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11. |
Synthesis of 2,2′‐bipyrimidine derivatives |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 47-49
B. A. Feit,
A. Teuerslein,
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摘要:
AbstractA new total synthesis of 2,2′ ‐bipyrimidine derivatives by the direct condensation of 2‐amidinopyrimidinebenzenesulfonate with dicarbonyl compounds is described. The following 2,2′‐bipyrimidines have been prepared: 5‐ethyl‐4,6‐dihydroxy‐2,2′‐bipyrimidine; 5‐ethyl‐4,6‐dichloro‐2,2 ‐bipyrimidine; 4,6‐dihydroxy‐2,2′ ‐bipyrimidine; 5
ISSN:0022-152X
DOI:10.1002/jhet.5570100111
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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12. |
Acyl Indoles. III. The synthesis of [1,4] diazcpino [6,5‐b ]indoles |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 51-53
E. E. Garcia,
L. E. Benjamin,
R. Ian Fryer,
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摘要:
AbstractThe synthesis of 1,3,4,6‐letrahydro‐6‐metliy]‐2H,5H‐[1,4]diazepino[6,5‐b] indole‐2,5‐diones and 5‐phenyl‐3,6‐dihydro[1,4]diazepino[6,5‐b]indole‐2(lH)one is described. Also detailed is the, preparation of
ISSN:0022-152X
DOI:10.1002/jhet.5570100112
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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13. |
Studies on the hydrolysis of cyclophosphamide II. Isolation and characterization of intermediate hydrolytic products |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 55-58
Jiban K. Chakrabarli,
Orrie M. Friedman,
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摘要:
AbstractTwo new products of hydrolysis of cyclophosphamide in water at 100°,N‐(2‐chloroethyl)‐N' ‐(3‐phosphatopropy l)ethylenediamine andN‐(2‐hydroxyethyl)‐N‐(3‐phosphatopropyl)ethylene‐diamine, have been isolated after 30 minutes, and 6 hours of reaction times, respectively. These products have been shown to be intermediates leading to the formation ofN‐(2‐hydroxyethyl)‐N'‐(3‐hydroxypropyl)ethylenediamine, the principal ultimate product of cyclophosphamide hydrolysis. The nature of these new products supports the previously postulated mechanism involving an intramolecular alkylation as the initial step in the hydrolytic process although the pathway appears to be an unlikely model for the metabolic transforma
ISSN:0022-152X
DOI:10.1002/jhet.5570100113
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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14. |
3‐Amino‐1‐[2‐(2‐ethoxyethoxy)ethoxy ] benzo[∫]quinazoline |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 59-63
Sisir K. Sengupta,
Heljo Kangur Protopapa,
Edward J. Modest,
Bhupesh C. Das,
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摘要:
AbstractThe structure of an anomalous product, isolated as a companion substance during the catalytic dehydrogenation of 1,3‐diamino‐5,6‐dihydrobenzo[ƒ] quinazoline, has been elucidated with the aid of chemical and spectral evidence, including mass spectrometric data. The mass spectrometric fragmentation pattern of the compound is in good agreement with the assigned str
ISSN:0022-152X
DOI:10.1002/jhet.5570100114
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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15. |
Synthesis of Indolo and benzimidazoquinazolines and benzodiazepines |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 65-70
Robert L. Duncan,
Grover C. Helsley,
Robert F. Boswell,
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摘要:
AbstractIndolo[1,2‐c] quinazolines, indolo[1,2‐d] [1,4]benzodiazepines, indolo [1,2‐d] [1,4]benzodi‐azepin‐6‐ones and benzimidazo[1,2‐d] [1,4]benzodiazepin‐6‐ones were synthesized. In an acid medium, the indoloquinazolines were produced from 2‐(o‐aminophenyl)indole and acyl halides. However, in the presence of sodium acetate, the acylated amine was obtained and was cyclized to the indolobenzodiazepinones using sodium hydride. The syntheses are described in detail and characteri
ISSN:0022-152X
DOI:10.1002/jhet.5570100115
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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16. |
Reaction of 2‐aminobenzimidazole with bifunetional carboxylie acid derivatives. Formation of pyrimido[1,2‐a] benzimidazolones |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 71-75
A. W. Chow,
D. R. Jakas,
B. P. Trotter,
N. M. Hall,
J. R. E. Hoover,
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摘要:
Abstract2‐Aminobenzimidazole reacts with α,β‐unsaturated carboxylic acid chlorides or esters to give only pyrimido [1,2‐a] benzimidazol‐2‐(1H) ones. β‐Ethoxymethylenemalonie acid derivatives or β‐ketocarboxylic acid derivatives give only pyrimido [1,2‐a] benzimidazol‐4‐(1H)ones. Structural assignments based on nmr and chemical mani
ISSN:0022-152X
DOI:10.1002/jhet.5570100116
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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17. |
Synthesis of a potential camptothecin intermediate |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 77-78
Tetsuji Kametani,
Hiromitsu Takeda,
Fumio Satoh,
Seiichi Takano,
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摘要:
AbstractCondensation of dimethyl 1,2‐dihydro‐2‐oxopyridine‐4,6‐dicarboxylate (IIIb) with methyl acrylate yielded 1,2,3,5‐tetrahydro‐2,7‐dimethoxycarbonyl‐1,5‐dioxoindolizine (IV), which on hydrolysis and decarboxylation gave 1,2,3,5‐tetrahydro‐1,5‐dioxoindolizine‐7‐carboxylic acid (VI). Friedländer condensation of VI with 2‐aminobenzaldehyde, followed by esterification of the resulting oxoindolizino[1,2‐b]quinoline‐7‐carboxylic acid (VIIa), yielded a potential camptothecin intermediate 9,10‐dihydro‐7‐methoxycar
ISSN:0022-152X
DOI:10.1002/jhet.5570100117
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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18. |
5‐Substituted uraeils |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 79-83
D. M. Mulvey,
R. D. Babson,
S. Zawoiski,
M. A. Ryder,
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ISSN:0022-152X
DOI:10.1002/jhet.5570100118
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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19. |
Synthesis of 5,6‐dihydro‐6‐methoxynitidine and a practical preparation of nitidine chloride |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 85-88
Kwang‐Yuen Zee‐Cheng,
C. C. Cheng,
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ISSN:0022-152X
DOI:10.1002/jhet.5570100119
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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20. |
Benzo[b] furan‐2‐carboxylic acid and its congeners |
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Journal of Heterocyclic Chemistry,
Volume 10,
Issue 1,
1973,
Page 89-90
Francesco Fringuelli,
Aldo Taticchi,
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ISSN:0022-152X
DOI:10.1002/jhet.5570100120
出版商:Wiley‐Blackwell
年代:1973
数据来源: WILEY
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