Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Leona J. Gross"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2104-2123 (2016)
The direct oxidative cyclization of 1,5-dienes is a valuable synthetic method for the (dia)stereoselective preparation of substituted tetrahydrofurans. Closely related reactions start from 5,6-dihydroxy or 5-hydroxyalkenes to generate similar product
Externí odkaz:
https://doaj.org/article/6306aeb6fb42483faa4b378dd4c8e201
Autor:
Leona J. Gross, Christian B. W. Stark
Publikováno v:
Organic & Biomolecular Chemistry. 15:4282-4285
We here present a highly efficient and high yielding procedure for the preparation of 2-vinyl tetrahydrofurans starting from α-hydroxymethyl tetrahydrofurans. Best results for this dehydration were achieved using Burgess' reagent in dioxane under mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c8d457f9f67ef9b39eb55618c761ed
https://doi.org/10.1039/c7ob00607a
https://doi.org/10.1039/c7ob00607a
Autor:
Manuela Weber, Dieter Lentz, Christian B. W. Stark, Leona J. Gross, Christian Depken, Alexander Breder, Stefan Leisering, Reinhold Zimmer, Mathias Christmann, Iker Riaño
Publikováno v:
Organic letters. 19(6)
An asymmetric synthesis of the C11-homoterpenoid (+)-Greek tobacco lactone is developed starting from readily available (R)-linalool. The synthesis is comprised of four operations and features a diastereoablative epoxidation and an oxidative tetrahyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cee81be158ed8be3a7012a77c68259b3
https://pubmed.ncbi.nlm.nih.gov/28257212
https://pubmed.ncbi.nlm.nih.gov/28257212
Autor:
Daniel J. Asby, Matthew D. Selby, Ali Tavassoli, Bruno Linclau, Leona J. Gross, Florent Peron, Nathan Bartlett
Publikováno v:
Chemistry - A European Journal. 20:3306-3310
Very high diastereoselectivity can be achieved by 1,3-chelation-controlled allylation of aldehydes that possess a non-chelating α-ether substituent, even if the α-position is a quaternary centre and/or a spiro-epoxide. This reaction was used as a k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6aa94167fc77d36c53fe88afbb1252
https://doi.org/10.1002/chem.201304776
https://doi.org/10.1002/chem.201304776
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2104-2123 (2016)
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2104-2123 (2016)
The direct oxidative cyclization of 1,5-dienes is a valuable synthetic method for the (dia)stereoselective preparation of substituted tetrahydrofurans. Closely related reactions start from 5,6-dihydroxy or 5-hydroxyalkenes to generate similar product
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9c128e593154bad4e9cf20c688423b
https://pubmed.ncbi.nlm.nih.gov/27829917
https://pubmed.ncbi.nlm.nih.gov/27829917
Autor:
Ali Tavassoli, Leona J. Gross, Bruno Linclau, Daniel J. Asby, Nathan Bartlett, Florent Peron, Matthew D. Selby
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12e1f5df4e7e40465f959b71059f027d
https://doi.org/10.1002/chin.201436212
https://doi.org/10.1002/chin.201436212