Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ann Wens V. Silaire"'
Publikováno v:
Organic & Biomolecular Chemistry. 13:7915-7919
The synthesis of α- and α,β-functionalized azepenes and dehydropiperidines from readily prepared α-selenonyl eneformamides or enecarbamates has been achieved through Fe-catalyzed α-substitutive deselenonation, β-regioselective lithiation/trappi
Autor:
Ann Wens V. Silaire, Nathan Fox, Amir Alwali, Kayla Sincavage, Timothy K. Beng, Daniel P. Bassler
Publikováno v:
Organic & Biomolecular Chemistry. 13:8647-8651
The interception of carbolithiation-derived tertiary benzylic α-lithio piperidines with carbon electrophiles, under HMPA-mediated conditions, has led to the diastereoselective synthesis of vicinally functionalized piperidines bearing α-amino quater
Autor:
Ann Wens V. Silaire, Kayla Sincavage, Nathan Fox, Timothy K. Beng, Daniel P. Bassler, Amir Alwali
Publikováno v:
ChemInform. 46
The interception of carbolithiation-derived tertiary benzylic α-lithio piperidines with carbon electrophiles, under HMPA-mediated conditions, has led to the diastereoselective synthesis of vicinally functionalized piperidines bearing α-amino quater
Publikováno v:
ChemInform. 46
The synthesis of α- and α,β-functionalized azepenes and dehydropiperidines from readily prepared α-selenonyl eneformamides or enecarbamates has been achieved through Fe-catalyzed α-substitutive deselenonation, β-regioselective lithiation/trappi
Autor:
Amir Alwali, Ann Wens V. Silaire, Daniel P. Bassler, Oliver Beale, Timothy K. Beng, Laura Spence, Kayla Sincavage
Publikováno v:
ChemInform. 46
The synthesis of functionalized azepenes and piperidines bearing an α-cycloheptenone or benzotropone derivative has been accomplished through direct reductive cross-coupling of α-bromo eneformamides or enecarbamates with highly versatile α-bromo b