Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetate
Тип публикации: Journal Article
Дата публикации: 1983-01-01
scimago Q3
wos Q3
БС2
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
The ester enolate Claisen rearrangement of (E)- and (Z)-2-butenyl 2-hydroxyacetates gave erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids with high diastereoselectivity via silyl ketene acetals, respectively.
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Sato T., Tajima K., Fujisawa T. Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetate // Tetrahedron Letters. 1983. Vol. 24. No. 7. pp. 729-730.
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Sato T., Tajima K., Fujisawa T. Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetate // Tetrahedron Letters. 1983. Vol. 24. No. 7. pp. 729-730.
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TY - JOUR
DO - 10.1016/S0040-4039(00)81510-5
UR - https://doi.org/10.1016/S0040-4039(00)81510-5
TI - Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetate
T2 - Tetrahedron Letters
AU - Sato, Toshio
AU - Tajima, Kazuhisa
AU - Fujisawa, Tamotsu
PY - 1983
DA - 1983/01/01
PB - Elsevier
SP - 729-730
IS - 7
VL - 24
SN - 0040-4039
SN - 1873-3581
ER -
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@article{1983_Sato,
author = {Toshio Sato and Kazuhisa Tajima and Tamotsu Fujisawa},
title = {Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetate},
journal = {Tetrahedron Letters},
year = {1983},
volume = {24},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016/S0040-4039(00)81510-5},
number = {7},
pages = {729--730},
doi = {10.1016/S0040-4039(00)81510-5}
}
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Sato, Toshio, et al. “Diastereoselective synthesis of erythro- and threo-2-hydroxy-3-methyl-4-pentenoic acids by the ester enolate claisen rearrangement of 2-butenyl 2-hydroxyacetate.” Tetrahedron Letters, vol. 24, no. 7, Jan. 1983, pp. 729-730. https://doi.org/10.1016/S0040-4039(00)81510-5.