Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marie Claude Roux-Schmitt"'
Autor:
Jacques Corset, Francoise Froment, Marie France Lautie, Nicole Ratovelomanana, Jacqueline Seyden-Penne, Tekla Strzalko, Marie Claude Roux-Schmitt
Publikováno v:
Journal of the American Chemical Society. 115:1684-1694
The structures of Li and K methyl and tert-butyl phenylacetate enolates A,M and B,M have been examined by IR and 13 C NMR spectroscopy in different solvents and solvent mixtures. In the IR, coupling of aromatic ring mode with the v(C . - . O) stretch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18d82deb5529469fe1dd62d3546eb3da
https://doi.org/10.1021/ja00058a012
https://doi.org/10.1021/ja00058a012
Publikováno v:
Tetrahedron. 39:3415-3418
The stereochemistry of trapping of enolates, resulting from reaction of lithiated arylacetonitriles to cyclenones, by methyl iodide, is examined. In a medium such as THF-HMPT , the trans 2,3-disubstituted cyclanones are obtained with good yields, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::954e03577055a0011a80961f39d79140
https://doi.org/10.1016/s0040-4020(01)91594-7
https://doi.org/10.1016/s0040-4020(01)91594-7
Publikováno v:
Synthetic Communications. 11:85-94
The reaction of organolithium derivates with α β unsaturated ketones gives, generally, allylic alcohols resulting from 1–2 addition (1). Recently, it has been shown that 1–4 addition products can be obtained in diethyl ether or in tetrahydrofur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49a89d3e54a120b349e063644f34dc3b
https://doi.org/10.1080/00397918108064287
https://doi.org/10.1080/00397918108064287
Publikováno v:
Tetrahedron Letters. 29:1713-1716
The reaction of methyl 4-bromo-4-methylcrotonate 1 with anionic species ∝- to nitriles does not lead to cyclopropanes via a MIRC process. Products originating from a SN′ reaction, 3 and 6 , are predominantly formed from 2a-c , while products resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3023d22abae8c6b809345b9b747480c5
https://doi.org/10.1016/s0040-4039(00)82025-0
https://doi.org/10.1016/s0040-4039(00)82025-0
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a4d198bcc7ce2c666cf2d7f6caa423
https://doi.org/10.1002/chin.198002188
https://doi.org/10.1002/chin.198002188
Autor:
J. Sansoulet, Marie Claude Roux-Schmitt, Jacqueline Seyden-Penne, Tekla Strzalko, Georges Bram, André Loupy
Publikováno v:
ChemInform. 18
Preparation de sulfones par alkylation d'arenesulfinates a l'aide de composes halogenes. Les dithioacetals sont prepares par reaction de benzenethiol avec des composes gem-dihalogenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73f5cf012e82fff67a55b0269845fc6c
https://doi.org/10.1002/chin.198722170
https://doi.org/10.1002/chin.198722170
Publikováno v:
Chemischer Informationsdienst. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e23947abd1c6934c2bd08d71ef12569a
https://doi.org/10.1002/chin.198103106
https://doi.org/10.1002/chin.198103106