Herein we report a practical protocol for the visible-lightinduced regiodivergent radical hydropyridylation of unactivated alkenes using pyridinium salts. This approach provides a unified synthetic platform to control the regioselectivity of the synthesis of linear or branched C4-alkylated pyridines. A remarkable selectivity switch from the antiMarkovnikov to the Markovnikov product can be achieved by the addition of tetrabutylammonium bromide. The versatility of this protocol is further demonstrated based on the late-stage functionalization in pharmaceuticals.11Nsciescopu
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim A general strategy for visible-light-enabled site-...
An efficient pyridylic C(sp3)−H functionalization has been developed through photocatalytic radical-...
The photocatalyzed ortho-selective migration on a pyridyl ring has been achieved for the site-select...
The intermolecular alkylation of pyridine units with simple alkenes has been achieved via a photored...
The site-selective C-H functionalization of heteroarenes is of considerable importance for streamlin...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
We report the photoredox alkylation of halopyridines using functionalized alkene and alkyne building...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimN-Alkenoxypyridinium salts have been used as syntho...
© 2019 American Chemical Society.A strategy for visible-light-induced site-selective C-H acylation o...
Metal-free, visible-light-induced site-selective heteroarylation of remote C(sp3)?H bonds has been a...
A one-pot umpolung method for the ring-opening pyridylation of unstrained cyclic amines was develope...
One of the main goals of modern synthesis is to develop distinct reaction pathways from identical st...
We report a photochemical method for the functionalization of pyridines with radicals derived from a...
© 2019 The Royal Society of Chemistry. Reported is a novel visible-light-enabled alkoxy radical ring...
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim A general strategy for visible-light-enabled site-...
An efficient pyridylic C(sp3)−H functionalization has been developed through photocatalytic radical-...
The photocatalyzed ortho-selective migration on a pyridyl ring has been achieved for the site-select...
The intermolecular alkylation of pyridine units with simple alkenes has been achieved via a photored...
The site-selective C-H functionalization of heteroarenes is of considerable importance for streamlin...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
We report the photoredox alkylation of halopyridines using functionalized alkene and alkyne building...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimN-Alkenoxypyridinium salts have been used as syntho...
© 2019 American Chemical Society.A strategy for visible-light-induced site-selective C-H acylation o...
Metal-free, visible-light-induced site-selective heteroarylation of remote C(sp3)?H bonds has been a...
A one-pot umpolung method for the ring-opening pyridylation of unstrained cyclic amines was develope...
One of the main goals of modern synthesis is to develop distinct reaction pathways from identical st...
We report a photochemical method for the functionalization of pyridines with radicals derived from a...
© 2019 The Royal Society of Chemistry. Reported is a novel visible-light-enabled alkoxy radical ring...
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim A general strategy for visible-light-enabled site-...
An efficient pyridylic C(sp3)−H functionalization has been developed through photocatalytic radical-...
The photocatalyzed ortho-selective migration on a pyridyl ring has been achieved for the site-select...