Total asymmetric synthesis of sperabillins B and DElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b3/b305740b/

Autor: Davies, Stephen G., Kelly, Richard J., Price Mortimer, Anne J.
Zdroj: Chemical Communications; 2003, Vol. 2003 Issue: 17 p2132-2133, 2p
Abstrakt: A consise route to the core fragment of sperabillins B and D, methyl 3R,5R,6R-3,6-diamino-5-hydroxyheptanoate, has been developed with a subsequent novel protection strategy allowing the total asymmetric synthesis of sperabillins B and D.
Databáze: Supplemental Index