Strategies for the synthesis of azafenestradienes and azacyclooctatrienes

We have studied possibles access to two new molecular families that are azacyclooctatrienes and [6.4.6.4]azafenestradienes by using a new synthesis methodology : the 8π azaelectrocylization which, for now has never been described to our knowledge. After few synthetic steps initiated by the 4-exo-dig cyclocarbopalladation, we have obtained different key intermediates as azatrienynes and azatetraenes in order to study the feasibility of the azaelectrocyclization. The influence of differents parameters have been studied in particular the temperature, catalytic addition of transition metal and the introduction of an electron-withdrawing group in different position of the azocine skeleton. By this study, we established some useful parameters to continue the understanding of azaelectrocyclization feasibility.

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Source https://theses.hal.science/tel-00764452
Author Siby, Acetou
Maintainer CCSD
Last Updated May 31, 2026, 11:33 (UTC)
Created May 31, 2026, 11:33 (UTC)
Identifier NNT: 2012STRAF013
Language fr
Rights https://about.hal.science/hal-authorisation-v1/
contributor Laboratoire d'Innovation Thérapeutique (LIT) ; Université de Strasbourg (UNISTRA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)
creator Siby, Acetou
date 2012-02-17T00:00:00
harvest_object_id 08a6be40-bda1-494e-9d28-a922599e79cc
harvest_source_id 3374d638-d20b-4672-ba96-a23232d55657
harvest_source_title test moissonnage SELUNE
metadata_modified 2026-03-30T00:00:00
set_spec type:THESE