Studies in N-amino-3-aza Cope rearrangements
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Insertion of benzyl isocyanide into a Zr–P bond and rearrangement. Atom-economical synthesis of a phosphaalkene
2. Atom economic synthesis of amides via transition metal catalyzed rearrangement of oxaziridines
3. The Introduction of Substituted Vinyl Groups. V. A Rearrangement Involving the Migration of an Allyl Group in a Three-Carbon System1
4. The Rearrangement of Allyl Groups in Three-carbon Systems. IV. Hydrocarbons
5. Tandem Conjugate Additions and 3-Aza-Cope Rearrangements of Tertiary Allyl Amines and Cyclic α-Vinylamines with Acetylenic Sulfones. Applications to Simple and Iterative Ring Expansions Leading to Medium and Large-Ring Nitrogen Heterocycles
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1. Chlorination of α-Cyanoketones and 1, 3-Dicarbonyl Compounds by Using Trichloroisocyanuric Acid as Chlorine Source;Chinese Journal of Organic Chemistry;2018
2. The most Used Claisen Rearrangements in Organic Synthesis: A Review;Revista Virtual de Química;2017
3. N-heteroatom substitution effect in 3-aza-cope rearrangements;Chemistry Central Journal;2013-05-28
4. Iridium-catalyzed allylic alkylation of monosubstituted allylic acetates with azlactone, and separation of diastereoisomers by sequential aza-Cope rearrangement;Tetrahedron;2011-10
5. Molecular Rearrangements: Part 1. Pericyclic Molecular Rearrangements;Organic Reaction Mechanisms · 2008;2011-08-05
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