Practical, efficient, and general methods for the diversification of N-heterocycles have been a recurrent goal in chemical synthesis due to the ubiquitous influence of these motifs within bioactive frameworks. Here, we describe a direct, catalytic, and selective functionalization of azines via silylium activation. Our catalyst design enables mild conditions and a remarkable functional group tolerance in a one-pot setup
Strong and confined imidodiphosphorimidate (IDPi) catalysts enable highly enantioselective substitut...
Based on our group’s previous study on chemoselective partial reduction of silyl-protected sugars an...
Previously held under moratorium in Chemistry Department (GSK) from 17/06/2020 until 22/11/2022New m...
Previously held under moratorium in Chemistry department (GSK) from 24/05/2018 until 18/06/2021.The ...
Nitrogen-rich heterocyclic compounds have had a profound impact on human health, as these chemical m...
A method for the catalytic generation of functionalized aryl alkali metals is reported. These highly...
One of the fundamental problems facing modern society is our dependence on fossil fuels. Critically,...
We describe, for the first time, a highly regioselective hydrosilylation of propargylic amines. The ...
A Brønsted acid catalyzed intramolecular cyclization of N-Cbz-protected diazoketones, derived from α...
This thesis describes the research conducted towards the overall goal of developing new synthetic or...
Tris(pentafluorophenyl)borane-catalyzed silylative reduction of pyridines has been developed giving ...
Trimethylsilyl chloride is an efficient activating agent for azines in isocyanide-based reactions, w...
Amino boronate based bifiinctional molecules have the potential to be powerful catalysts. Herein, a...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
Thesis advisor: Kian L. TanThesis advisor: Shih-Yuan LiuChapter 1. In the Tan laboratory, we develop...
Strong and confined imidodiphosphorimidate (IDPi) catalysts enable highly enantioselective substitut...
Based on our group’s previous study on chemoselective partial reduction of silyl-protected sugars an...
Previously held under moratorium in Chemistry Department (GSK) from 17/06/2020 until 22/11/2022New m...
Previously held under moratorium in Chemistry department (GSK) from 24/05/2018 until 18/06/2021.The ...
Nitrogen-rich heterocyclic compounds have had a profound impact on human health, as these chemical m...
A method for the catalytic generation of functionalized aryl alkali metals is reported. These highly...
One of the fundamental problems facing modern society is our dependence on fossil fuels. Critically,...
We describe, for the first time, a highly regioselective hydrosilylation of propargylic amines. The ...
A Brønsted acid catalyzed intramolecular cyclization of N-Cbz-protected diazoketones, derived from α...
This thesis describes the research conducted towards the overall goal of developing new synthetic or...
Tris(pentafluorophenyl)borane-catalyzed silylative reduction of pyridines has been developed giving ...
Trimethylsilyl chloride is an efficient activating agent for azines in isocyanide-based reactions, w...
Amino boronate based bifiinctional molecules have the potential to be powerful catalysts. Herein, a...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
Thesis advisor: Kian L. TanThesis advisor: Shih-Yuan LiuChapter 1. In the Tan laboratory, we develop...
Strong and confined imidodiphosphorimidate (IDPi) catalysts enable highly enantioselective substitut...
Based on our group’s previous study on chemoselective partial reduction of silyl-protected sugars an...
Previously held under moratorium in Chemistry Department (GSK) from 17/06/2020 until 22/11/2022New m...