Zobrazeno 1 - 10
of 248
pro vyhledávání: '"Karl Anker Joergensen"'
Autor:
Danny Kaare Bech Joergensen, Karl Anker Joergensen, Alicia Monleon, Stefania Vergura, Pernille H. Poulsen
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b15b1bca294b4daa7caf9e6e93a58ac7
https://doi.org/10.1002/chin.201646137
https://doi.org/10.1002/chin.201646137
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adb0aaaee513ab1e4ae92c27115f52bf
https://doi.org/10.1002/chin.201640051
https://doi.org/10.1002/chin.201640051
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d7de3c4a278190e10f514af956ca2bc
https://doi.org/10.1002/chin.201640024
https://doi.org/10.1002/chin.201640024
Publikováno v:
ChemInform. 47
affording highly substituted cyclopentanes with up to four stereocenters in high yields and selectivities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27e94720753b6e04bc5c026a850a3bb8
https://doi.org/10.1002/chin.201637052
https://doi.org/10.1002/chin.201637052
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f8e84cd3e48bbcc5492fb818616b7c4
https://doi.org/10.1002/chin.201626277
https://doi.org/10.1002/chin.201626277
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::051896405fe1267535d915a0941f00cb
https://doi.org/10.1002/chin.201624115
https://doi.org/10.1002/chin.201624115
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea5e7a343dc6a6f5e871856842a11330
https://doi.org/10.1002/chin.201621166
https://doi.org/10.1002/chin.201621166
Publikováno v:
ChemInform. 47
An asymmetric Diels—Alder reaction of cyclopentenone (I) with a variety of activated 1,2-disubstituted and trisubstituted ethylenes is presented in the presence of the organocatalyst (ORG) and propionic acid as co-catalyst to furnish chiral multifu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b9a030e7a376b480a6979deae3a5d0a
https://doi.org/10.1002/chin.201612023
https://doi.org/10.1002/chin.201612023
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::557b2b4f175baf5bfea1cfaeb7e76028
https://doi.org/10.1002/chin.201602056
https://doi.org/10.1002/chin.201602056
Publikováno v:
ChemInform. 47
The enantioselective reaction of bromides (I) and (VI) with unsaturated aldehydes (II) followed by reduction or acetalization of intermediate aldehydes gives rise to alcohols (III) or acetals (VIII), which are readily converted into dihydropyran deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82444fcace062e93a75c7be5820eec17
https://doi.org/10.1002/chin.201601142
https://doi.org/10.1002/chin.201601142