Diastereoselective sulfonate-directed carbonyl reduction of γ-keto-sulfonates-Reference-Cited by-同舟云学术

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Diastereoselective sulfonate-directed carbonyl reduction of γ-keto-sulfonates

Published:2019-05 Issue:19 Volume:60 Page:1313-1316
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

McLaughlin Noel,Duffy Colm,Alletto Francesco,Ravelli Andrea,Lancianesi Stefano,Gillick-Healy Malachi,Adamo Mauro F.A.

Funder

Science Foundation Ireland

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones

2. Asymmetric synthesis of chiral N-(1-methylbenzyl)aminophosphines

3. Around and beyond Cram's Rule

4. Diastereofacial selection in nucleophilic additions to unsymmetrically substituted trigonal carbons

5. Methodology to establish 1,2- and 1,3-difunctionality for the synthesis of carbohydrate derivates

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1. Quaternary Ammonium Salts Interact with Enolates and Sulfonates via Formation of Multiple +N-C-H Hydrogen Bonding Interactions;Catalysts;2022-07-21

2. A new method for the synthesis of chalcone derivatives promoted by PPh3/I2under non-alkaline conditions;Synthetic Communications;2020-11-20

3. First enantioselective synthesis of gingesulfonic acids and unequivocal determination of their absolute stereochemistry;Organic & Biomolecular Chemistry;2020

4. Catalyst- and Additive-Free Chemoselective Transfer Hydrogenation of α-Keto Amides to α-Hydroxy Amides by Sodium Formate;European Journal of Organic Chemistry;2019-09-02

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