2
Weaver III, J.D.3
Wentland, M.P.4
Robinson, R.G.5
Klingbeil, K.M.6
Danz, D.W.7
Corbett, T.H.8
Couglin, S.A.9
-
78
-
-
0028796930
-
The Antitumor Activity of Novel Pyrazoloquinoline Derivatives
-
Wentland, M. P.; Aldous, S. C.; Gruett, M. D.; Perni, R. B.; Powles, R. G.; Danz, D. W.; Klingbeil, K. M.; Peverly, A. D.; Robinson, R. G.; Corbett, T. H.; Rake, J. B.; Coughlin, S. A. The Antitumor Activity of Novel Pyrazoloquinoline Derivatives. Bioorg. Med. Chem. Lett. 1995, 5, 405-410.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 405-410
-
-
Wentland, M.P.1
Aldous, S.C.2
Gruett, M.D.3
Perni, R.B.4
Powles, R.G.5
Danz, D.W.6
Klingbeil, K.M.7
Peverly, A.D.8
Robinson, R.G.9
Corbett, T.H.10
Rake, J.B.11
Coughlin, S.A.12
-
79
-
-
0003497661
-
Thiazole and Its Derivatives
-
Metzger, J. V., Ed.; Wiley: New York, Part 1
-
(a) Meyer, R. Thiazole and Its Derivatives. In The Chemistry of Heterocyclic Compounds; Metzger, J. V., Ed.; Wiley: New York, 1979; Part 1, Vol. 34, pp 519-531.
-
(1979)
The Chemistry of Heterocyclic Compounds
, vol.34
, pp. 519-531
-
-
Meyer, R.1
-
80
-
-
0013695693
-
Thiazole Carboxylic Acids
-
(b) Erlenmeyer, H.; Junod, J.; Guex, W.; Erne, M. Thiazole Carboxylic Acids. Helv. Chim. Acta 1948, 31, 1342-1349.
-
(1948)
Helv. Chim. Acta
, vol.31
, pp. 1342-1349
-
-
Erlenmeyer, H.1
Junod, J.2
Guex, W.3
Erne, M.4
-
81
-
-
0021271378
-
Antineoplastic and Antiherpetic Activity of Spermidine Cathecholamide Iron Chelators
-
Bergeron, R. J.; Cavanaugh, P. F., Jr.; Kline, S. J.; Hughes, R. G., Jr.; Elliot, G. T.; Porter, C. W. Antineoplastic and Antiherpetic Activity of Spermidine Cathecholamide Iron Chelators. Biochem. Biophys. Res. Commun. 1984, 21, 848-854.
-
(1984)
Biochem. Biophys. Res. Commun.
, vol.21
, pp. 848-854
-
-
Bergeron, R.J.1
Cavanaugh Jr., P.F.2
Kline, S.J.3
Hughes Jr., R.G.4
Elliot, G.T.5
Porter, C.W.6
|