1
ChemInform 2011, 42, issue 09 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Aziridine derivatives R 0040 DOI: 10.1002/chin.201109100 Metalated Aziridines for Cross-Coupling with Aryl and Alkenyl Halides via Pal- ladium Catalysis. — The scope concerning the Negishi coupling of stannylated aziri- dine (I) with alkenyl and aryl halides is examined. The products are formed with reten- tion of stereochemistry and the utility of the process is demonstrated by conversion of product (IIId) into furanomycin and analogues. — (NELSON, J. M.; VEDEJS*, E.; Org. Lett. 12 (2010) 22, 5085-5087, http://dx.doi.org/10.1021/ol101904a ; Dep. Chem., Univ. Mich., Ann Arbor, MI 48109, USA; Eng.) — Mais 09- 100

ChemInform Abstract: Metalated Aziridines for Cross-Coupling with Aryl and Alkenyl Halides via Palladium Catalysis

Embed Size (px)

Citation preview

Page 1: ChemInform Abstract: Metalated Aziridines for Cross-Coupling with Aryl and Alkenyl Halides via Palladium Catalysis

Aziridine derivativesR 0040 DOI: 10.1002/chin.201109100

Metalated Aziridines for Cross-Coupling with Aryl and Alkenyl Halides via Pal-ladium Catalysis. — The scope concerning the Negishi coupling of stannylated aziri-dine (I) with alkenyl and aryl halides is examined. The products are formed with reten-tion of stereochemistry and the utility of the process is demonstrated by conversion of product (IIId) into furanomycin and analogues. — (NELSON, J. M.; VEDEJS*, E.; Org. Lett. 12 (2010) 22, 5085-5087, http://dx.doi.org/10.1021/ol101904a ; Dep. Chem., Univ. Mich., Ann Arbor, MI 48109, USA; Eng.) — Mais

09- 100

ChemInform 2011, 42, issue 09 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim