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The Ir(III)-catalyzed synthesis of 3-pyrrolidinols and 4-piperidinols combining 1,2,4-butanetriol or 1,3,5-pentanetriol with primary amines was carried out. This borrowing hydrogen methodology (BH) was further extended to the sequential diamination o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dfa27510a2e8f90ad3552ef9053b4fa
https://doi.org/10.26434/chemrxiv-2023-ctmh2
https://doi.org/10.26434/chemrxiv-2023-ctmh2
Publikováno v:
Organic Letters
Organic Letters, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
Organic Letters, American Chemical Society, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
Organic Letters, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
Organic Letters, American Chemical Society, 2012, 14 (1), pp.58-61. ⟨10.1021/ol202829u⟩
International audience; We report a TMSI-promoted Prins cyclization reaction with ketones as carbonyl partners to prepare polysubstituted chiral spirotetrahydropyrans. In the presence of racemic 2-methylcyclohexanone a dynamic kinetic resolution occu
Autor:
Mickael Jean, Naresh Tumma, Arnaud Bondon, Maiwenn Jacolot, Srivari Chandrasekhar, Pierre van de Weghe
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (14), pp.7169-75. ⟨10.1021/jo401116r⟩
Journal of Organic Chemistry, 2013, 78 (14), pp.7169-75. ⟨10.1021/jo401116r⟩
Journal of Organic Chemistry, American Chemical Society, 2013, 78 (14), pp.7169-75. ⟨10.1021/jo401116r⟩
Journal of Organic Chemistry, 2013, 78 (14), pp.7169-75. ⟨10.1021/jo401116r⟩
International audience; We disclose the first total synthesis of stachybotrin C, a potent neuroprotective natural compound. All of the four stereoisomers have been prepared and fully characterized with the aim to attribute the absolute configuration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcfa84adcf70ba7ea1d819ed4bf7b9ee
https://hal-univ-rennes1.archives-ouvertes.fr/hal-00862776
https://hal-univ-rennes1.archives-ouvertes.fr/hal-00862776
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2012, 23 (20), pp.2919-2922. ⟨10.1055/s-0032-1317528⟩
SYNLETT, 2012, 23 (20), pp.2919-2922. ⟨10.1055/s-0032-1317528⟩
SYNLETT, Georg Thieme Verlag, 2012, 23 (20), pp.2919-2922. ⟨10.1055/s-0032-1317528⟩
SYNLETT, 2012, 23 (20), pp.2919-2922. ⟨10.1055/s-0032-1317528⟩
International audience; The preparation of racemic des-hydroxy stachybotrin C is described. Different approaches have been studied. Observations made in the course of the synthesis show the efficiency of the intermolecular cyclization between the die
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27bb59379da856d8370adbd32ce02572
https://hal.archives-ouvertes.fr/hal-00841803
https://hal.archives-ouvertes.fr/hal-00841803
Publikováno v:
Organic Letters; Jan2012, Vol. 14 Issue 1, p58-61, 4p