Azapropellanes: new fused tetra-azatriazolo[n.3.3.01,x]-dodecenes and tridecenes. Substituted 3,3a,4,5,6,6a-hexahydropyrrolo[2,3-d]-1,2,3-triazoles from a general tandem cycloaddition–rearrangement reaction of 1,2,3-triazolium imides with substituted alkenes: kinetics and mechanism: azolium 1,3-dipoles. Part 3-Reference-Cited by-同舟云学术

Azapropellanes: new fused tetra-azatriazolo[n.3.3.01,x]-dodecenes and tridecenes. Substituted 3,3a,4,5,6,6a-hexahydropyrrolo[2,3-d]-1,2,3-triazoles from a general tandem cycloaddition–rearrangement reaction of 1,2,3-triazolium imides with substituted alkenes: kinetics and mechanism: azolium 1,3-dipoles. Part 3

Published:1990 Issue:9 Volume: Page:2537-2544
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Butler Richard N.,Evans Ann M.,Gillan Ann M.,James John P.,McNeela Eithne M.,Cunningham Desmond,McArdle Patrick

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1990/P1/P19900002537

Reference18 articles.

1. Regioselective intramolecular rearrangements in 1,2-bis(areneazo)cycloalkenes via triazolium imide 1,3-dipoles: examples of a new Fischer indole-type rearrangement. Azolium 1,3-dipoles. Part 2

2. Photochemical and thermal transformations of azomethine imines

3. Mesoionic 1-phenylimino-2,4,5-triphenyl-1,2,3-triazole: a new 1,3-dipolar system

4. 1,3-dipolar cycloadditions of anhydro 1-phenylimino-2,4,5-triphenyl-1,2,3-triazolium hydroxide

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