Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Marta Adeva"'
Autor:
Marta Adeva, Samreen K. Syed, Thomas B. Farb, Xin Zhou, Thomas James Beauchamp, David Andrew Coates, Francis S. Willard, Tamika D. Meredith, Susan L. Gackenheimer, Michael A. Statnick, Maria Angeles Martinez-Grau, Miguel A. Toledo, Brian A. Droz, James Ficorilli, Alexander M. Efanov, Gema Ruano, Over Cabrera, Todd M. Suter, Victoriano Molero, Krister Bokvist, David Gene Barrett
Publikováno v:
Endocrinology. 158:3859-3873
Incretin and insulin responses to nutrient loads are suppressed in persons with diabetes, resulting in decreased glycemic control. Agents including sulfonylureas and dipeptidyl peptidase-4 inhibitors (DPP4i) partially reverse these effects and provid
Autor:
Michael J. Coghlan, Rachel N. Richey, Javier Mendiola, Matthew W. Carson, Hannah Yu, Marta Adeva, Carmen Somoza, Scott A. May
Publikováno v:
Tetrahedron Letters. 49:1915-1918
A stereoselective method for the preparation of dibenzoxapine containing tetrasubstituted exocyclic E-alkenes has been developed. The key reaction involves an intramolecular cyclocarbopalladation of alkynes to form a vinylpalladium species and subseq
Publikováno v:
Tetrahedron Letters. 38:6893-6896
The synthesis of 1-(3,4,5-trimethoxyphenyl)-3-trialkylsiloxy-1,3-butadienes and their Diels-Alder reaction with selected dienophiles at room temperature is described. These aryldienes are useful building blocks for the synthesis of natural and pharma
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 28
The synthesis of 1-(3,4,5-trimethoxyphenyl)-3-trialkylsiloxy-1,3-butadienes and their Diels-Alder reaction with selected dienophiles at room temperature is described. These aryldienes are useful building blocks for the synthesis of natural and pharma
Autor:
Marta Adeva, Matthew W. Carson, Hannah Yu, Scott A. May, Carmen Somoza, Rachel N. Richey, Michael J. Coghlan, Javier Mendiola
Publikováno v:
ChemInform. 39
A stereoselective method for the preparation of dibenzoxapine containing tetrasubstituted exocyclic E-alkenes has been developed. The key reaction involves an intramolecular cyclocarbopalladation of alkynes to form a vinylpalladium species and subseq
Autor:
Heidi Sahagún, Marta Adeva, José Luis García Fernández, Miguel López-Lázaro, Suzanne Calderon, Esther Caballero, Manuel Medarde, Fernando Tomé, Maria Jesus Ayuso
Publikováno v:
ChemInform. 34
An array of 4-(aryl or indolyl)pyrrolo[3,4- c ]carbazole-1,3-diones (open analogues of indolocarbazole alkaloids), 10-(aryl or indolyl)pyrrolo[3,4- b ]carbazole-1,3-diones, and different derivatives have been prepared using a Diels–Alder plus Fisch
Publikováno v:
ChemInform. 31
Autor:
Manuel Medarde, Rafael Peláez-Lamamié de Clairac, Fernando Tomé, Esther Caballero, Marta Adeva, Heidi Sahagún
Publikováno v:
ChemInform. 31
Autor:
Rafael Peláez-Lamamié de Clairac, Marta Adeva, Esther Caballero, Heidi Sahagún, Fernando Tomé, and Manuel Medarde
Publikováno v:
The Journal of organic chemistry. 65(11)
The preparation of a range of open analogues of arcyriaflavin A is described. The synthetic approach is based on the use of perhydroisoindole-1,3,5-triones as key intermediates, which were obtained via Diels-Alder methodology using 1-aryl-3-siloxy-1,