The synthesis of C2 symmetry diesters of (3R,4R)-TTFOL through a green and stereoselective (2R,3R)-TADDOL rearrangement-Reference-Cited by-同舟云学术

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The synthesis of C2 symmetry diesters of (3R,4R)-TTFOL through a green and stereoselective (2R,3R)-TADDOL rearrangement

Published:2015-12 Issue:23 Volume:26 Page:1341-1347
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Costantino Andrea R.,Montiel Schneider María Gabriela,Galdámez Antonio,Ocampo Romina A.,Mandolesi Sandra D.,Koll Liliana C.

Funder

ANPCyT

CONICET

Universidad Nacional del Sur

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference37 articles.

1. Greenés Protective Group in Organic Synthesis;Wuts,2007

2. Asymmetric Catalysis Special Feature Part I: New biphenol-based, fine-tunable monodentate phosphoramidite ligands for catalytic asymmetric transformations

3. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors

4. Asymmetric Hydroformylation Using Taddol-Based Chiral Phosphine−Phosphite Ligands

5. Privileged Chiral Catalysts

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1. Toward the cholinesterase inhibition potential of TADDOL derivatives: Seminal biological and computational studies;Archiv der Pharmazie;2022-07-27

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