Prinessa Chellan
Soochow University (Suzhou)
6 Papers
2 Citations
Prinessa Chellan is an academic researcher from Soochow University (Suzhou). The author has contributed to research in topics: Catalysis & Aryl. The author has an hindex of 3, co-authored 6 publications. Previous affiliations of Prinessa Chellan include University of Cape Town.
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Papers
Thiosemicarbazone salicylaldiminato palladium(II)-catalyzed alkynylation couplings between arylboronic acids and alkynes or alkynyl carboxylic acids
TL;DR: In this article, an efficient catalytic system for the synthesis of unsymmetrical substituted alkynes via the thiosemicarbazone salicylaldiminato palladium(II)-catalyzed alkynylation couplings between arylboronic acids and alkynes was developed.
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Cyclometallated Pd(II) thiosemicarbazone complexes: new catalyst precursors for Suzuki-coupling reactions
TL;DR: In this paper, four tridentate [C,N,S] thiosemicarbazone Pd(II) complexes were applied as catalyst precursors for the Suzuki-Miyaura coupling of a variety of aryl halides and boronic acids.
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Cyclometallated Pd(II) Thiosemicarbazone Complexes: New Catalyst Precursors for Suzuki-Coupling Reactions.
TL;DR: In this paper, a ferrocene containing thiosemicarbazone complex is described as novel catalyst for the Suzuki-coupling of aryl bromides and p-chloronitrobenzene.
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Thiosemicarbazone Salicylaldiminato Palladium(II)-Catalyzed Alkynylation Couplings Between Arylboronic Acids and Alkynes or Alkynyl Carboxylic Acids.
TL;DR: Tridentate Pd(II) salicylaldiminato-thiosemicarbazone complexes can efficiently catalyze the alkynylation couplings of a variety of arylboronic acids with alkynes or carboxylic acids under mild conditions as mentioned in this paper.
1
Thiosemicarbazone Salicylaldiminato‐Palladium(II)‐Catalyzed Mizoroki—Heck Reactions.
TL;DR: In this paper, a novel catalyst is presented for the Mizoroki-Heck coupling reaction of a wide range of electron-rich and electron-deficient aryl halides with terminal olefins.