Formal synthesis of (+)-lactacystin from l-serine†
Abstract
A formal, stereocontrolled synthesis of lactacystin has been completed from t-Bu-O-L-serine, providing the key intermediate 13, also useful for the generation of a range of C-9 analogues.
We are excited to let you know that our journals content will be migrating to the Silverchair platform, with a planned launch in summer 2026.
All of our content will still be hosted at pubs.rsc.org and the new platform will provide a more intuitive reading and navigation experience, along with improved discovery and indexing of your work.
Details on the move can be found in our partnership announcement.
*a
Ross L.
Goodyear,a
Yohan
Chan,a
Alexandra M. Z.
Slawin
b
and
Steven M.
Allin
c
* Corresponding authors
a
School of Chemistry, University of East Anglia, Norwich Research Park, Norwich, Norfolk NR4 7TJ, UK
E-mail:
p.page@uea.ac.uk
b School of Chemistry, University of St Andrews, St Andrews, Scotland KY16 9ST, UK
c School of Science & Technology, Nottingham Trent University, Clifton, Nottingham NG11 8NS, UK
A formal, stereocontrolled synthesis of lactacystin has been completed from t-Bu-O-L-serine, providing the key intermediate 13, also useful for the generation of a range of C-9 analogues.
Please wait while we load your content...
Something went wrong. Try again?
P. C. Bulman Page, R. L. Goodyear, Y. Chan, A. M. Z. Slawin and S. M. Allin, RSC Adv., 2019, 9, 30019 DOI: 10.1039/C9RA07244F
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.
Fetching data from CrossRef.
This may take some time to load.
Loading related content