Total Synthesis of Amaminol A: 
Establishment of the Absolute
Stereochemistry

T. T. Kumpulainen, Esa; M. P. Koskinen, Ari; Rissanen, Kari

doi:10.1021/ol7022856.s002

ol7022856_si_002.pdf (3.53 MB)

Total Synthesis of Amaminol A: Establishment of the Absolute Stereochemistry

journal contribution

posted on 2007-11-22, 00:00 authored by Esa T. T. Kumpulainen, Ari M. P. Koskinen, Kari Rissanen

The first synthetic route to amaminol A with use of an organocatalytic intramolecular Diels−Alder reaction is reported. The absolute stereochemistry is proven with a crystallographic image of a cyclic carbamate of amaminol A.

History

Usage metrics

Keywords

image intramolecular Establishment organocatalytic Diel stereochemistry Amaminol Absolute StereochemistryThe cyclic carbamate Total Synthesis amaminol

Licence

CC BY-NC 4.0

Exports

RefWorks

BibTeX

Ref. manager

Endnote

DataCite

NLM

DC