Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kai Dr. Thede"'
Autor:
Metin Akbaba, Uwe Thuss, Kai Dr. Thede, Gunter Karig, Jörg Keldenich, Friederike Stoll, Hans-Christian Militzer, Ingo Flamme, Mario Jeske, Jens-Kerim Ergüden, Felix Oehme, Ingo Hartung, Hartmut Beck
Publikováno v:
ChemMedChem. 13:981-981
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ddaf8ac9825bcf1279a19664c77a512
https://doi.org/10.1002/cmdc.201800275
https://doi.org/10.1002/cmdc.201800275
Publikováno v:
ChemInform. 36
Rocaglaols are natural products exhibiting a range of biological activities. A new synthetic method for the α-arylation of ketones allows for the synthesis of previously inaccessible rocaglaol derivatives. The key sequence consists of a previously u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b24626887070c141b8c289eb76a415f
https://doi.org/10.1002/chin.200535055
https://doi.org/10.1002/chin.200535055
Publikováno v:
Organic letters. 6(24)
An intramolecular hydroxy epoxide opening was used to access the cyclopenta[b]benzofuran ring system of the natural product rocaglaol (2). Our route allowed the stereocontrolled preparation of the rocaglaol derivative (+/-)-(1S*,3S*,3aR*,8bS*)-3b. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9121a97efc63f6c1b58083ff91b0d186
https://pubmed.ncbi.nlm.nih.gov/15548084
https://pubmed.ncbi.nlm.nih.gov/15548084