Dan Yuan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Dan Yuan has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Ke Yang
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology School of Petrochemical Engineering Changzhou University Changzhou Jiangsu China
4 shared publications - Chong Liu
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
2 shared publications - Haibo Ge
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
2 shared publications - Bin-Dong Li
School of Chemistry and Chemical Engineering Nanjing University of Science and Technology Nanjing China
1 shared publication - Faith Herington
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
1 shared publication - Faith Herington
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
1 shared publication
Latest Publications
- Open Access
Metal-Free C(sp3)–S Bond Cleavage of Thioethers to Selectively Access Aryl Aldehydes and Dithioacetals
Metal-free C(sp3)–S bond cleavage of thioethers was achieved using NCS as a critical additive. A wide range of arylmethyl thioethers were successfully transformed into aryl aldehydes with satisfactory yields in chloroform. Meanwhile, employing fluorobenzene as the solvent enables the selective formation of dithioacetals from arylmethyl thioethers, achieving moderate to good yields. Notably, dithioacetals were first prepared through a metal-free C(sp3)–S bond cleavage and subsequent thioacetalization process. Furthermore, these simple and efficient approaches also provide complementary strategies for accessing important aryl aldehydes and dithioacetals.
Open AccessMetal-Free C(sp3)–S Bond Cleavage of Thioethers to Selectively Access Aryl Aldehydes and Dithioacetals
Metal-free C(sp3)–S bond cleavage of thioethers was achieved using NCS as a critical additive. A wide range of arylmethyl thioethers were successfully transformed into aryl aldehydes with satisfactory yields in chloroform. Meanwhile, employing fluorobenzene as the solvent enables the selective formation of dithioacetals from arylmethyl thioethers, achieving moderate to good yields. Notably, dithioacetals were first prepared through a metal-free C(sp3)–S bond cleavage and subsequent thioacetalization process. Furthermore, these simple and efficient approaches also provide complementary strategies for accessing important aryl aldehydes and dithioacetals.
- Open Access
Recent Advances in the Synthesis of Benzo[d]isothiazol-3(2H)-One and Benzo[e][1,3]Thiazin-4-One Derivatives
Benzo[d]isothiazol-3(2H)-one and benzo[e][1,3]thiazin-4-one derivatives, as significant sulfur- and nitrogen-containing heterocyclic compounds, are prevalent in natural products, pharmaceuticals, and food items. In recent years, a variety of innovative synthetic methodologies for these compounds have been developed. In this review, we will comprehensively introduce the major advances in the synthesis of benzo[d]isothiazol-3(2H)-one and benzo[e][1,3]thiazin-4-one derivatives via both intramolecular and intermolecular pathways from 2012 to the present.
Open AccessRecent Advances in the Synthesis of Benzo[d]isothiazol-3(2H)-One and Benzo[e][1,3]Thiazin-4-One Derivatives
Benzo[d]isothiazol-3(2H)-one and benzo[e][1,3]thiazin-4-one derivatives, as significant sulfur- and nitrogen-containing heterocyclic compounds, are prevalent in natural products, pharmaceuticals, and food items. In recent years, a variety of innovative synthetic methodologies for these compounds have been developed. In this review, we will comprehensively introduce the major advances in the synthesis of benzo[d]isothiazol-3(2H)-one and benzo[e][1,3]thiazin-4-one derivatives via both intramolecular and intermolecular pathways from 2012 to the present.
- Open Access
Palladium-Catalyzed Cascade Reactions for Synthesis of Heterocycles Initiated by C(sp3)–H Functionalization
Heterocycles are widely present in natural products, pharmaceuticals, and organic functional materials. In heterocycle synthesis, Pd-catalyzed cascade C–H functionalization has been regarded as one of the most powerful approaches due to its advantages in terms of high atom efficiency and readily available starting materials. In this review, we will briefly introduce the major advances in palladium-catalyzed cascade C(sp3)–H activation and annulation for constructing different types of heterocycles through inter- and intramolecular pathways from 2010 to 2023.
Open AccessPalladium-Catalyzed Cascade Reactions for Synthesis of Heterocycles Initiated by C(sp3)–H Functionalization
Heterocycles are widely present in natural products, pharmaceuticals, and organic functional materials. In heterocycle synthesis, Pd-catalyzed cascade C–H functionalization has been regarded as one of the most powerful approaches due to its advantages in terms of high atom efficiency and readily available starting materials. In this review, we will briefly introduce the major advances in palladium-catalyzed cascade C(sp3)–H activation and annulation for constructing different types of heterocycles through inter- and intramolecular pathways from 2010 to 2023.
- Open Access
Selective Oxidation of Benzo[d]isothiazol-3(2H)-Ones Enabled by Selectfluor
A metal-free and Selectfluor-mediated selective oxidation reaction of benzo[d]isothiazol-3(2H)-ones in aqueous media is presented. This novel strategy provides a facile, green, and efficient approach to access important benzo[d]isothiazol-3(2H)-one-1-oxides with excellent yields and high tolerance to various functional groups. Furthermore, the purification of benzoisothiazol-3-one-1-oxides does not rely on column chromatography. Moreover, the preparation of saccharine derivatives has been achieved through sequential, double oxidation reactions in a one-pot aqueous media.
Open AccessSelective Oxidation of Benzo[d]isothiazol-3(2H)-Ones Enabled by Selectfluor
A metal-free and Selectfluor-mediated selective oxidation reaction of benzo[d]isothiazol-3(2H)-ones in aqueous media is presented. This novel strategy provides a facile, green, and efficient approach to access important benzo[d]isothiazol-3(2H)-one-1-oxides with excellent yields and high tolerance to various functional groups. Furthermore, the purification of benzoisothiazol-3-one-1-oxides does not rely on column chromatography. Moreover, the preparation of saccharine derivatives has been achieved through sequential, double oxidation reactions in a one-pot aqueous media.