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Yana Fu
Researcher at East China Normal University
Publications - 5
Citations - 180
Yana Fu is an academic researcher from East China Normal University. The author has contributed to research in topics: Intramolecular force & Catalysis. The author has an hindex of 2, co-authored 4 publications receiving 164 citations.
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Efficient access to 1,4-benzothiazine: palladium-catalyzed double C-S bond formation using Na2S2O3 as sulfurating reagent.
TL;DR: A novel Pd-catalyzed double C-S bond formation coupling reaction has been developed that provides an efficient method for the synthesis of substituted 1,4-benzothiazine derivates, which are structural elements of numerous bioactivity molecules rendering this protocol attractive to both synthetic and medicinal chemistry.
Journal ArticleDOI
Palladium-catalyzed intramolecular reductive cross-coupling of Csp2-Csp3 bond formation.
TL;DR: A Pd-catalyzed efficient reductive cross-coupling reaction without metallic reductant to construct a Csp(2) -Csp(3) bond has been reported.
Journal ArticleDOI
Efficient Access to 1,4‐Benzothiazine: Palladium‐Catalyzed Double C—S Bond Formation Using Na2S2O3 as Sulfurating Reagent.
TL;DR: In this article, a Pd-catalyzed double C-S bond formation coupling reaction has been developed, in which Na2S2O3 was used as sulfurating reagent in metal-calyzed reactions, providing an efficient method for the synthesis of substituted 1,4-benzothiazine derivates.
Journal ArticleDOI
Palladium-Catalyzed Intramolecular Reductive Cross-Coupling of Csp2—Csp3 Bond Formation.
TL;DR: An efficient Pd-catalyzed reductive intramolecular cross-coupling of bis-iodo substrates of type (I) is developed to give good yields of indolines (II).
Journal ArticleDOI
λ3-Iodane/Lewis Acid Mediated Intramolecular Cross-Nucleophile Coupling of β-Amino Acrylates: Chemodivergent Syntheses of Indole Alkaloidal Frameworks.
Zeng-Xiu Sun,Shilin Xue,Yining Zhang,Shiyang Xin,Ran Guo,Xiaowei Shi,Yana Fu,Huicai Guo,Yi Liu,Lei Wang +9 more
TL;DR: An unprecedented intramolecular cross-nucleophile coupling strategy of indole tethered β-amino acrylates using a catalyst system combining λ3-iodanes and Lewis acids to achieve the chemodivergent synthesis of three unique alkaloid skeletons is reported.