Stereodivergent Synthesis of Pseudotabersonine Alkaloids

Organic Letters 2017
M. Kazak, M. Priede, K. Shubin, H.E. Bartrum, J.-F. Poisson, Edgars Sūna

An eight-step stereodivergent synthesis of enantiomerically pure (-)-14-epi-pseudotabersonine and (+)-pseudotabersonine has been developed from a common N-tert-butanesulfinyl ketimine key intermediate.

DOI
10.1021/acs.orglett.7b02635
Hyperlink
http://pubs.acs.org/doi/10.1021/acs.orglett.7b02635

Kazak, M., Priede, M., Shubin, K., Bartrum, H., Poisson, J., Sūna, E. Stereodivergent Synthesis of Pseudotabersonine Alkaloids. Organic Letters, 2017, Vol.19, Iss.19, pp.5356-5359. ISSN 1523-7060. Available from: doi:10.1021/acs.orglett.7b02635

Publication language
English (en)