Asymmetrische Synthese von Thiadecalinen : Organokatalytische Dominoreaktionen kombiniert mit intramolekularen Michael-Reaktionen

An efficient asymmetric synthesis of highly substituted thiadecalins using organocatalytic domino-reactions and intramolecular Michael-additions is presented. The combination of organocatalytic domino-reactions and intramolecular Michael-reactions leads to the formation of four new bonds and allows the control of six stereogenic centers. Thiadecalins are known for their antimicrobial properties.

Grantor dc:publisher

Publikationsserver der RWTH Aachen University

Year dc:date

2010

Author dc:creator

• Schmid, Bertram

Contributors dc:contributor

• Enders, Dieter

• info:eu-repo/classification/ddc/540
• Organokatalyse
• Michael-Addition
• Asymmetrische Synthese
• Chemie
• organocatalysis
• asymmetric synthesis

Statement dc:rights

• info:eu-repo/semantics/openAccess

Language dc:language

ger

Identifier

https://publications.rwth-aachen.de/search?p=id:%22RWTH-CONV-124423%22

OAI identifier oai:identifier

oai:publications.rwth-aachen.de:62950