Enantiopure 2,3-dihydro-4-pyridones as synthetic intermediates: A concise asymmetric synthesis of (+)-allopumiliotoxin 267A

Authors
Comins, DL Huang, SL McArdle, CL Ingalls, CL
Citation
Dl. Comins et al., Enantiopure 2,3-dihydro-4-pyridones as synthetic intermediates: A concise asymmetric synthesis of (+)-allopumiliotoxin 267A, ORG LETT, 3(3), 2001, pp. 469-471
Citations number
18
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
3
Year of publication
2001
Pages
469 - 471
Database
ISI
SICI code
1523-7060(20010208)3:3<469:E2ASIA>2.0.ZU;2-6
Abstract
[GRAPHICS] A concise asymmetric synthesis of (+)-allopumiliotoxin 267A has been accomp lished using an enantiopure dihydropyridone building block, The synthesis i s highly stereoselective and requires 10 steps from readily available mater ial.