1448439-01-7Relevant academic research and scientific papers
Copper-catalyzed enantioselective alkene carboetherification for the synthesis of saturated six-membered cyclic ethers
Berhane, Ilyas A.,Burde, Ameya S.,Chemler, Sherry R.,Kennedy-Ellis, Jonathan J.,Zurek, Eva
supporting information, p. 10099 - 10102 (2021/10/06)
The enantioselective copper-catalyzed oxidative coupling of alkenols with styrenes for the construction of dihydropyrans, isochromans, pyrans and morpholines is reported. A concise formal synthesis of a σ1receptor ligand using this alkene carbo
Copper-Catalyzed Enantioselective Hydroalkoxylation of Alkenols for the Synthesis of Cyclic Ethers
Chen, Dake,Berhane, Ilyas A.,Chemler, Sherry R.
supporting information, p. 7409 - 7414 (2020/06/29)
The copper-catalyzed enantioselective intramolecular hydroalkoxylation of unactivated alkenes for the synthesis of tetrahydrofurans, phthalans, isochromans, and morpholines from 4- and 5-alkenols is reported. The substrate scope is complementary to existing enantioselective alkene hydroalkoxylations and is broad with respect to substrate backbone and alkene substitution. The asymmetric induction and isotopic labeling studies support a polar/radical mechanism involving enantioselective oxycupration followed by C-[Cu] homolysis and hydrogen atom transfer. Synthesis of the antifungal insecticide furametpyr was accomplished.
Synthesis, spectral characterization and biological screening of n-substituted derivatives of n-(1-Hydroxy-2-methylpropan-2-yl)benzenesulfonamide
Aziz-ur-Rehman,Abbas, Nadia,Abbasi, Muhammad Athar,Khalid, Hira,Khan, Khalid Mohammed,Ashraf, Muhammad,Ahmad, Irshad,Ejaz, Syeda Abida
, p. 3289 - 3293 (2013/05/09)
In the present study, a series of N-substituted derivative of N-(1-hydroxy-2-methylpropan-2-yl)benzenesulfonamide was synthesized. Firstly, the reaction of 2-amino-2-methyl propan-1-ol (1) with benzenesulfonyl chloride (2) yielded N-(1-hydroxy-2-methylpro
