Sulfoximines, a ubiquitous class of structural motifs, are widely present in bioactive molecules and functional materials that have received considerable attention from modern organic chemistry, pharmaceutical industries, and materials science. Sulfoximines have proved to be an effective directing group for C–H functionalization which was widely investigated for the synthesis of cyclic sulfoximines. Within the last decade, great progress has been achieved in the synthesis of cyclic sulfoximines. Thus, this review highlights the recent advances in the synthesis of cyclic sulfoximines via the C–H activation strategy and is classified based on the substrate types
The presented thesis covers three research topics concerning sulfur chemistry. The main focus of thi...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
This work focuses on new synthetic methods and bioactivities of sulfoximines and pentafluorosulfanyl...
The synthesis of sulfoximines has been studied since the late 1940s but their application in academi...
This thesis describes the development of a general synthetic approach for the diastereoselective syn...
Medicinally relevant sulfoximines are accessed from C–S coupling of sulfonimidates and commercially ...
The ever-increasing prevalence of sulfoximine derivatives in drug discovery programmes has brought a...
This thesis focuses closely on the latest advancements in the synthesis of sulfur(VI) analogues, nam...
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a ...
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
In this thesis, the development of iron-catalyzed imidation reactions of sulfoxides to access NH sul...
Compared to sulfone-based drugs, sulfoximine- and sulfilimine-based bioactive compounds are not so c...
In the early 1950s, Whitehead and Bentley reported the discovery of sulfoximines. From then on, more...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
The presented thesis covers three research topics concerning sulfur chemistry. The main focus of thi...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
This work focuses on new synthetic methods and bioactivities of sulfoximines and pentafluorosulfanyl...
The synthesis of sulfoximines has been studied since the late 1940s but their application in academi...
This thesis describes the development of a general synthetic approach for the diastereoselective syn...
Medicinally relevant sulfoximines are accessed from C–S coupling of sulfonimidates and commercially ...
The ever-increasing prevalence of sulfoximine derivatives in drug discovery programmes has brought a...
This thesis focuses closely on the latest advancements in the synthesis of sulfur(VI) analogues, nam...
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a ...
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
In this thesis, the development of iron-catalyzed imidation reactions of sulfoxides to access NH sul...
Compared to sulfone-based drugs, sulfoximine- and sulfilimine-based bioactive compounds are not so c...
In the early 1950s, Whitehead and Bentley reported the discovery of sulfoximines. From then on, more...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
The presented thesis covers three research topics concerning sulfur chemistry. The main focus of thi...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
This work focuses on new synthetic methods and bioactivities of sulfoximines and pentafluorosulfanyl...