Zobrazeno 1 - 10
of 128
pro vyhledávání: '"ALFONS L. BAUMSTARK"'
Autor:
Saajid Z. Azhar, Andrew C. Clay, Hadrian Mendoza, Glenda M. Duffek, Nicole A. Brown, Jianmei Cui, Anand B. Shah, Hayley B. Arrowood, Alfons L. Baumstark, Beatrice A. Edjah, Amy N. Hockstedler
Publikováno v:
Heterocyclic Communications. 23:125-131
A series of chalcones 1–12 were converted to pyrazolines (1Pi–12Pi) by reaction with phenylhydrazine followed by DDQ oxidation to produce the corresponding pyrazoles (1Pz–12Pz). Three 1-phenyl-3-t-butyl-5-arylpyrazoles (13Pz–15Pz) were synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a5a4883ca9a99341be05d77c173f4e7
https://doi.org/10.1515/hc-2017-0034
https://doi.org/10.1515/hc-2017-0034
Autor:
Alfons L. Baumstark
Publikováno v:
Heterocyclic Communications. 23:133-135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fd32e8bc2f90276e860d5154209fe11
https://doi.org/10.1515/hc-2017-0113
https://doi.org/10.1515/hc-2017-0113
Autor:
Ronald Shanderson, Stephanie Ross, Patrick Gaulden, Hector Argueta-Gonzalez, Beatrice A. Edjah, Julia Dave, Jiayo Yu, Alfons L. Baumstark
Publikováno v:
Heterocyclic Communications. 21:279-283
A series of 3,5-diarylisoxazoles (1–9) underwent reaction with N-bromosuccinimide in acetic acid to yield the corresponding 3.5-diaryl-4-bromoisoxazoles (1Br–9Br) in low to moderate yield. The X-ray structure of 3-(4-chlorophenyl)-5-phenyl-4-brom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca4538c2adc66f5eb49ee008ddcd800d
https://doi.org/10.1515/hc-2015-0111
https://doi.org/10.1515/hc-2015-0111
Publikováno v:
Heterocyclic Communications. 21:47-53
The reaction of dimethyldioxirane (1) with excess 1,3-cyclohexadiene (2a) and 1,3-cyclooctadiene (2b) in dried acetone yielded the corresponding monoepoxides in excellent yield. Second-order rate constants for monoepoxidation were determined using UV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff29bc1565718395db9672368963abc4
https://doi.org/10.1515/hc-2014-0211
https://doi.org/10.1515/hc-2014-0211
Publikováno v:
hc. 18:75-78
Kinetic data for the reaction of dimethyldioxirane (1) with a series of acyclic, aliphatic conjugated dienes 2a–f are reported. Monoepoxidation is the preferred process and the monoepoxides are formed in high yield as long as the dienes are in exce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eae0a9515cce885839956934afcc496f
https://doi.org/10.1515/hc-2011-0125
https://doi.org/10.1515/hc-2011-0125