Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Petra Vojáčková"'
Publikováno v:
Nature. 616:84-89
Asymmetric transition-metal catalysis represents a powerful strategy for accessing enantiomerically enriched molecules. Here, we report a new approach for inducing enantioselectivity in transition-metal-catalyzed reactions that relies on neutral hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c74342506654dcd1e6947fb72bb971
https://doi.org/10.21203/rs.3.rs-1999100/v1
https://doi.org/10.21203/rs.3.rs-1999100/v1
Autor:
Judit E. Šponer, Dimitri Shcherbakov, Erik C. Böttger, Lucyna Michalska, Jakub Švenda, Jiří Šponer, Petra Vojáčková, Marek Nečas
Publikováno v:
Journal of the American Chemical Society. 142(16)
A stereoselective synthesis of the ribosome-binding antitumor antibiotic (-)-bactobolin A is reported. The presented approach makes effective use of (-)-quinic acid as a chiral pool starting material and substrate stereocontrol to establish the five
Publikováno v:
Organic letters. 19(4)
The first synthesis of cephalimysins B and C is reported. The route features a Ni(II)–diamine-catalyzed enantioselective conjugate addition of a densely substituted 3(2H)-furanone and an efficient dihydroxylation–lactonization sequence as key ste