Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Patrik Kolar"'
Autor:
Philippe Rocca-Serra, Jacques E. Remacle, Amanda Collis, Susan K. Gregurick, Mary Maxon, Dawn Field, Nicola Perrin, Susanna-Assunta Sansone, Bela Tiwari, John Wilbanks, Eugene Kolker, Alexis-Michel Mugabushaka, Patrik Kolar, Siân Millard, Timothy F. Booth, Mark Thorley, Peter Dukes, Chris F. Taylor, Karen Kennedy, Karin A. Remington
Publikováno v:
Science. 326:234-236
Development of high-throughput genomic and postgenomic technologies has caused a change in approaches to data handling and processing ( 1 ). One biological sample might be used to generate many kinds of “big” data in parallel, such as genome sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6d5d15615d10bb0795434cc12a1b811
https://doi.org/10.1126/science.1180598
https://doi.org/10.1126/science.1180598
Publikováno v:
ResearcherID
Chiral aldehydes 4a,b, obtained by the ozonolysis of the corresponding N,N′-fumaroylbis[(S)-proline esters] 3 react in the presence of lanthanoid chelate complexes Eu(fod)3 or Eu(hfc)3 with silyloxydienes 7 or 12 to give δ-lactones 10 or dihydro-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88616c07eec6d4cc0e97e11ce018696e
https://doi.org/10.1002/(sici)1099-0690(199901)1999:1<329::aid-ejoc329>3.0.co
https://doi.org/10.1002/(sici)1099-0690(199901)1999:1<329::aid-ejoc329>3.0.co
Publikováno v:
Journal of Heterocyclic Chemistry. 34:1067-1098
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c9806957d4ac48b2476aba05f17e456
https://doi.org/10.1002/jhet.5570340401
https://doi.org/10.1002/jhet.5570340401
Autor:
Miha Tišler, Patrik Kolar
Publikováno v:
Journal of Heterocyclic Chemistry. 32:141-144
Substituted pyrrolo[1,2-a]imidazoles and imidazo[1,2-a]imidazoles are prepared in a simple one pot reaction sequence from esters of heterocyclic or aromatic α-amino acids. The reaction involves condensation with acetoine followed by cyclization with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b166771be035dd13f034661154fbb6f0
https://doi.org/10.1002/jhet.5570320123
https://doi.org/10.1002/jhet.5570320123
Autor:
Miha Tišler, Patrik Kolar
Publikováno v:
Synthetic Communications. 24:1887-1893
A new simple synthesis of substituted pyrroles from alkyl, aryl or heteroaryl substituted α-amino acids is described. Esters of α-amino acids are first reacted with dimethyl acetylenedicarboxylate and in the in situ formed enamines are there-after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7db622c86271ba02a2dc3fad1dc0928f
https://doi.org/10.1080/00397919408010197
https://doi.org/10.1080/00397919408010197
Publikováno v:
ChemInform. 23
From the corresponding heterocyclic amino acids 2 and 9a the heterocyclic systems imidazo[1,5-a]pyridine (3) and imidazo[1,5-a]quinoline (10) are easily accessible. From compound 7 the tricyclic system 11 was prepared and from compound 17a a pyridyl-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc286fd5b58260c0e434f895938c16a2
https://doi.org/10.1002/chin.199211183
https://doi.org/10.1002/chin.199211183
Autor:
Miha Tišler, Patrik Kolar
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c9cb2dc64d5e30f70ae18b46348d788
https://doi.org/10.1002/chin.199146209
https://doi.org/10.1002/chin.199146209
Autor:
Miha Tišler, Patrik Kolar
Publikováno v:
ChemInform. 25
From some alkyl heteroarylglycinates and dicarbonyl compounds various heterocyclic systems are easily accessible. Transformations are described which lead to imidazo[1,5-α]pyridines, heteroaryl-substituted pyrroles, pyrido[1,2-α]pyrazines, pyrido[1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5eac14398e48b7399fe12325bc1931a
https://doi.org/10.1002/chin.199416066
https://doi.org/10.1002/chin.199416066
Autor:
Miha Tišler, Patrik Kolar
Publikováno v:
ChemInform. 25
A new simple synthesis of substituted pyrroles from alkyl, aryl or heteroaryl substituted α-amino acids is described. Esters of α-amino acids are first reacted with dimethyl acetylenedicarboxylate and in the in situ formed enamines are there-after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::868ef8a505c0b128ab9660e17fa61074
https://doi.org/10.1002/chin.199447142
https://doi.org/10.1002/chin.199447142
Autor:
Miha Tišler, Patrik Kolar
Publikováno v:
ChemInform. 26
Substituted pyrrolo[1,2-a]imidazoles and imidazo[1,2-a]imidazoles are prepared in a simple one pot reaction sequence from esters of heterocyclic or aromatic α-amino acids. The reaction involves condensation with acetoine followed by cyclization with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07441ed341a89e4ccfa2a2077ea3322a
https://doi.org/10.1002/chin.199530141
https://doi.org/10.1002/chin.199530141