Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jörg Erdsack"'
Autor:
Jörg Erdsack, Norbert Krause
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1936-1942 (2013)
The synthesis of (αS,2R)-(2,5-dihydro-1H-pyrrol-2-yl)glycine (22, normethylazafuranomycin) by the gold-catalyzed cycloisomerization of α-aminoallene 17 is described. The target molecule was synthesized in 13 linear steps from Cbz-protected Garner a
Externí odkaz:
https://doaj.org/article/1a7cdc144aa2450eb3a36f4fdabe9536
Autor:
Carl Deutsch, Viola Breker, Hong-Tao Fan, Norbert Krause, Jörg Erdsack, Frank Volz, Yuka Sawama, Yoshinari Sawama, Tao Sun, Christian Winter, Birgit Gockel, Manojkumar Poonoth, Stefan R. K. Minkler, Özge Aksin-Artok, Martta Asikainen
Publikováno v:
Journal of Organometallic Chemistry. 704:1-8
The use of the coinage metals copper, silver, and gold enables an efficient and stereoselective assembly of bioactive heterocycles via allenic intermediates. Whereas copper is mediating or catalyzing the synthesis of functionalized allenes by SN2′-
Autor:
Hong-Tao Fan, Carl Deutsch, Nobuyoshi Morita, Birgit Gockel, Anja Hoffmann-Röder, Jörg Erdsack, Volker Belting, Norbert Krause, Frank Volz
Publikováno v:
Pure and Applied Chemistry. 80:1063-1069
The gold-catalyzed endo-cycloisomerization of allenes bearing nucleophilic substituents in the α- or β-position opens up a versatile access to various five- and six-membered heterocycles. Key features of these transformations are the high reactivit
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 63:o664-o665
The title compound, C20H27NO4, is a synthetic intermediate towards the preparation of novel furanomycin derivatives. Its structure is consistent with the assumed anti selectivity of the allenylation step. Comment The title compound, (I), is a synthet
Publikováno v:
Acta Crystallographica Section E: Structure Reports
The chiral title compound, C(22)H(35)NO(5)SSi, is a precursor of novel furan-omycin derivatives. It crystallizes with two molecules in the asymmetric unit; these show different conformations of the silyl substitutent, as indicated by the Si-O-C-C tor
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 63:o3372-o3372
The title compound, C12H15ClF3NO4, is a side product in a synthesis of novel furanomycin derivatives. The stereochemistry at the bicyclic core is consistent with a halolactonization step. However, racemization also occurred via an unknown mechanism
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 63:o3371-o3371
The chiral title compound, C17H20ClNO5, arose as a side product during the synthesis of novel furanomycin derivatives. The stereochemistry at the bicyclic core is consistent with a halolactonization step. The five-membered rings are nearly perpendi
Autor:
Norbert Krause, Volker Belting, Carl Deutsch, Jörg Erdsack, Hong-Tao Fan, Birgit Gockel, Anja Hoffmann-Röder, Nobuyoshi Morita, Frank Volz
Publikováno v:
Pure & Applied Chemistry; May2008, Vol. 80 Issue 5, p1063-1069, 7p