Stereoselective 1,5-rearrangement of vinylketene-N,O-acetals: novel vinylogous Ferrier reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. 1,3-Rearrangement of ketene-N,O-acetals
2. The conversion of carbohydrate derivatives into functionalized cyclohexanes and cyclopentanes
3. Novel stereoselective construction of a quaternary carbon: application to synthesis of the cyclopentenedione moiety of madindolines
4. Total Synthesis of Madindoline A.
5. Stereoselective construction of a quaternary carbon substituted with multifunctional groups: application to the concise synthesis of (+)-ethosuximide
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1. A new synthesis of highly functionalized cyclohexenes via a vinylogous Ferrier-Petasis cyclization reaction;Tetrahedron;2017-12
2. Concise Synthesis of 6-Formylindolo[3,2-b]carbazole (FICZ);Chemistry Letters;2014-12-05
3. 1,4-Elimination/Brønsted acid catalyzed aza-Ferrier reaction sequence as an entry to β-amino-β,γ-unsaturated aldehydes;Tetrahedron;2013-04
4. Ferrier Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
5. Development of Enolate Chemistry and Total Syntheses of Bioact ive Natural Products;Journal of Synthetic Organic Chemistry, Japan;2009
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