Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniel Sowa Prendes"'
Autor:
Mario Martínez‐Mingo, Andrés García‐Viada, Daniel Sowa Prendes, Inés Alonso, Nuria Rodríguez, Ramón Gómez Arrayás, Juan C. Carretero
Publikováno v:
Angewandte Chemie International Edition. 61
The selective δ-C(sp3)−H acetoxylation of N-(SO2Py)-protected amino acid derivatives has been accomplished by using palladium-catalysis and PhI(OAc)2 (PIDA) as both terminal oxidant and acetoxy source. The distinct structural and electronic featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9b6088b04aab15ac3909340e412d06
https://doi.org/10.1002/anie.202209865
https://doi.org/10.1002/anie.202209865
Autor:
Mario, Martínez-Mingo, Andrés, García-Viada, Daniel Sowa, Prendes, Inés, Alonso, Nuria, Rodríguez, Ramón Gómez, Arrayás, Juan C, Carretero
Publikováno v:
Angewandte Chemie (International ed. in English). 61(47)
The selective δ-C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60c57dca33f8c00da7b92e9dd5150986
https://pubmed.ncbi.nlm.nih.gov/36177787
https://pubmed.ncbi.nlm.nih.gov/36177787
Publikováno v:
The Journal of Organic Chemistry
Ylide-substituted phosphines have been shown to be excellent ligands for C–N coupling reactions under mild reaction conditions. Here we report studies on the impact of the steric demand of the substituent in the ylide-backbone on the catalytic acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12af33d938e83dcf71eaca4654d99a7b
https://doi.org/10.1021/acs.joc.0c01771
https://doi.org/10.1021/acs.joc.0c01771
Autor:
Nardana Sivendran, Florian Belitz, Daniel Sowa Prendes, Ángel Manu Martínez, Rochus Schmid, Lukas J. Gooßen
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(9)
Trihalide salts were found to efficiently promote photochemical dediazotizing halogenations of diazonium salts. In contrast to classical Sandmeyer reactions, no metal catalysts are required to achieve high yields and outstanding selectivities for hal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0689670d0d7de721adf81fdd4923a68a
https://pubmed.ncbi.nlm.nih.gov/34911153
https://pubmed.ncbi.nlm.nih.gov/34911153