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1. |
The chemistry of cyclic enaminoketones. III. Synthesis of bi‐ and tricyclic enaminoketones from enamine esters and nitriles |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 151-159
A. I. Meyers,
A. H. Reine,
J. C. Sircar,
K. B. Rao,
S. Singh,
H. Weidmann,
M. Fitzpatrick,
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摘要:
AbstractThe cyclization of enamines derived from β‐aminoesters and β‐aminonitriles into bi‐ and tricyclic enaminoketones (6,9,13and24) has been investigated. The enamines derived from aminonitriles cyclize smoothly with magnesium perchlorate in benzene or toluene, whereas the enamines derived from aminoesters cyclize spontaneously during their formation. The scope and limitation of this process is di
ISSN:0022-152X
DOI:10.1002/jhet.5570050201
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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2. |
The synthesis of oximes containing the ferroin group |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 161-164
Francis H. Case,
Patrick J. Mcmenamin,
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摘要:
AbstractA series of oximes of substituted 2‐pyridylmethyl and phenyl ketones has been prepared. These all contain the ferroin group (NCCN). The 4‐substituted pyridyl‐syn‐methyl and phenyl ketoximes form che
ISSN:0022-152X
DOI:10.1002/jhet.5570050202
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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3. |
Synthesis of possible metabolites of chlorpromazine. II.3‐, 8‐ and 9‐hydroxychlorpromazine |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 165-177
Edward A. Nodiff,
Noriichi Oda,
Takanori Hayazaki,
Shuichiro Ina,
Toshiyuki Ito,
Sansei Nishibe,
Taisei Ueda,
Kenji Suzuki,
Martin Hausman,
Albert A. Manian,
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摘要:
AbstractThe title compounds have been prepared as analytical standards for the identification of chlorpromazine metabolites in biological materials. Unequivocal structural proof of key compounds was accomplished by using at least two unrelated syntheses for each one. Resistance of some phenothiazines to preparation via classic Smiles rearrangement is discussed. More examples are offered of halogen‐induced Smiles rearrangement. A rare example of phenothiazine polymorphism is presente
ISSN:0022-152X
DOI:10.1002/jhet.5570050203
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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4. |
Ring closure reactions with nitriles. I. Formation of pyrrolo [2,1‐c] [1,2,4]benzothiadiazines and pyrrolo[1,2‐a] quinazolines |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 179-183
Stanley C. Bell,
George Conklin,
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摘要:
AbstractPyrrolo[2,1‐c][1,2,4]benzothiadiazines have been prepared from the reactions ofo‐amino‐benzenesulfonamides with γ‐cyanopropionaldehydes. Pyrrolo[1,2‐a]quinazolines have been prepared from the reaction of anthranilamides with either γ‐cyanopropionaldehyde or succinic anhydride. The cyclization of a 4‐oxo‐2‐quinazolinepropionic acid has produced a pyrrolo‐[1,2‐a]quinazoline and the isomeric py
ISSN:0022-152X
DOI:10.1002/jhet.5570050204
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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5. |
Ring closure reactions with nitriles. II. Formation of pyrrolo[1,2‐a] quinazolines and thiazolo[3,2‐a] quinazolines |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 185-190
Stanley C. Bell,
Peter H. L. Wei,
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摘要:
Abstract2‐Quinazolinepropionic acids have been obtained from the reactions of potassium cyanide witho‐carboxy‐ oro‐acyl‐3‐chloropropionanilides. Some of these compounds have been cyclized to pyrrolo [1,2‐a] quinazolines. The reaction of ano‐carbethoxy‐2‐chloroacetanilide with potassium thiocyanate formed a 2‐quinazolinylthioacetic acid, which was cyclized to a thiazolo‐[3,2‐a]quinazoline. A mechanism is presented for the for
ISSN:0022-152X
DOI:10.1002/jhet.5570050205
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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6. |
Synthesis and spectral properties of some 1,2‐dithienylethenes and 1‐thieny1‐4‐phenylbutadienes |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 191-194
E. Campaigne,
William L. Fleming,
Alan Dinner,
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摘要:
AbstractA total of seven thiophene derivatives not previously reported have been preparedviathe Knoevenagel condensation of an activated methylthiophene and a heterocyclic or aromatic aldehyde. The principal peaks in the ultraviolet and visible absorption spectra as well as some nuclear magnetic resonance data are reported for these compounds.
