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Synfacts 2007(7): 0679-0679
DOI: 10.1055/s-2007-968608
DOI: 10.1055/s-2007-968608
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart · New York
Formal Synthesis of (+)-Estrone
D. Soorukram, P. Knochel*
Ludwig-Maximilians Universität München, Germany
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
22. Juni 2007 (online)

Significance
The synthesis of estrone has been a right of passage for many of the great and good in organic chemistry for more than 50 years. In this latest formal synthesis by Soorukram and Knochel, a novel copper(I)-mediated anti-SN2′ allylic substitution reaction developed in the Knochel laboratory was used to generate the sole quaternary stereogenic center in G.