Journal of the American Chemical Society, volume 139, issue 39, pages 13882-13896
A Unifying Synthesis Approach to the C18-, C19-, and C20-Diterpenoid Alkaloids
Kevin G M Kou
1
,
Svitlana Kulyk
1
,
Christopher J Marth
1
,
Jack C. Lee
1
,
Nicolle A Doering
1
,
Beryl X Li
1
,
Gary M Gallego
1
,
Terry P. Lebold
1
,
Richmond Sarpong
1
Publication type: Journal Article
Publication date: 2017-09-20
scimago Q1
wos Q1
SJR: 5.489
CiteScore: 24.4
Impact factor: 14.4
ISSN: 00027863, 15205126
PubMed ID:
28858498
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Abstract
The secondary metabolites that comprise the diterpenoid alkaloids are categorized into C18, C19, and C20 families depending on the number of contiguous carbon atoms that constitute their central framework. Herein, we detail our efforts to prepare these molecules by chemical synthesis, including a photochemical approach, and ultimately a bioinspired strategy that has resulted in the development of a unifying synthesis of one C18 (weisaconitine D), one C19 (liljestrandinine), and three C20 (cochlearenine, paniculamine, and N-ethyl-1α-hydroxy-17-veratroyldictyzine) natural products from a common intermediate.
Found
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.