id paper:paper_00086215_v341_n18_p2973_RomeroZaliz
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spelling paper:paper_00086215_v341_n18_p2973_RomeroZaliz2023-06-08T14:32:52Z Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester Romero Zaliz, Carmen Lorena Varela, Oscar José ε-Caprolactone Aldono-1,6-lactone Copolyester d-Galactono-1,4-lactone Derivatives Monomers Organic acids Polyesters Polymerization Sugar (sucrose) ε-Caprolactone Aldono-1,6-lactone Copolyesters d-Galactono-1,4-lactone Ketones 2,3,4,6 tetra o methyl dextro galactonic acid dextro galactono 1,4 lactone epsilon caprolactone lactone derivative per o methyl dextro galactono 1,6 lactone polyester scandium triflate trifluoromethanesulfonic acid unclassified drug article deprotection reaction lactonization methylation polymerization priority journal synthesis Hexanoic Acids Lactones Polyesters Sugar Acids Tetra 2,3,4,6-Tetra-O-methyl-d-galactonic acid (5) was readily prepared from d-galactono-1,4-lactone (1) in 47% yield. The sequence involves tritylation of HO-6 of 1, followed by O-permethylation and deprotection. Lactonization of 5 led to the per-O-methyl-d-galactono-1,6-lactone, which was copolymerized with ε-caprolactone by ring-opening polymerization catalyzed by scandium triflate. The incorporation of the sugar comonomer into the polyester chain was about 10%. © 2006 Elsevier Ltd. All rights reserved. Fil:Romero Zaliz, C.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Varela, O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2006 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v341_n18_p2973_RomeroZaliz http://hdl.handle.net/20.500.12110/paper_00086215_v341_n18_p2973_RomeroZaliz
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic ε-Caprolactone
Aldono-1,6-lactone
Copolyester
d-Galactono-1,4-lactone
Derivatives
Monomers
Organic acids
Polyesters
Polymerization
Sugar (sucrose)
ε-Caprolactone
Aldono-1,6-lactone
Copolyesters
d-Galactono-1,4-lactone
Ketones
2,3,4,6 tetra o methyl dextro galactonic acid
dextro galactono 1,4 lactone
epsilon caprolactone
lactone derivative
per o methyl dextro galactono 1,6 lactone
polyester
scandium triflate
trifluoromethanesulfonic acid
unclassified drug
article
deprotection reaction
lactonization
methylation
polymerization
priority journal
synthesis
Hexanoic Acids
Lactones
Polyesters
Sugar Acids
Tetra
spellingShingle ε-Caprolactone
Aldono-1,6-lactone
Copolyester
d-Galactono-1,4-lactone
Derivatives
Monomers
Organic acids
Polyesters
Polymerization
Sugar (sucrose)
ε-Caprolactone
Aldono-1,6-lactone
Copolyesters
d-Galactono-1,4-lactone
Ketones
2,3,4,6 tetra o methyl dextro galactonic acid
dextro galactono 1,4 lactone
epsilon caprolactone
lactone derivative
per o methyl dextro galactono 1,6 lactone
polyester
scandium triflate
trifluoromethanesulfonic acid
unclassified drug
article
deprotection reaction
lactonization
methylation
polymerization
priority journal
synthesis
Hexanoic Acids
Lactones
Polyesters
Sugar Acids
Tetra
Romero Zaliz, Carmen Lorena
Varela, Oscar José
Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
topic_facet ε-Caprolactone
Aldono-1,6-lactone
Copolyester
d-Galactono-1,4-lactone
Derivatives
Monomers
Organic acids
Polyesters
Polymerization
Sugar (sucrose)
ε-Caprolactone
Aldono-1,6-lactone
Copolyesters
d-Galactono-1,4-lactone
Ketones
2,3,4,6 tetra o methyl dextro galactonic acid
dextro galactono 1,4 lactone
epsilon caprolactone
lactone derivative
per o methyl dextro galactono 1,6 lactone
polyester
scandium triflate
trifluoromethanesulfonic acid
unclassified drug
article
deprotection reaction
lactonization
methylation
polymerization
priority journal
synthesis
Hexanoic Acids
Lactones
Polyesters
Sugar Acids
Tetra
description 2,3,4,6-Tetra-O-methyl-d-galactonic acid (5) was readily prepared from d-galactono-1,4-lactone (1) in 47% yield. The sequence involves tritylation of HO-6 of 1, followed by O-permethylation and deprotection. Lactonization of 5 led to the per-O-methyl-d-galactono-1,6-lactone, which was copolymerized with ε-caprolactone by ring-opening polymerization catalyzed by scandium triflate. The incorporation of the sugar comonomer into the polyester chain was about 10%. © 2006 Elsevier Ltd. All rights reserved.
author Romero Zaliz, Carmen Lorena
Varela, Oscar José
author_facet Romero Zaliz, Carmen Lorena
Varela, Oscar José
author_sort Romero Zaliz, Carmen Lorena
title Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
title_short Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
title_full Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
title_fullStr Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
title_full_unstemmed Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
title_sort facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester
publishDate 2006
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v341_n18_p2973_RomeroZaliz
http://hdl.handle.net/20.500.12110/paper_00086215_v341_n18_p2973_RomeroZaliz
work_keys_str_mv AT romerozalizcarmenlorena facilesynthesisofadgalactono16lactonederivativeaprecursorofacopolyester
AT varelaoscarjose facilesynthesisofadgalactono16lactonederivativeaprecursorofacopolyester
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