Synthesis of Sitagliptin Phosphate by a NaBH4/ZnCl2-catalyzed Diastereoselective Reduction
Author:
Affiliation:
1. School of Perfume and Aroma Technology, Shanghai Institute of Technology
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/cl.150390
Reference12 articles.
1. (2R)-4-Oxo-4-[3-(Trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin- 7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine: A Potent, Orally Active Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes
2. First Generation Process for the Preparation of the DPP-IV Inhibitor Sitagliptin
3. Highly Efficient Asymmetric Synthesis of Sitagliptin
4. Direct Asymmetric Reductive Amination
5. Efficient and practical asymmetric synthesis of 1-tert-butyl 3-methyl (3R,4R)-4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine-1,3-dicarboxylate, a useful intermediate for the synthesis of nociceptin antagonists
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1. New dimensions in triazolo[4,3-a]pyrazine derivatives: The land of opportunity in organic and medicinal chemistry;Arabian Journal of Chemistry;2020-12
2. Sitagliptin;Retrosynthesis in the Manufacture of Generic Drugs;2020-11-09
3. Synthesis of ( R )‐3‐( tert ‐Butoxycarbonylamino)‐4‐(2,4,5‐trifluorophenyl)butanoic Acid, a Key Intermediate, and the Formal Synthesis of Sitagliptin Phosphate;Chemistry – An Asian Journal;2020-04-20
4. Reductive Amination in the Synthesis of Pharmaceuticals;Chemical Reviews;2019-10-21
5. A selective removal of the secondary hydroxy group from ortho-dithioacetal-substituted diarylmethanols;Beilstein Journal of Organic Chemistry;2018-05-29
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