New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors
Publication type: Journal Article
Publication date: 2009-12-01
Catalysis
Organic Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
A new synthetic route of to pharmaceutical intermediates (S)-1a–b and (S)-14 is reported. The reaction pathway is based on the baker’s yeast-mediated reduction of the α-alkoxy cinnamaldehydes 9a–c to give the corresponding (S)-alcohols in good yields and excellent ee.
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GOST
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Brenna E. et al. New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors // Tetrahedron Asymmetry. 2009. Vol. 20. No. 23. pp. 2694-2698.
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Brenna E., Fuganti C., Gatti F., Parmeggiani F. New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors // Tetrahedron Asymmetry. 2009. Vol. 20. No. 23. pp. 2694-2698.
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RIS
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TY - JOUR
DO - 10.1016/j.tetasy.2009.10.027
UR - https://doi.org/10.1016/j.tetasy.2009.10.027
TI - New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors
T2 - Tetrahedron Asymmetry
AU - Brenna, Elisabetta
AU - Fuganti, Claudio
AU - Gatti, Francesco
AU - Parmeggiani, Fabio
PY - 2009
DA - 2009/12/01
PB - Elsevier
SP - 2694-2698
IS - 23
VL - 20
SN - 0957-4166
SN - 1362-511X
ER -
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BibTex (up to 50 authors)
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@article{2009_Brenna,
author = {Elisabetta Brenna and Claudio Fuganti and Francesco Gatti and Fabio Parmeggiani},
title = {New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors},
journal = {Tetrahedron Asymmetry},
year = {2009},
volume = {20},
publisher = {Elsevier},
month = {dec},
url = {https://doi.org/10.1016/j.tetasy.2009.10.027},
number = {23},
pages = {2694--2698},
doi = {10.1016/j.tetasy.2009.10.027}
}
Cite this
MLA
Copy
Brenna, Elisabetta, et al. “New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors.” Tetrahedron Asymmetry, vol. 20, no. 23, Dec. 2009, pp. 2694-2698. https://doi.org/10.1016/j.tetasy.2009.10.027.