2019-02-19T12:07:13Z
2019-02-19T12:07:13Z
2015-09-25
2019-02-19T12:07:14Z
A unified strategy for the synthesis of the cisphlegmarine group of alkaloids is presented, leading to the first synthesis of serratezomine E (1) as well as the putative structure of huperzine N (2). A contrasteric hydrogenation method was developed based on the use of Wilkinson's catalyst, which allowed the facial selectivity of standard hydrogenation to be completely overturned. Calculations were performed to determine the mechanism, and structures for huperzines M and N are reassigned.
Artículo
Versión aceptada
Inglés
Alcaloides; Compostos heterocíclics; Síntesi orgànica; Productes naturals; Alkaloids; Heterocyclic compounds; Organic synthesis; Natural products
American Chemical Society
Versió postprint del document publicat a: https://doi.org/10.1021/acs.orglett.5b02581
Organic Letters, 2015, vol. 17, num. 20, p. 5084-5087
https://doi.org/10.1021/acs.orglett.5b02581
(c) American Chemical Society , 2015