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Nianxin Rong
Observed names:
Nian-Xin, RONG,
Rong, Nian-Xin,
Rong, Nianxin
Institution:
Shenzhen University of Advanced Technology
Observed institutions:
Nanchang University,
Liaocheng University,
Chinese Academy of Sciences,
Shenzhen Institutes of Advanced Technology,
Shenzhen University of Advanced Technology
ORCID:
0000-0001-8826-0525
Observed ORCID:
0000-0001-8826-0525
OpenAlex ID:
A5024880517
Asymmetric Hydrogenation of Racemic 2-Substituted Indoles via Dynamic Kinetic Resolution: An Easy Access to Chiral Indolines Bearing Vicinal Stereogenic Centers
2024
·
Nianxin Rong
, Ao Zhou
, et al.
·
Journal of the American Chemical Society
·
38
Highly selective production of propionic acid from lactic acid catalyzed by NaI
2020
·
Shengqin Liu
, Huan Feng
, et al.
·
Green Chemistry
·
37
Dynamic Kinetic Resolution-Based Asymmetric Transfer Hydrogenation of Racemic 2-Substituted Quinolines
2025
·
Ming-Rong Liang
, Xian Du
, et al.
·
Journal of the American Chemical Society
·
33
AIBN-Promoted Synthesis of Bibenzo[b][1,4]thiazines by the Condensation of 2,2′-Dithiodianiline with Methyl Aryl Ketones
2018
·
Xianqiang Huang
, Nianxin Rong
, et al.
·
Organic Letters
·
28
Catalyst-free synthesis of biodiesel precursors from biomass-based furfuryl alcohols in the presence of H 2 O and air
2019
·
Shengxiang Qin
, Teng Li
, et al.
·
Green Chemistry
·
20
Synthesis of Chiral Primary Amines via Enantioselective Reductive Amination: From Academia to Industry
2022
·
Xumu Zhang
, Qin Yin
, et al.
·
Synthesis
·
14
Radical induced disproportionation of alcohols assisted by iodide under acidic conditions
2021
·
Yang Peng
, Yang Huang
, et al.
·
Green Chemistry
·
13
Three pyrazole-3-carboxylic acid complexes as efficient solvent-free heterogeneous catalysts for C C bond formation
2017
·
Nianxin Rong
, Tiantian Qiu
, et al.
·
Inorganic Chemistry Communications
·
12
Asymmetric Transfer Hydrogenation of Stable NH Imines for the Synthesis of Enantiopure α‐Chiral Primary Amines
2024
·
Mangang Zhang
, Hui Li
, et al.
·
Chinese Journal of Chemistry
·
11
Enantioselective and Step-Economic Synthesis of the Chiral Amine Fragment in the Tyrosine Kinase Inhibitor Repotrectinib by Direct Asymmetric Reductive Amination under Batch and Flow
2023
·
Lei Xu
, Gang Wang
, et al.
·
Organic Process Research & Development
·
8
A practical route to 2-iodoanilines via the transition-metal-free and base-free decarboxylative iodination of anthranilic acids under oxygen
2021
·
Nianxin Rong
, Yongsheng Yuan
, et al.
·
Organic Chemistry Frontiers
·
7
Asymmetric hydrogenation of α-pyrrolyl terminal alkenes: An easy access to enantioenriched pyrroles bearing a C2 Me-substituted stereogenic center
2025
·
Ao Zhou
, Nianxin Rong
, et al.
·
Green Synthesis and Catalysis
·
4
CCDC 2321293: Experimental Crystal Structure Determination
2026
·
Li, Hui
, Nie, Zhiwen
, et al.
·
The Cambridge Structural Database
Palladium-catalyzed asymmetric annulation of phenols with 1,3-enynes via sequential hydroarylation–hydroalkoxylation
2026
·
Hui Li
, Zhiwen Nie
, et al.
·
Chinese Chemical Letters
Dynamic Kinetic Resolution-Based Asymmetric Hydrogenation of Pyridines
2026
·
Zhiwen Nie
, Nianxin Rong
, et al.
·
Journal of the American Chemical Society
CCDC 1055762: Experimental Crystal Structure Determination
2018
·
Jiang, Xiu-Yan
, Rong, Nian-Xin
, et al.
·
The Cambridge Structural Database
CCDC 1055760: Experimental Crystal Structure Determination
2018
·
Jiang, Xiu-Yan
, Rong, Nian-Xin
, et al.
·
The Cambridge Structural Database
CCDC 1055761: Experimental Crystal Structure Determination
2017
·
Rong, Nianxin
, Qiu, Tiantian
, et al.
·
The Cambridge Structural Database
CCDC 1475902: Experimental Crystal Structure Determination
2017
·
Xiu-Yan, JIANG
, Nian-Xin, RONG
, et al.
·
The Cambridge Structural Database
CCDC 1055221: Experimental Crystal Structure Determination
2017
·
Rong, Nianxin
, Qiu, Tiantian
, et al.
·
The Cambridge Structural Database
CCDC 1055763: Experimental Crystal Structure Determination
2017
·
Rong, Nianxin
, Qiu, Tiantian
, et al.
·
The Cambridge Structural Database
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Works count:
21
Citation count:
224
H-index:
9
I10-index:
9
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