Format:
Online-Ressource
ISSN:
1521-3773
Content:
Abstract: Controlling reaction selectivity is an eternal pursuit for chemists working in chemical synthesis. As part of this endeavor, our group has been exploring the possibility of constructing different natural product skeletons from the same simple starting materials by using different catalytic systems. In our previous work, an isoflavanone skeleton was obtained from the annulation of a salicylaldehyde and an alkyne when a gold catalyst was employed. In this paper, it is shown that a coumarin skeleton can be efficiently obtained through an annulation reaction with the same starting materials, that is, terminal alkynes and salicylaldehydes, by simply switching to a rhodium catalyst. A plausible reaction mechanism is proposed for this new annulation based on isotopic substitution experiments.
In:
volume:53
In:
number:50
In:
year:2014
In:
pages:13862-13865
In:
extent:4
In:
Angewandte Chemie / International edition, Weinheim : Wiley-VCH, 1962-, 53, Heft 50 (2014), 13862-13865 (gesamt 4), 1521-3773
Language:
English
DOI:
10.1002/anie.201407589
URN:
urn:nbn:de:101:1-2023010606202678429770
URL:
https://doi.org/10.1002/anie.201407589
URL:
https://nbn-resolving.org/urn:nbn:de:101:1-2023010606202678429770
URL:
https://d-nb.info/1277367655/34
URL:
https://doi.org/10.1002/anie.201407589