Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kaitie C. Cartwright"'
Autor:
Kaitie C. Cartwright, Jon A. Tunge
Publikováno v:
Chemical Science. 11:8167-8175
A dual catalytic decarboxylative allylation and benzylation method for the construction of new C(sp3)–C(sp3) bonds between readily available carboxylic acids and functionally diverse carbonate electrophiles has been developed. The new process is mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1623f740ee744359dcadaad80d65bfc
https://doi.org/10.1039/d0sc02609c
https://doi.org/10.1039/d0sc02609c
Publikováno v:
European Journal of Organic Chemistry. 2020:1245-1258
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::327a673eb912d75e7d4d870d50867f1c
https://doi.org/10.1002/ejoc.201901170
https://doi.org/10.1002/ejoc.201901170
Publikováno v:
The Journal of Organic Chemistry. 84:12553-12561
Organic molecules bearing acetoxy moieties are important functionalities in natural products, drugs, and agricultural chemicals. Synthesis of such molecules via transition metal-catalyzed C-O bond formation can be achieved in the presence of a carefu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29300cbd912aedb5adfdccc98656a896
https://doi.org/10.1021/acs.joc.9b02092
https://doi.org/10.1021/acs.joc.9b02092
Autor:
Kaitie C, Cartwright, Jon A, Tunge
Publikováno v:
Chemical Science
A dual catalytic decarboxylative allylation and benzylation method for the construction of new C(sp3)–C(sp3) bonds between readily available carboxylic acids and functionally diverse carbonate electrophiles has been developed. The new process is mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccf8895cd316d5b4c4cf9729b93bce79
https://pubmed.ncbi.nlm.nih.gov/34094175
https://pubmed.ncbi.nlm.nih.gov/34094175
Autor:
Kaitie C. Cartwright, Jon A. Tunge
Publikováno v:
ACS Catalysis. 8:11801-11806
A dual-catalytic strategy for the synthesis of enamides and enecarbamates directly from easily accessible and inexpensive amino acids has been realized. This mild and efficient protocol makes use of an organic photoredox catalyst and a cobaloxime cat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e0e7cb37647a8e757ab47c24a1cfab3
https://doi.org/10.1021/acscatal.8b03282
https://doi.org/10.1021/acscatal.8b03282
Publikováno v:
The Journal of organic chemistry. 84(5)
Decarboxylative elimination of easily accessible N-acyl amino acids to provide enamide and enecarbamate building blocks has been realized through the combination of an organophotoredox catalyst and copper acetate as the terminal oxidant. This operati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::051dadca6269767949de0a532cd1d675
https://pubmed.ncbi.nlm.nih.gov/30785754
https://pubmed.ncbi.nlm.nih.gov/30785754
Publikováno v:
European journal of organic chemistry. 2016(20)
Aminodecarboxylation of unactivated alkyl carboxylic acids has been accomplished utilizing an organic photocatalyst. This operationally simple reaction utilizes readily available carboxylic acids to chemoselectively generate reactive alkyl intermedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10844be5bac3ad08f39b934d5fb044ad
https://pubmed.ncbi.nlm.nih.gov/28936118
https://pubmed.ncbi.nlm.nih.gov/28936118
Publikováno v:
European Journal of Organic Chemistry. 2020:1186-1186
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c61106ddeeec75fce9fee0e974aec4c
https://doi.org/10.1002/ejoc.201901910
https://doi.org/10.1002/ejoc.201901910
Publikováno v:
ChemInform. 47
Aminodecarboxylation of unactivated alkyl carboxylic acids has been accomplished utilizing an organic photocatalyst. This operationally simple reaction utilizes readily available carboxylic acids to chemoselectively generate reactive alkyl intermedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb7d14a31b23f6dae42a16e92a32a8d4
https://doi.org/10.1002/chin.201648061
https://doi.org/10.1002/chin.201648061