Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Olivier Y. Provoost"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 3, Iss 1, p 8 (2007)
A [3 + 3] annelation of enantiomerically pure aziridine 7 provides the functionalised piperidine 8 that can be elaborated to the indolizidine skeleton in only 4 steps with good stereocontrol.
Externí odkaz:
https://doaj.org/article/3b75263d6e57469b805bd6b43306242c
Publikováno v:
Tetrahedron Letters. 47:331-333
A formal synthesis of (±)-perhydrohistrionicotoxin is described that includes a highly diastereoselective modified Sharpless aziridination and a stepwise [3+3] annelation reaction for the stereoselective construction of the key spiropiperidine motif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::057361812d37348bbb03fcf9a465f834
https://doi.org/10.1016/j.tetlet.2005.11.015
https://doi.org/10.1016/j.tetlet.2005.11.015
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 3, Iss 1, p 8 (2007)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A [3 + 3] annelation of enantiomerically pure aziridine 7 provides the functionalised piperidine 8 that can be elaborated to the indolizidine skeleton in only 4 steps with good stereocontrol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90fc7da164fd41bdfb31025feeb65b66
https://doaj.org/article/3b75263d6e57469b805bd6b43306242c
https://doaj.org/article/3b75263d6e57469b805bd6b43306242c
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f882c63423177207c7e126dad16db983
https://doi.org/10.1002/chin.200535258
https://doi.org/10.1002/chin.200535258