X=Y–ZH system as potential 1,3-dipoles. Part 59: Cascade 1,3-azaprotio cyclotransfer–1,3-dipolar cycloaddition (1,3-APT–1,3-DC) reactions of benzobicyclo[3.3.1]non-5-en-9-one oxime-Reference-Cited by-同舟云学术

X=Y–ZH system as potential 1,3-dipoles. Part 59: Cascade 1,3-azaprotio cyclotransfer–1,3-dipolar cycloaddition (1,3-APT–1,3-DC) reactions of benzobicyclo[3.3.1]non-5-en-9-one oxime

Published:2003-12 Issue:50 Volume:59 Page:9997-10007
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Dondas H.Ali,Fishwick Colin W.G,Grigg Ronald,Thornton-Pett Mark

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Spiro- and bridged-ring forming electrophile induced → oxime → nitrone cycloaddition cascades. Multiplication of chirality

2. X=Y–ZH Systems as potential 1,3-dipoles. Part 52: Fused-ring forming electrophile induced oxime→nitrone→cycloaddition cascades

3. X=Y–ZH Systems as potential 1,3-dipoles. Part 53: Sequential nucleophilic ring opening-1,3-dipolar cycloaddition reactions of Z-oxime anions with aziridines and dipolarophiles

4. Stereoselective electrophile-induced mono- and bis-cyclisation–fragmentation reactions of alkenyl oxime O-allyl and O-benzyl ethers. Synthesis of dihydropinidine

5. X=Y-ZH systems as potential 1,3-dipoles. Part 48. Enantiopure cycloadducts from oxime-nitrone-isoxazolidine cascades

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1. Causation in a Cascade: The Origins of Selectivities in Intramolecular Nitrone Cycloadditions;Journal of the American Chemical Society;2012-07-12

2. Reverse Cope Elimination of Hydroxylamines and Alkenes or Alkynes: Theoretical Investigation of Tether Length and Substituent Effects;Journal of the American Chemical Society;2012-01-17

3. A green chemical approach for the N-alkylation of aldoximes to form nitrones in organized aqueous media and their in situcycloaddition with olefins;Green Chem.;2009

4. Synthesis And Biological Evaluation Of Some New Alicyclicspiro-2'-(1',3'-Oxazolidine) Derivatives;Heterocyclic Communications;2009-01

5. Bicyclic 5-5 Systems: Three Heteroatoms 1:2;Comprehensive Heterocyclic Chemistry III;2008