Zobrazeno 1 - 10
of 232
pro vyhledávání: '"R. J. Stephenson"'
Autor:
Alexandra C. Sun, Daniel J. Steyer, Anthony R. Allen, Emory M. Payne, Robert T. Kennedy, Corey R. J. Stephenson
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-6 (2020)
Translating discovery scale vial-based batch reactions to continuous flow scale-up conditions is limited by significant time and resource constraints. Here, the authors report a photochemical droplet microfluidic platform, which enables high throughp
Externí odkaz:
https://doaj.org/article/aec33517a74540628771a347128e1c41
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
Arene dearomatization reactions allow chemists to rapidly build unique chemical architectures from largely available starting materials. Here, the authors show a photocatalytic carboamination/dearomatization cascade process leading to 1,4-cyclohexadi
Externí odkaz:
https://doaj.org/article/fab209fa1c37460da0791187c95c689d
Publikováno v:
Organic Process Research & Development. 27:399-408
Publikováno v:
The Journal of Organic Chemistry. 88:6281-6283
Autor:
Irene Bosque, Gabriel Magallanes, Mathilde Rigoulet, Markus D. Kärkäs, Corey R. J. Stephenson
Publikováno v:
ACS Central Science, Vol 3, Iss 6, Pp 621-628 (2017)
Externí odkaz:
https://doaj.org/article/80ad77a72ce941d1a384d43ca18d0d31
Publikováno v:
Org Lett
Detailed herein is the development of a photochemical intermolecular formal [3+2] cycloaddition between cyclopropylimines and substituted alkenes to generate aminocyclopentane derivatives. The Schiff base of the cyclopropylimine was designed to enabl
Publikováno v:
ACS Catalysis. 12:6729-6736
Autor:
Alexandra C. Sun, Daniel J. Steyer, Richard I. Robinson, Carol Ginsburg‐Moraff, Scott Plummer, Jinhai Gao, Joseph W. Tucker, Dirk Alpers, Corey R. J. Stephenson, Robert T. Kennedy
Publikováno v:
Angewandte Chemie International Edition.
Publikováno v:
J Am Chem Soc
Amines containing bridged bicyclic carbon skeletons are desirable building blocks for medicinal chemistry. Herein, we report the conversion of bicyclo[1.1.1]pentan-1-amines to a wide range of poly-substituted bicyclo[3.1.1]heptan-1-amines through a p
Publikováno v:
Angew Chem Int Ed Engl
The field of strain-driven, radical formal cycloadditions is experiencing a surge in activity motivated by a renaissance in free radical chemistry and growing demand for sp(3)-rich ring systems. The former has been driven in large part by the rise of