Preparation of optically active (R)- and (S)-allene-1,3-dicarboxylates and their asymmetric cycloaddition reactions with cyclopentadiene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Asymmetric diels-alder reaction of a chiral allenic ester : enantioselective synthesis of (−)-β-santalene
2. Periselective intramolecular cycloaddition of allene-1,3-dicarboxylates. Unusual structural feature of [2 + 2] cycloadducts
3. Inter- and intra-molecular reactions of allene-1,3-dicarboxylic acid esters with 2-vinylfurans and 2-vinylthiophenes. A potential route to a BC ring precursor of the nagilactones
4. Asymmetric diels-alder reaction. Cooperative blocking effect in organic synthesis
5. The Absolute Configuration of Pentadiendioic Acid
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1. Cycloadditions II;Key Chiral Auxiliary Applications;2014
2. Thermal Cyclization of Phenylallenes That Containortho-1,3-Dioxolan-2-yl Groups: New Cascade Reactions Initiated by 1,5-Hydride Shifts of Acetalic H Atoms;Chemistry - A European Journal;2013-10-07
3. ChemInform Abstract: Preparation of Optically Active (R)- and (S)-Allene-1,3-dicarboxylates and Their Asymmetric Cycloaddition Reactions with Cyclopentadiene.;ChemInform;2010-08-20
4. Total syntheses of trikentrins and of herbindoles;Tetrahedron;2010-05
5. Diastereoselective Diels−Alder Reactions with an Allenyl-Containing Spiro-Amido Chiral Auxiliary;The Journal of Organic Chemistry;2010-01-05
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