A concise enantioselective synthesis of l-(−)-733,061 and (2S,3S)-methyl 3-aminopiperidine-2-carboxylate using catalytic enantioselective aza-Henry reaction as key step-Reference-Cited by-同舟云学术

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A concise enantioselective synthesis of l-(−)-733,061 and (2S,3S)-methyl 3-aminopiperidine-2-carboxylate using catalytic enantioselective aza-Henry reaction as key step

Published:2011-04 Issue:14 Volume:67 Page:2536-2541
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kumaraswamy Gullapalli,Pitchaiah Arigala

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference39 articles.

1. A major piperidine alkaloid from Microcos Philippinensis

2. Antibacterial Activity of Juliflorine Isolated fromProsopis juliflora

3. 1-Aza Sugars, Apparent Transition State Analogues of Equatorial Glycoside Formation/Cleavage

4. Asymmetric routes to substituted piperidines

5. Saturated nitrogen heterocycles

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1. Catalytic asymmetric synthesis of 1,2-diamines;Chemical Society Reviews;2024

2. Applications in Organic Synthesis;Asymmetric Organo‐Metal Catalysis;2021-11-02

3. Synthesis of the Neurokinin 1 Receptor Antagonist (+)-L-733,060 by Jacobsen’s Hydrolytic Kinetic Resolution;Russian Journal of Organic Chemistry;2020-12

4. The Stereoselective Nitro-Mannich Reaction in the Synthesis of Active Pharmaceutical Ingredients and Other Biologically Active Compounds;Frontiers in Chemistry;2020-01-28

5. Total Synthesis of 2‐(2‐Ketoalkyl)‐piperidine Alkaloids (+)‐ Pelletierine, (+)‐Haloxynine and (‐)‐ N ‐Methyl‐pelletierine via Regioselective Wacker Oxidation;ChemistrySelect;2019-08-05

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