Stereodivergent Synthesis of Pseudotabersonine Alkaloids

Published on 2017-09-13T14:33:51Z (GMT) by
An eight-step stereodivergent synthesis of enantiomerically pure (−)-14-epi-pseudo­tabersonine and (+)-pseudotabersonine has been developed from a common <i>N</i>-<i>tert</i>-butane­sulfinyl ketimine key intermediate.

Cite this collection

Kazak, Mihail; Priede, Martins; Shubin, Kirill; Bartrum, Hannah E.; Poisson, Jean-François; Suna, Edgars (2017): Stereodivergent Synthesis of Pseudotabersonine Alkaloids. ACS Publications.

https://doi.org/10.1021/acs.orglett.7b02635

Retrieved: 07:13, Nov 22, 2017 (GMT)