Zobrazeno 1 - 4
of 4
pro vyhledávání: '"R. S. Childress"'
Publikováno v:
The Journal of Organic Chemistry. 63:144-151
A tandem demethoxycarbonylation-Michael addition reaction has been developed as a synthetic route to highly functionalized five- and six-membered oxygen heterocycles. Methyl esters, activated toward decarboxylation by a C-2 ethoxycarbonyl group and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76b9683d727c91462cd8c51f5c322b70
https://doi.org/10.1021/jo971600s
https://doi.org/10.1021/jo971600s
Autor:
R. S. Childress, R. A. Bunce
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b189f2d61853ad4bfe52031dbb3f756
https://doi.org/10.1002/chin.199618100
https://doi.org/10.1002/chin.199618100
Autor:
R. A. Bunce, R. S. Childress
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01661e3d9f5f233c9f81b82df0b54146
https://doi.org/10.1002/chin.199704110
https://doi.org/10.1002/chin.199704110
Publikováno v:
ChemInform. 29
A tandem demethoxycarbonylation-Michael addition reaction has been developed as a synthetic route to highly functionalized five- and six-membered oxygen heterocycles. Methyl esters, activated toward decarboxylation by a C-2 ethoxycarbonyl group and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61a44657b06d502df73484efece883fa
https://doi.org/10.1002/chin.199824042
https://doi.org/10.1002/chin.199824042