Issue 2, 2015

One-pot triangular chemoenzymatic cascades for the syntheses of chiral alkaloids from dopamine

Abstract

We describe novel chemoenzymatic routes to (S)-benzylisoquinoline and (S)-tetrahydroprotoberberine alkaloids using the enzymes transaminase (TAm) and norcoclaurine synthase (NCS) in a one-pot, one-substrate ‘triangular’ cascade. Employment of up to two C–C bond forming steps allows for the rapid generation of molecular complexity under mild conditions.

Graphical abstract: One-pot triangular chemoenzymatic cascades for the syntheses of chiral alkaloids from dopamine

Supplementary files

Article information

Article type
Communication
Submitted
25 ное 2014
Accepted
12 дек 2014
First published
18 дек 2014
This article is Open Access
Creative Commons BY license

Green Chem., 2015,17, 852-855

Author version available

One-pot triangular chemoenzymatic cascades for the syntheses of chiral alkaloids from dopamine

B. R. Lichman, E. D. Lamming, T. Pesnot, J. M. Smith, H. C. Hailes and J. M. Ward, Green Chem., 2015, 17, 852 DOI: 10.1039/C4GC02325K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements