Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Methoxyacetaldehyde"'
Autor:
Santiago Mata, Elena R. Alonso, Lucie Kolesniková, JoséL. Alonso, Belén Tercero, Isabel Peña, José Cernicharo
Context. Methoxyacetaldehyde belongs to a group of structural isomers with the general formula C3H6O2, of which methyl acetate and ethyl formate are known interstellar molecules. Rotational data available for methoxyacetaldehyde are limited to 40 GHz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::054a2c7742d2ab2cd04ce62c72a25e5e
https://europepmc.org/articles/PMC6290985/
https://europepmc.org/articles/PMC6290985/
Autor:
Christopher D. McCune, Jacob A. Friest, Sandeep K. Ginotra, David B. Berkowitz, Matthew L. Beio
Publikováno v:
Tetrahedron Letters. 56:3575-3579
Described are the synthesis and application of α-t-butyldimethylsilyl-α-methoxyacetaldehyde as a formal methoxyvinyl cation equivalent. Addition of Grignard reagents to the title aldehyde, followed by treatment of the intermediate β-hydroxysilanes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::725cbccec781dcd6a0fa0a9cb98c3b71
https://doi.org/10.1016/j.tetlet.2015.02.122
https://doi.org/10.1016/j.tetlet.2015.02.122
Autor:
Jacob A. Friest, Sandeep K. Ginotra, Matthew L. Beio, David B. Berkowitz, Christopher D. McCune
Publikováno v:
ChemInform. 46
Described are the synthesis and application of α-t-butyldimethylsilyl-α-methoxyacetaldehyde as a formal methoxyvinyl cation equivalent. Addition of Grignard reagents to the title aldehyde, followed by treatment of the intermediate β-hydroxysilanes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa32fbf5ed3b95c8dd0164b34ce6a1b8
https://doi.org/10.1002/chin.201539040
https://doi.org/10.1002/chin.201539040
Autor:
Akira Yoshida, Toshihiro Kawamoto, Keiichi I. Nakayama, Naoki Kunugita, Keiko Nakayama, Tadasuke Tsukiyama, Kyoko Kitagawa, Kohji Okamoto
Publikováno v:
FEBS Letters. 476:306-311
A principal pathway of 2-methoxyethanol (ME) metabolism is to the toxic oxidative product, methoxyacetaldehyde (MALD). To assess the role of aldehyde dehydrogenase (ALDH) in MALD metabolism, in vitro MALD oxidation was examined with liver subcellular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::123830ff08291c69cc57f78688fc21a5
https://doi.org/10.1016/s0014-5793(00)01710-5
https://doi.org/10.1016/s0014-5793(00)01710-5
Akademický článek
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Autor:
Laurent Gate, J. Paul, Paule Vasseur, O. Poirot, Nicole Pages, Haim Tapiero, C. Rast, S. Dhalluin, Z. Elias, G Nguyen-Ba
Publikováno v:
Toxicology Letters. 95:109
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::527a3a191931fcdb27bb71a2a0463315
https://doi.org/10.1016/s0378-4274(98)80430-x
https://doi.org/10.1016/s0378-4274(98)80430-x
Akademický článek
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Autor:
Carl N. Skold
Publikováno v:
Synthetic Communications. 6:119-124
In our work on the synthesis of cephalotaxine, we wished to prepare the α-methoxy-αβ-unsaturated aldehyde 2. Since aldehyde 1 was available2, we needed to find an efficient method for carrying what is effectively an aldol condensation between alde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bffd13c0c090f8f3c7824e4a8d1c11e2
https://doi.org/10.1080/00397917608072620
https://doi.org/10.1080/00397917608072620
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 11:657-662
1. Methods for the synthesis of dimethoxyethylene were worked out. 2. Dimethoxyethylene, like other vinyl ethers, condenses with alcohols including ethylene glycol, with orthoformic ester, with acetals, and with carbon tetrachloride. 3. Methoxyacetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72b039544299572afa83cda462fb2017
https://doi.org/10.1007/bf00904771
https://doi.org/10.1007/bf00904771
Publikováno v:
Journal of the American Chemical Society. 91:3577-3582
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0b8bae81a11dbbb7481a4efd2367518
https://doi.org/10.1021/ja01041a024
https://doi.org/10.1021/ja01041a024