Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Felix Krätzschmar"'
Autor:
Alexander Breder, Felix Krätzschmar, Katharina Rode, Poorva Ramadas Narasimhamurthy, Rene Rieger
Publikováno v:
European Journal of Organic Chemistry
The facile synthesis of aminoallenes, accomplished by a selenium‐π‐acid‐catalyzed cross‐coupling of an N‐fluorinated sulfonimide with simple, non‐activated alkynes, is reported. Until now, aminoallenes were difficult to be accessed by cu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4047c7908dce3445487270f0a3f60a88
Publikováno v:
Angewandte Chemie. 130:2484-2488
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df8fe17bbf619c6e27fd7851ab365328
https://doi.org/10.1002/ange.201711599
https://doi.org/10.1002/ange.201711599
Publikováno v:
Organic Chemistry Frontiers. 3:314-318
An iodine(III)-mediated synthesis of substituted phenanthrenes from ortho-vinylated biaryl derivatives through highly 6-endo-trig selective oxidative intramolecular arene–alkene coupling is reported. The title method allows for the construction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bea14a85d9f7f28c7b666dcb6b766e0
https://doi.org/10.1039/c5qo00361j
https://doi.org/10.1039/c5qo00361j
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 21(19)
Oxidative Se-catalyzed C(sp3)-H bond acyloxylation has been used to construct a diverse array of isobenzofuranones from simple ortho-allyl benzoic acid derivatives. The synthetic procedure employs mild reaction conditions and gives high chemoselectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8d62cf10c444e34e012ceec30202097
https://pubmed.ncbi.nlm.nih.gov/25808950
https://pubmed.ncbi.nlm.nih.gov/25808950