Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cindy Klaus"'
Autor:
Cindy Klaus, Stephan Hammer
Publikováno v:
Trends in Chemistry. 4:363-366
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::763454d28e8a8dc76df9ff11a159cd8f
https://doi.org/10.1016/j.trechm.2022.03.002
https://doi.org/10.1016/j.trechm.2022.03.002
Autor:
Duncan Stuart Macdonald, Donald Hilvert, Cindy Klaus, Xavier Garrabou, Takahiro Mori, Rebecca Verez
Publikováno v:
Journal of the American Chemical Society. 142:10250-10254
Controlling regio- and stereoselectivity of aldol additions is generally challenging. Here we show that an artificial aldolase with high specificity for acetone as the aldol donor can be reengineered via single active site mutations to accept linear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a09e8bd946a64fbec8e052f7cd2914a1
https://doi.org/10.1021/jacs.0c02351
https://doi.org/10.1021/jacs.0c02351
Publikováno v:
Journal of the American Chemical Society (JACS), 2022, vol. 144, núm. 35, p. 15954-15968
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
instname
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
instname
The aerobic oxidation of alkenes to carbonyls is an important and challenging transformation in synthesis. Recently, a new P450-based enzyme (aMOx) has been evolved in the laboratory to directly oxidize styrenes to their corresponding aldehydes with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48688718cb0e63d8597b30edf2a36f50
http://hdl.handle.net/10256/21668
http://hdl.handle.net/10256/21668
Autor:
Cindy Klaus, Christian P. Bold, Karl-Heinz Altmann, J. Fernando Díaz, Jasmine Schürmann, Rafael Lombardi, Bernhard Pfeiffer, Daniel Lucena-Agell
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Organic Letters, 23 (6)
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Organic Letters, 23 (6)
5 p.-2 fig.-4 schem.-1 graph. abst.
Studies are described toward the synthesis of an oxazole-based analog of (−)-zampanolide (2). Construction of (−)-dactylolide analog 22 was achieved via alcohol 5 and acid 4 through esterification and Horn
Studies are described toward the synthesis of an oxazole-based analog of (−)-zampanolide (2). Construction of (−)-dactylolide analog 22 was achieved via alcohol 5 and acid 4 through esterification and Horn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4089ddaf840e1862256aef4d6e02130
http://hdl.handle.net/10261/236883
http://hdl.handle.net/10261/236883