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1. |
Oxo‐ and imino‐functionalized 1,2‐oxazetidines. An overview |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 579-591
Dietrich Moderhack,
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摘要:
AbstractThis review article describes syntheses and reactions of 1,2‐oxazetidines that have an oxo or (substituted) imino group attached to either C‐3 or C‐4. The rare case of a bifunctional derivative is also treated. In a final chapter, spectroscopic properties are sur
ISSN:0022-152X
DOI:10.1002/jhet.5570300301
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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2. |
Facile synthesis of 5,6,7,8‐tetrahydropyrido[2,1‐b]purin‐10‐one |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 593-595
Takeshi Kuroda,
Fumio Suzuki,
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摘要:
AbstractA convenient synthesis of a new heterocycle, 5,6,7,8‐tetrahydropyrido[2,1‐b]purin‐10‐one1was described. 4‐Amino‐N‐(5‐chloropentanoyl)‐5‐imidazolecarboxamide3awas successively cyclized to1with polyphosphoric acid at 150°. Methylation of1under basic condition proceeded selectively atN‐1 to affo
ISSN:0022-152X
DOI:10.1002/jhet.5570300302
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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3. |
A convenient synthesis of 3,4‐dihydro‐2‐methyl‐3‐oxo‐2H‐1,4‐benzoxazine‐2‐carboxylic acids and 3,4‐dihydro‐2‐methyl‐3‐oxo‐2H‐pyrido[3,2‐b]‐1, 4‐oxazine‐2‐carboxylic acid |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 597-602
Elizabeta Suhadolc,
UroŠ Urleb,
Urša Žbontar,
Danijel Kikelj,
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摘要:
AbstractA convenient one pot synthesis of ethyl 3,4‐dihydro‐2‐methyl‐3‐oxo‐2H‐1,4‐benzoxazine‐2‐carboxylates and 3,4‐dihydro‐2‐methyl‐3‐oxo‐2H‐pyrido[3,2‐b]‐1,4‐oxazine‐2‐carboxylates and their conversion into th
ISSN:0022-152X
DOI:10.1002/jhet.5570300303
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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4. |
A new method for the synthesis of 6H,11H‐indolo[3,2‐c]‐isoquinolin‐5‐ones/thiones and their reactions |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 603-609
Shivayogi P. Hiremath,
Ananda R. Saundane,
B. H. M. Mruthyunjayaswamy,
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摘要:
AbstractThe synthesis of 8‐substituted and unsubstituted 6H,11H‐indolo[3,2‐c]isoquinolin‐5‐ones/thiones3a‐cand4a‐cand their derivativesviz, ethyl (8‐substituted‐6H,11H‐indolo[3,2‐c]isoquinolin‐5‐on‐6‐yl)acetates5a‐c, (8‐substituted‐6H,11H‐indolo[3,2‐c]isoquinolin‐5‐on‐6‐yl)acetyl hydrazides6a‐c, 3,5‐disubstituted‐pyrazoles7a‐cand8a‐c, 3‐substituted‐pyrazol‐5‐ones9a‐cand 5‐(8‐substituted‐6H,11H‐indolo[3,2‐c]isoquinolin‐5‐on‐6‐yl)methyl‐1,3,4‐oxadiazole‐2‐thiones10a‐c, also ethyl (8‐substituted‐11H‐indolo[3,2‐c]isoquinolin‐5‐ylthio)ace‐tates11a‐c, (8‐substituted‐11Hindolo[3,2‐c]isoquinolin‐5‐ylthio)acetyl hydrazides12a‐c, 3,5‐disubstituted‐pyrazoles13a‐cand14a‐c, 3‐substitu
ISSN:0022-152X
DOI:10.1002/jhet.5570300304
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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5. |
Identification of a 4H‐benz[f]indole by‐product from the friedel‐crafts‐based synthesis of benzoylpyrrole calcium channel activators |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 611-615
Edward W. Huber,
Robert J. Barbuch,
Christopher R. Dalton,
John M. Kane,
Nelson L. Velayo,
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摘要:
Abstract9,9a‐Dihydro‐2,9a‐dimethyl‐4‐oxo‐4H‐benz[f]indole‐3‐carboxylic acid, methyl ester was formed in varying amounts from the Friedel‐Crafts‐based synthesis of benzoylpyrrole calcium channel activators. The structure of this by‐product was determined using two‐dimensional long‐range1H‐13C heteronuclear correlated
ISSN:0022-152X
DOI:10.1002/jhet.5570300305
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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6. |
The reaction of pyrroles with trimethylhalosilanes‐dialkyl sulfoxides |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 617-621
Franco Bellesia,
Franco Ghelfi,
Romano Grandi,
Ugo Maria Pagnoni,
Adriano Pinetti,
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摘要:
AbstractPyrroles are powerful nucleophiles in the reaction with dialkyl sulfoxides and trimethylchlorosilane (TMCS) or trimethylbromosilane (TMBS), affording sulfonium salts or halo derivatives, generally in good yields.
