Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bastien Cacherat"'
Publikováno v:
Angewandte Chemie. 133:17348-17355
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b560d0042cf354c2c3acb7e77c64641
https://doi.org/10.1002/ange.202103269
https://doi.org/10.1002/ange.202103269
Publikováno v:
Natural product reports. 39(1)
Covering: 2015 to 2020The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fa5bb9569c50dcb7dbfb514acd41461a
https://pubmed.ncbi.nlm.nih.gov/34263890
https://pubmed.ncbi.nlm.nih.gov/34263890
Publikováno v:
Angewandte Chemie (International Ed. in English)
Angewandte Chemie International Edition
Angewandte Chemie. International Edition, 60 (31)
Angewandte Chemie International Edition
Angewandte Chemie. International Edition, 60 (31)
We report an efficient and broadly applicable palladium‐catalyzed iodination of inexpensive and abundant aryl and vinyl carboxylic acids via in situ activation to the acid chloride and formation of a phosphonium salt. The use of 1‐iodobutane as i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d29ca13dba91cf75c871a1dcc484464
https://pubmed.ncbi.nlm.nih.gov/34013616
https://pubmed.ncbi.nlm.nih.gov/34013616
Publikováno v:
Angewandte Chemie International Edition. 56:13377-13381
A catalytic pinacol-type reductive rearrangement reaction of internal 1,2-diols is reported herein. Several scaffolds not usually amenable to pinacol-type reactions, such as aliphatic secondary-secondary diols, undergo the transformation well without
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adb388ab52e9e9e878d91d7b51eef844
https://doi.org/10.1002/anie.201704936
https://doi.org/10.1002/anie.201704936
Publikováno v:
Nature chemistry. 9(11)
The synthesis of carboxylic acid derivatives from unsaturated hydrocarbons is an important process for the preparation of polymers, pharmaceuticals, cosmetics and agrochemicals. Despite its industrial relevance, the traditional Reppe-type carbonylati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26a113035a5a72d70f304527916ac27f
https://pubmed.ncbi.nlm.nih.gov/29064496
https://pubmed.ncbi.nlm.nih.gov/29064496
Publikováno v:
ACS Catalysis, 5 (11)
We demonstrate that a simple Co(III)-complex can efficiently catalyze the cleavage of unstrained C–C bonds via the β-carbon elimination of secondary and tertiary alcohols bearing a directing group. The cobalt-aryl intermediate generated under the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dc15de62f29c0f84929858445acffdd
