id paper:paper_01661280_v635_n1-3_p173_Labadie
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spelling paper:paper_01661280_v635_n1-3_p173_Labadie2023-06-08T15:15:23Z Decomposition mechanism of Birch alkylation products of α-tetralones 1,4 Dienones radicals Decomposition pathways Oxygen addition β-Elimination 1 tetralone derivative oxygen alkylation article Birch reduction chemical reaction decomposition elimination reaction organic chemistry synthesis 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01661280_v635_n1-3_p173_Labadie http://hdl.handle.net/20.500.12110/paper_01661280_v635_n1-3_p173_Labadie
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 1,4 Dienones radicals
Decomposition pathways
Oxygen addition
β-Elimination
1 tetralone derivative
oxygen
alkylation
article
Birch reduction
chemical reaction
decomposition
elimination reaction
organic chemistry
synthesis
spellingShingle 1,4 Dienones radicals
Decomposition pathways
Oxygen addition
β-Elimination
1 tetralone derivative
oxygen
alkylation
article
Birch reduction
chemical reaction
decomposition
elimination reaction
organic chemistry
synthesis
Decomposition mechanism of Birch alkylation products of α-tetralones
topic_facet 1,4 Dienones radicals
Decomposition pathways
Oxygen addition
β-Elimination
1 tetralone derivative
oxygen
alkylation
article
Birch reduction
chemical reaction
decomposition
elimination reaction
organic chemistry
synthesis
title Decomposition mechanism of Birch alkylation products of α-tetralones
title_short Decomposition mechanism of Birch alkylation products of α-tetralones
title_full Decomposition mechanism of Birch alkylation products of α-tetralones
title_fullStr Decomposition mechanism of Birch alkylation products of α-tetralones
title_full_unstemmed Decomposition mechanism of Birch alkylation products of α-tetralones
title_sort decomposition mechanism of birch alkylation products of α-tetralones
publishDate 2003
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01661280_v635_n1-3_p173_Labadie
http://hdl.handle.net/20.500.12110/paper_01661280_v635_n1-3_p173_Labadie
_version_ 1768546535713275904