Yinghong Zhu

Zhejiang University of Technology

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Chunan Ma

Zhejiang University of Technology

Wanli Chen

Chinese Academy of Sciences

Weimin Mo

Zhejiang University of Technology

Xiangliang Pan

Zhejiang University of Technology

Zhanfei He

Zhejiang University of Technology

Zhiquan Shen

Beike Biotechnology (China)

Jun Ling

Zhejiang University

Xiaoming Zheng

Jinan University

Daoyong Zhang

Zhejiang University

Jieni Feng

Guangzhou University of Chinese Medicine

Cooperative Institutions

Zhejiang University of Technology

Zhejiang University

Chinese Academy of Sciences

University of Chinese Academy of Sciences

Guangzhou Medical University

Third Affiliated Hospital of Guangzhou Medical University

Hangzhou Academy of Agricultural Sciences

Hangzhou Xixi hospital

University of Science and Technology of China

Huazhong University of Science and Technology

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The Correlation of Family Resilience with Sleep Quality and Depression of Parents of Children with Epilepsy

Journal of Pediatric Nursing (2020)

Peipei Liu Ping Yin Yinghong Zhu Shan Zhang Gui-Mei Sheng

Depression

Resilience

10.1016/j.pedn.2020.07.016

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Citations (27)

4,4-Dichlorotricyclo[5.4.0.0^3,5]undeca-7,9,11-triene

Acta Crystallographica Section E Structure Reports Online (2008)

Wan-Li Chen Guosheng Chen Yinghong Zhu Weimin Mo

The title compound, C11H10Cl2, is a useful intermediate for the synthesis of 1H-cyclopropa[b]naphthalene. Strain in the molecule is evidenced by the fact that the cyclohexane ring is essentially planar and nearly coplanar with the benzene ring [dihedral angle 1.87 (18)°], and the cyclopropyl ring is almost perpendicular to the cyclohexane ring [dihedral angle 70.99 (12)°]. The molecules are loosely connected into one-dimensional chains by intermolecular Cl⋯Cl interactions with a distance of 3.571 (1) Å. The centroid-to-centroid distance between stacked benzene rings is ca 5.89 Å, indicating that no π–π stacking exists in the crystal structure.

Dihedral angle

10.1107/s160053680801831x

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Et3N-Promoted Tandem Cyclization of Bromomaleimides with Active Methylene Compounds: An Efficient Synthesis of cis-3,4-Dihydropyrrolidine-2,5-diones

Synlett (2019)

Mengyao Li Yinghong Zhu Haibin Wang Wanli Chen

The Et3N-promoted tandem cyclization of bromomaleimides with active methylene compounds is presented, providing an efficient method for the synthesis of cis-3,4-dihydropyrrolidine-2,5-diones in moderate to good yields under mild conditions.

Tandem

Methylene

10.1055/s-0039-1690098

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Citations (3)

The effect of black carbon on the chemical degradability of PCB1 via TENAX desorption technology from the perspective of adsorption states

Chemosphere (2021)

Weijian Xu Jin Zhang Yutao Shen Hao Yu KeZhen Chen

Tenax

Degradation

10.1016/j.chemosphere.2021.131583

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Citations (9)

Et3N-promoted sequential reactions for the synthesis of 6H-benzo[c]chromenes

ARKIVOC (2011)

Wan-Li Chen Jiao Li Yinghong Zhu Wei Hu Weimin Mo

An interesting Et 3 N-promoted sequential reaction consisting of propargyl-allenyl isomerizations, intramolecular [4+2] cycloaddition and aromatization has been developed, providing a facile method for synthesis of 6H-benzo[c]chromenes under mild conditions in moderate yields.

