Palladium-catalyzed rearrangement of α-cyanoallylic acetates application to a new synthetic method for furans
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Palladium(II)-catalyzed exchange and isomerization reactions. III. Allylic esters isomerization in acetic acid catalyzed by palladium(II) chloride
2. Complete transfer of chirality in the [3,3]-sigmatropic rearrangement of allylic acetates catalyzed by palladium(II). Application to stereocontrolled syntheses of prostaglandins possessing either the C-15(S) or C-15(R) configuration
3. A NEW SYNTHETIC METHOD FOR PELLITORINE
4. A NEW SYNTHETIC METHOD FOR PELLITORINE
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1. Palladium(0)‐Catalyzed Rearrangement of Allylic Esters;ChemistrySelect;2020-02-26
2. Tetrakis(triphenylphosphine)palladium(0);Encyclopedia of Reagents for Organic Synthesis;2017-04-11
3. Rhenium-Catalyzed 1,3-Isomerization of Allylic Alcohols: Scope and Chirality Transfer;The Journal of Organic Chemistry;2006-09-01
4. Simple Preparation of New Functionalized Furan Derivatives via Sequential C-C and C-O Bond Formation Mediated by Palladium-Phosphine Catalyst;Synthesis;2006
5. Stereochemistry of intramolecular Diels–Alder furan (IMDAF) reactions of furyl-substituted chiral ethanolamides;Org. Biomol. Chem.;2003
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