ISSN:0022-152X
DOI:10.1002/jhet.5570300306
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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7. |
9,9‐diphenyl‐1,9,10,10a‐tetrahydro‐2H‐phenaleno[1,9‐bc]pyrans |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 623-626
John R. Beswick,
W. David Cotterill,
Muhammad Iqbal,
Robert Livingstone,
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摘要:
AbstractReaction between some naphtho[2,1‐b]pyrans and 1,1‐diphenylethene affords 9,9‐diphenyl‐1,9,10,10a‐tetrahydro‐2H‐phenaleno[
ISSN:0022-152X
DOI:10.1002/jhet.5570300307
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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8. |
Unusual reaction of 1,8‐diazabicyelo‐[5.4.0]undec‐7‐ene with diethyl maleate |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 627-629
Michel Perbost,
Marc Lucas,
Claude Chavis,
Jean‐Louis Imbach,
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摘要:
AbstractMichael addition of DBU on diethyl maleate and subsequent cyclization of the adduct afforded a tricyclic derivative which was susceptible to react further with a second molecule of unsaturated diester.
ISSN:0022-152X
DOI:10.1002/jhet.5570300308
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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9. |
A convenient synthesis ofcis‐4‐(sulfomethyl)‐piperidine‐2‐carboxylic acid: NMR assignment |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 631-635
Ahmed El Hadri,
GÉRard Leclerc,
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摘要:
Abstractcis‐4‐(Sulfomethyl)piperidine‐2‐carboxylic acid was obtained in 22% overall yield from 4‐(hydroxymethyl)‐pyridineviatheo‐silylN‐oxide and trimethylsilylcyanide. Thecisconfiguration of5was unambiguously assigned by 200 MHz1H nmr and c
ISSN:0022-152X
DOI:10.1002/jhet.5570300309
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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10. |
Conformational study on indoline compounds. Structures of 2‐phenyl‐3‐arylimino‐3H‐indole 1‐Oxide, 1,2‐dihydro‐2‐phenyl‐2‐benzyl‐ and 2‐tert‐Butyl‐3‐phenylimino‐3H‐indole 1‐oxyls |
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Journal of Heterocyclic Chemistry,
Volume 30,
Issue 3,
1993,
Page 637-642
Corrado Rizzoli,
Paolo Sgarabotto,
Franco Ugozzoli,
Patricia Carloni,
Elisabetta Damiani,
Lucedio Greci,
Pierluigi Stipa,
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摘要:
AbstractReacting 1‐hydroxy‐2‐phenylindole with nitrosobenzene, 2‐phenyl‐3‐phenylimino‐3H‐indole 1‐oxide(1)is produced in only one of the two possible diastereomers. The latter reacts withtert‐butylmagnesium chloride and benzylmagnesium chloride giving, after oxidation, the corresponding aminoxyls which show the same configuration of the phenylimino group at C‐3 as in1. This has been demonstrated by means of nmr spectros‐copy and X‐ray crystal structure and represents an unexpecte
ISSN:0022-152X
DOI:10.1002/jhet.5570300310
出版商:Wiley‐Blackwell
年代:1993
数据来源: WILEY
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