Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Marie-Christine Scherrmann"'
Autor:
Elżbieta Wojaczyńska, Franz Steppeler, Dominika Iwan, Marie-Christine Scherrmann, Alberto Marra
Publikováno v:
Molecules, Vol 26, Iss 23, p 7291 (2021)
Organocatalysis is a very useful tool for the asymmetric synthesis of biologically or pharmacologically active compounds because it avoids the use of noxious metals, which are difficult to eliminate from the target products. Moreover, in many cases,
Externí odkaz:
https://doaj.org/article/aabd16ab027f46b89adedf63328cb9d0
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2351-2357 (2016)
Purification by flash chromatography strongly impacts the greenness of a process. Unfortunately, due to the lack of the relevant literature data, very often this impact cannot be assessed thus preventing the comparison of the environmental factors af
Externí odkaz:
https://doaj.org/article/12dd73bc830a4d45951caae7e191fe89
Publikováno v:
Molecules, Vol 23, Iss 3, p 684 (2018)
A simple and efficient methodology for the nucleophilic aromatic substitution of nitrogen-containing fused heterocycles with interesting biological activities has been developed in an environmentally sound manner using polyethylene glycol (PEG-400) a
Externí odkaz:
https://doaj.org/article/c29136940158438a924eaed648c28c9a
Se fondant sur les principes de Chimie Verte, Jacques Augé et Marie-Christine Scherrmann, tous deux de formation Ingénieur, montrent comment les concepts de Chimie Verte peuvent nous conduire à élaborer une chimie innovante avec des objectifs éc
Publikováno v:
Organic Letters. 22:8522-8527
We have established photochemical access to thietane or tetrahydrothiophene compounds from thiobenzophenone derivatives and acrylonitrile, wherein the product selectivity is controlled by a simple adjustment of the reagent concentration in solution.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d433e10a077e55897c94c5d3923b8260
https://doi.org/10.1021/acs.orglett.0c03128
https://doi.org/10.1021/acs.orglett.0c03128
Autor:
Marie-Christine Scherrmann
Publikováno v:
Biphasic Chemistry and The Solvent Case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37f3b76a5ede623bdcf9ef51c648f3e4
https://doi.org/10.1002/9781119695080.ch3
https://doi.org/10.1002/9781119695080.ch3
Autor:
Franz Steppeler, Marie-Christine Scherrmann, Elżbieta Wojaczyńska, Alberto Marra, Dominika Iwan
Publikováno v:
Molecules, Vol 26, Iss 7291, p 7291 (2021)
Molecules
Molecules
Organocatalysis is a very useful tool for the asymmetric synthesis of biologically or pharmacologically active compounds because it avoids the use of noxious metals, which are difficult to eliminate from the target products. Moreover, in many cases,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5054e3e7cc49192fb0633c9023ac7ee7
https://www.mdpi.com/1420-3049/26/23/7291
https://www.mdpi.com/1420-3049/26/23/7291
Publikováno v:
Green Chemistry. 21:1531-1539
We report here the first investigation of the use of eucalyptol as a new solvent for organic transformations. Heterocycles containing oxygen, sulfur and nitrogen were chosen as targets or as starting materials for widely used palladium-catalysed cros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ddfc93d595d091bf6cf8d53bb602ea2
https://doi.org/10.1039/c8gc04016h
https://doi.org/10.1039/c8gc04016h
Autor:
Thao Anh Minh Nguyen, Régis Guillot, Ahmad F Kassir, Florence Charnay-Pouget, David J. Aitken, Marie-Christine Scherrmann, Thomas Boddaert, Sherif Shaban Ragab
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, 2016, 81 (20), pp.9983-9991. ⟨10.1021/acs.joc.6b01795⟩
Journal of Organic Chemistry, 2016, 81 (20), pp.9983-9991. ⟨10.1021/acs.joc.6b01795⟩
A short synthesis of all four stereoisomers of 3-amino-2-oxetanecarboxylic acid (oxetin) is described. The oxetane core is built using a Paternò-Büchi photochemical [2 + 2] cycloaddition; from the key intermediates, complementary resolution protoco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed2e502bd8b621b6e4f787e503ac30f4
https://doi.org/10.1021/acs.joc.6b01795
https://doi.org/10.1021/acs.joc.6b01795