Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Magali Vuagnoux"'
Autor:
Alexandre Alexakis, Magali Vuagnoux-d'Augustin, David Martin, Stefan Kehrli, Laetitia Palais, Hélène Hénon, Christine Hawner
Publikováno v:
CHIMIA, Vol 62, Iss 6 (2008)
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition: the formation of all-carbon quaternary centers by reaction with Michael acceptors bearing a polysubstituted unsaturation. Only copper catalysts allow
Externí odkaz:
https://doaj.org/article/0447e38e95ff47eca0a6351b8f63819f
Publikováno v:
Chemistry – A European Journal. 17:6214-6220
In the search for a new access to thujopsanone related compounds by cycloisomerization reactions of unsaturated propargylic alcohols and acetates, we found several interesting reaction types and demonstrated the complementarity of Au, Pt, and Cu cata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4316441b7c982983b106ab1d3234b80f
https://doi.org/10.1002/chem.201002797
https://doi.org/10.1002/chem.201002797
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(4)
(E)-Trisubstituted allylic alcohols are commonly prepared from the corresponding (E)-enals, themselves readily accessible by a simple aldol condensation reaction. We demonstrate that these very same (E)-enals can be converted into (Z)-trisubstituted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fce7294803be4594f5ac79f3e3da656
https://pubmed.ncbi.nlm.nih.gov/21243692
https://pubmed.ncbi.nlm.nih.gov/21243692
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 17(14)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b16073553b9d85a54063a2d86aefe3b8
https://pubmed.ncbi.nlm.nih.gov/21381139
https://pubmed.ncbi.nlm.nih.gov/21381139
Publikováno v:
Angewandte Chemie (International ed. in English). 48(39)
We report herein the first enantioselective, direct synthesis of the highly prized natural sandalwood odorant ( )-b-santalol (( )-1). The key step in the synthesis is an efficient copper-catalyzed rearrangement of an enynol. The increasing scarcity o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d42663a72de89a9247e7985c211d1fe
https://pubmed.ncbi.nlm.nih.gov/19705395
https://pubmed.ncbi.nlm.nih.gov/19705395
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.