10.3998/ark.5550190.0013.602

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Citations (2)

AgOTf-catalyzed cyclization of enynals or enynones with amines: an efficient synthesis of 1,2,4-trisubstituted pyrroles and 2,3,5-trisubstituted furans

ARKIVOC (2011)

Wan-Li Chen Jiao Li Yinghong Zhu Lu-Ting Ye Wei Hu

AgOTf-catalyzed amino-cyclization of 2-(1-alkynyl)-2-alken-1-als or 2-(1-alkynyl)-2-alken-1ones is presented, providing an efficient method for synthesis of 1,2,4-trisubstituted pyrroles or 2,3,5-trisubstituted furans with an arylamino-group function respectively under mild conditions in moderate yields.

10.3998/ark.5550190.0012.928

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Citations (23)

Ring‐opening polymerization of 1‐methyltrimethylene carbonate by rare earth initiators

Journal of Polymer Science Part A Polymer Chemistry (2010)

Jun Ling Yongbo Dai Yinghong Zhu Weilin Sun Zhiquan Shen

Abstract Ring‐opening polymerization of 1‐methyltrimethylene carbonate (MTMC) initiated by highly active single‐component rare earth tris(2,6‐di‐ tert ‐butyl‐4‐methylphenolate)s [Ln(OAr) 3 , Ln = La, Dy, Y] or yttrium isopropoxide [Y(O i Pr) 3 ] is reported for the first time. PolyMTMC ( M w = 8.4 × 10 4 , molecular weight distributions = 1.5) initiated by La(OAr) 3 at [MTMC]/[initiator] = 1000 was obtained with the yield over 99% in toluene within 1 h at 30 °C. Random and block copolymers of MTMC with ε‐caprolactone (CL), 2,2‐dimethyltrimethylene carbonate (DTC) or polyethylene glycol (PEG) including poly(MTMC‐ r ‐CL), poly(MTMC‐ b ‐CL), poly(MTMC‐ r ‐DTC), poly(MTMC‐ b ‐DTC), and poly(MTMC‐ b ‐PEG‐ b ‐MTMC) were synthesized. The differential scanning calorimetry results show that thermal behaviors of the polymers sensitively depend on their compositions and chain structures. Furthermore, the measurements of 1 H‐ 1 H COSY and density functional theory calculation are applied to investigate the mechanism. The polymerization of MTMC takes place according to a coordination‐insertion mechanism, and the ring is opened via acyl‐oxygen bond cleavage resulting in a LnO active center. There exist two ring‐opening modes of MTMC in which mode b , breaking the CH 2 OCO bond, is the major pathway. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3807–3815, 2010

Trimethylene carbonate

10.1002/pola.24166

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Citations (26)

Palladium-Catalyzed Intramolecular Cyclization of 2-Iodobenzamides: An Efficient Synthesis of 3-Acyl Isoindolin-1-ones and 3-Hydroxy-3-acylisoindolin-1-ones

Synlett (2013)

Wanli Chen Yinghong Zhu Lina Jin Xiaoji Cao Lebin Zheng

Palladium-catalyzed intramolecular cyclization of 2-iodobenzamides with a 2-oxoethyl function group on the nitrogen atom moiety is presented, providing an efficient method for the synthesis of 3-acyl isoindolin-1-ones and 3-hydroxy-3-acylisoindolin-1-ones under mild conditions in moderate yields.

Moiety

Nitrogen atom

10.1055/s-0033-1339449

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Citations (12)

ChemInform Abstract: Copper‐Catalyzed Tandem Reactions of 2‐Iodobenzamides with Sodium Azide: An Efficient Synthesis of [1,2,3]Triazolo[1,5‐a][1,4]‐benzodiazepin‐6(5H)‐ones.

ChemInform (2015)

Wanli Chen Haitao Li Xiaoling Gu Yinghong Zhu

Abstract The title compounds are efficiently obtained by reaction of 2‐iodobenzamides with a propargyl group on the nitrogen atom moiety and sodium azide under mild reaction conditions.

Sodium azide

Tandem

10.1002/chin.201533218

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Active anaerobic methane oxidation in the groundwater table fluctuation zone of rice paddies

Water Research (2024)

Zhanfei He Jiaquan Shen Yinghong Zhu Jingxun Gao Daoyong Zhang

Paddy field

Table (database)

10.1016/j.watres.2024.121802

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Citations (3)