Lewis acid catalyzed Diels-Alder additions of cyclopentadiene to methyl (E)- and (Z)-(S)-4,5-di-O-isopropylidenepent-2-enoates: Rate and stereoselectivity.

Zhiyu Chen; Rosa M. Ortuño

doi:10.1016/S0957-4166(00)82295-8

Lewis acid catalyzed Diels-Alder additions of cyclopentadiene to methyl (E)- and (Z)-(S)-4,5-di-O-isopropylidenepent-2-enoates: Rate and stereoselectivity.

Zhiyu Chen, Rosa M. Ortuño

Departamento de Química

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

12 Citas (Scopus)

Resumen

Rate, and endo/exo and facial diastereostereoselectivity of the title reactions have been highly enhanced under the action of aluminum, among other metals used as catalysts, compared to the thermal processes. EtAlCl2 and Et2AlCl were the reagents that afforded the best results. © 1992.

Idioma original	Inglés
Páginas (desde-hasta)	621-628
Publicación	Tetrahedron: asymmetry
Volumen	3
N.º	5
DOI	https://doi.org/10.1016/S0957-4166(00)82295-8
Estado	Publicada - 1 ene 1992

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title = "Lewis acid catalyzed Diels-Alder additions of cyclopentadiene to methyl (E)- and (Z)-(S)-4,5-di-O-isopropylidenepent-2-enoates: Rate and stereoselectivity.",

abstract = "Rate, and endo/exo and facial diastereostereoselectivity of the title reactions have been highly enhanced under the action of aluminum, among other metals used as catalysts, compared to the thermal processes. EtAlCl2 and Et2AlCl were the reagents that afforded the best results. {\textcopyright} 1992.",

author = "Zhiyu Chen and Ortu{\~n}o, {Rosa M.}",

year = "1992",

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TY - JOUR

T1 - Lewis acid catalyzed Diels-Alder additions of cyclopentadiene to methyl (E)- and (Z)-(S)-4,5-di-O-isopropylidenepent-2-enoates: Rate and stereoselectivity.

AU - Chen, Zhiyu

AU - Ortuño, Rosa M.

PY - 1992/1/1

Y1 - 1992/1/1

N2 - Rate, and endo/exo and facial diastereostereoselectivity of the title reactions have been highly enhanced under the action of aluminum, among other metals used as catalysts, compared to the thermal processes. EtAlCl2 and Et2AlCl were the reagents that afforded the best results. © 1992.

AB - Rate, and endo/exo and facial diastereostereoselectivity of the title reactions have been highly enhanced under the action of aluminum, among other metals used as catalysts, compared to the thermal processes. EtAlCl2 and Et2AlCl were the reagents that afforded the best results. © 1992.

U2 - 10.1016/S0957-4166(00)82295-8

DO - 10.1016/S0957-4166(00)82295-8

M3 - Article

SN - 0957-4166

VL - 3

SP - 621

EP - 628

JO - Tetrahedron: asymmetry

JF - Tetrahedron: asymmetry

IS - 5

ER -

Lewis acid catalyzed Diels-Alder additions of cyclopentadiene to methyl (E)- and (Z)-(S)-4,5-di-O-isopropylidenepent-2-enoates: Rate and stereoselectivity.

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