Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Suzuki coupling reaction (intramol"'
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2008, pp.2355-2359. ⟨10.1055/s-2008-1078209⟩
SYNLETT, Georg Thieme Verlag, 2008, pp.2355-2359. ⟨10.1055/s-2008-1078209⟩
A concise total synthesis of arylomycin A2 was accomplished featuring a key intramol. Suzuki-Miyaura reaction for the formation of the 14-membered meta,meta-cyclophane and direct coupling of a fully elaborated peptide side-chain with the macrocyclic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bbf59d4c85538f0889017fa0ab8a12c
https://hal.archives-ouvertes.fr/hal-00337325
https://hal.archives-ouvertes.fr/hal-00337325
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2007, 9 (12), pp.2401-2404. ⟨10.1021/ol070889p⟩
Organic Letters, American Chemical Society, 2007, 9 (12), pp.2401-2404. ⟨10.1021/ol070889p⟩
Palladium-catalyzed intramol. Suzuki-Miyaura reaction of linear tripeptide afforded the 16-membered DEFG ring of complestatin I in good yield with an excellent atropdiastereoselectivity. Acidic treatment of I triggers a stereospecific rearrangement l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0afcaee75886790c655bdfda4cef866
https://pubmed.ncbi.nlm.nih.gov/17497871
https://pubmed.ncbi.nlm.nih.gov/17497871
