has been cited by the following article(s):
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[1]
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Synthesising complex chiral amines through resolution-racemisation-recycle
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2022 |
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[2]
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Biaryl diphosphine ligands and their ruthenium complexes: Preparation and use for catalytic hydrogenation of ketones
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2020 |
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[3]
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Application of Chiral Sulfinamides into Formation and Reduction of Sulfinylketimines to Obtain Valuable α‐Chiral Primary Amines
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2020 |
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[4]
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Σύνθεση καινοτόμων παραγώγων της ριβαστιγμίνης για την αντιμετώπιση γνωσιακών δυσλειτουργιών
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2018 |
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[5]
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A Practical and Efficient Stereoselective Synthesis of (S)‐Rivastigmine and (R)‐Rivastigmine
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ChemistrySelect,
2018 |
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[6]
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利斯的明中间体含量及 ee 值的 RP-HPLC 法测定
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郑州大学学报（医学版）,
2015 |
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[7]
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一种改进的卡巴拉汀制备工艺
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中国药科大学学报,
2015 |
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[8]
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Discontinuous two step flow synthesis of m-aminoacetophenone
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Green Processing and Synthesis,
2014 |
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[9]
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ENANTIOMERIC SEPARATION OF AMINES BY GAS CHROMATOGRAPHY USING DERIVATIZED CYCLODEXTRINS AS STATIONARY PHASES
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2013 |
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[10]
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Industrial Scale-Up of Enantioselective Hydrogenation for the Asymmetric Synthesis of Rivastigmine
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Organic Process Research & Development,
2013 |
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[11]
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Synthesis Design of ‘Rivastigmine’-A Potent Therapeutic Agent forAlzheimer’s disease using Retrosynthetic Analysis
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Journal of Chemical and Pharmaceutical Research,
2013 |
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[12]
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Enantioselective reduction of ketoxime ethers with borane–oxazaborolidines and synthesis of the key intermediate leading to ( S)-rivastigmine
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Tetrahedron: Asymmetry,
2012 |
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[13]
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A novel asymmetric synthesis of cinacalcet hydrochloride
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Beilstein journal of organic chemistry,
2012 |
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[14]
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Enantioselective reduction of ketoxime ethers with borane–oxazaborolidines and synthesis of the key intermediate leading to (S)-rivastigmine
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Tetrahedron: Asymmetry,
2012 |
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[15]
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Synthesis design of 'Rivastigmine'—A potent therapeutic agent for Alzheimer's disease using retrosynthetic analysis
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J. Chem. Pharm. Res,
2012 |
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[1]
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Biaryl diphosphine ligands and their ruthenium complexes: Preparation and use for catalytic hydrogenation of ketones
Inorganica Chimica Acta,
2020
DOI:10.1016/j.ica.2020.119850
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[2]
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Application of Chiral Sulfinamides into Formation and Reduction of Sulfinylketimines to Obtain Valuable α-Chiral Primary Amines
European Journal of Organic Chemistry,
2020
DOI:10.1002/ejoc.202000608
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[3]
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A Practical and Efficient Stereoselective Synthesis of (S)-Rivastigmine and (R)-Rivastigmine
ChemistrySelect,
2018
DOI:10.1002/slct.201703032
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[4]
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Industrial Scale-Up of Enantioselective Hydrogenation for the Asymmetric Synthesis of Rivastigmine
Organic Process Research & Development,
2013
DOI:10.1021/op3003147
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[5]
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A novel asymmetric synthesis of cinacalcet hydrochloride
Beilstein Journal of Organic Chemistry,
2012
DOI:10.3762/bjoc.8.158
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[6]
|
Enantioselective reduction of ketoxime ethers with borane–oxazaborolidines and synthesis of the key intermediate leading to (S)-rivastigmine
Tetrahedron: Asymmetry,
2012
DOI:10.1016/j.tetasy.2012.05.008
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