ISSN:0022-152X
DOI:10.1002/jhet.5570050206
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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7. |
Pyrazoles. II. Reactions of 1‐methyl‐5‐amino‐4‐pyrazolecarboxamide and nitrous acid introduction of a nitro group at position 5 in the payrazole ring |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 195-197
C. C. Cheng,
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摘要:
AbstractAddition of sodium nitrite to a mixture of hydrochloric acid and 1‐methyl‐5‐amino‐4‐pyrazolecarboxamide, at either high or low temperature, yielded 1‐methyl‐4‐hydroxypyrazolo‐[3,4‐d]‐v‐triazine. On the other hand, addition of hydrochloric acid to an aqueous mixture of sodium nitrite and 1‐methyl‐5‐amino‐4‐pyrazolecarboxamide gave, at high temperature (˜ 100°), 1‐methyl‐5‐nitro‐4‐pyrazolecarboxylic acid and at low temperature (˜ 0°), 1
ISSN:0022-152X
DOI:10.1002/jhet.5570050207
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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8. |
Picrylamino‐substituted heterocycles. III. 1,2,4‐triazoles |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 199-203
Michael D. Coburn,
Thomas E. Jackson,
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摘要:
AbstractThis paper describes the synthesis of various picryl‐and picrylamino‐substituted 1,2,4‐triazoles and 3,3′‐bi‐1,2,4‐triazolyls. These compounds were prepared by condensing the appropriate 1,2,4‐triazole or amino‐1,2,4‐triazole with a picryl halide. The proton n.m.r. spectra, crystal densities, thermal stabilities, and drop‐weight impact sensitivities of the resulting comp
ISSN:0022-152X
DOI:10.1002/jhet.5570050208
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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9. |
A direct, stereoselective synthesis of optically active conhydrines |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 205-209
Gabor Fodor,
Eberhard Bauerschmidt,
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摘要:
Abstract2‐Pyridylethylcarbinol (I) has been resolved and the antipodes hydrogenated as free bases. The (+) form gave (+) conhydrine (II) while the (‐) form afforded the levorotatory base stereoselectively with minor contamination of the other epimer. Hydrogenation ofracemicI as well as of 2‐pyridyl ethyl ketone in acid solution led formerly to the mixture of both race
ISSN:0022-152X
DOI:10.1002/jhet.5570050209
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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10. |
Reaction of certain isocyanates with azomethines. Evidence for a new heterocyclic adduct |
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Journal of Heterocyclic Chemistry,
Volume 5,
Issue 2,
1968,
Page 211-215
John P. Chupp,
Helen K. Landwehr,
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摘要:
AbstractThe preparation of triazinone (I) from certain isocyanates andN‐alkyl azomethines was found to proceed easily without catalyst, particularly in refluxing chlorobenzene. The physical and chemical properties, including n.m.r. spectra of the oily triazinones, are contrasted with the newly discovered solid adducts arising from low temperature reaction of azomethine and chlorophenyl isocyanates. From stoichiometry of the reaction, elemental analysis, molecular weight of the products, and spectral analyses, the new materials (II) were found to incorporate two isocyanate and three azomethine moieties in their molecular make‐up. The relative merits are considered for assigning II a molecular structure arising from a complex between a four and six‐membered ring (III, IV) versus a ten‐membered ring system (V, V
ISSN:0022-152X
DOI:10.1002/jhet.5570050210
出版商:Wiley‐Blackwell
年代:1968
数据来源: WILEY
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