Zobrazeno 1 - 10
of 182
pro vyhledávání: '"Stefan F. Kirsch"'
Autor:
Michael Tapera, Federica Borghi, Jan Lukas Mayer-Figge, Fabia Mittendorf, Ibrahim-Ethem Celik, Adrián Gómez-Suárez, Stefan F. Kirsch
Publikováno v:
Molecules, Vol 29, Iss 15, p 3710 (2024)
Herein, we report a concise and efficient formal synthesis of (+)-hannokinol. Key to this new strategy is the use of a chiral Horner–Wittig reagent, readily available from 2-deoxy-D-ribose, to introduce the chiral 1,3-diol motif.
Externí odkaz:
https://doaj.org/article/bb1dccd0ed3240f6aef22f9723bc06af
Publikováno v:
Tetrahedron Chem, Vol 9, Iss , Pp 100065- (2024)
The macrolide bastimolide A represents an attractive synthetic target due to its promising activity against resistant strains of the malaria pathogen plasmodium falciparum. We report a straightforward formal synthesis of bastimolide A using a Horner-
Externí odkaz:
https://doaj.org/article/cbf8505d37a843c5a4821e817fef56a6
Autor:
Andreas P. Häring, Stefan F. Kirsch
Publikováno v:
Molecules, Vol 20, Iss 11, Pp 20042-20062 (2015)
This review recapitulates all available literature dealing with the synthesis and reactivity of geminal organic di- and triazides. These compound classes are, to a large extent, unexplored despite their promising chemical properties and their simple
Externí odkaz:
https://doaj.org/article/0fd1b1f5d9d64de897ad513bd2a31a5f
Autor:
Sara Hummel, Stefan F. Kirsch
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 847-859 (2011)
Gold catalysis has emerged as one of the most dynamic fields in organic synthesis. Only recently, more and more domino processes, for which gold pre-catalysts were found to be outstandingly effective, were paralleled by employing iodine electrophiles
Externí odkaz:
https://doaj.org/article/99fc64ffa4554f209ab77dfe1f438d8b
Publikováno v:
The Journal of Organic Chemistry. 87:14899-14908
The modular synthesis of 1,3-polyols using a chiral phosphine oxide building block is reported. This versatile building block works in a repetitive way for the stereocontrolled synthesis of a tetraol key intermediate, which serves for the first total
Autor:
Stefan F. Kirsch, Kathrin Bensberg
Publikováno v:
Synthesis. 54:4447-4460
Geminal diazides are uncommon yet powerful tools in organic synthesis. The chemistry of this class of functional compounds is characterized by quite unusual reactivities, including fragmentations and degradations, along with known reactions of organi
Publikováno v:
European Journal of Organic Chemistry. 26
Publikováno v:
Organic & Biomolecular Chemistry.
The first de novo synthesis of (−)- and (+)-aureosurfactin, using a chiral Horner–Wittig building block. Both enantiomers of the biosurfactant are easily accessible starting from only one chiral pool via a bidirectional synthetic strategy.
Autor:
Frederic Ballaschk, Stefan F. Kirsch
Publikováno v:
Iodine Catalysis in Organic Synthesis. :299-334
Publikováno v:
European Journal of Organic Chemistry. 2022