Log in to save to my catalogue

Highly regio- and enantioselective synthesis of chiral polysubstituted 2H-pyrroles

Highly regio- and enantioselective synthesis of chiral polysubstituted 2H-pyrroles

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2918620758

Highly regio- and enantioselective synthesis of chiral polysubstituted 2H-pyrroles

About this item

Full title

Highly regio- and enantioselective synthesis of chiral polysubstituted 2H-pyrroles

Author / Creator

Publisher

Heidelberg: Science China Press

Journal title

Science China. Chemistry, 2014-08, Vol.57 (8), p.1058-1058

Language

English

Formats

Publication information

Publisher

Heidelberg: Science China Press

More information

Scope and Contents

Contents

As one of the most important five-member heterocyclic aromatic rings, pyrrole is widely distributed in numerous natural products and pharmaceutical agents. Asymmetric dearomatization of pyrroles is very attractive in organic synthesis given the fact that highly functionalized chira pyrrolines and pyrrolidines could be easily accessed from the readi...

Alternative Titles

Full title

Highly regio- and enantioselective synthesis of chiral polysubstituted 2H-pyrroles

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2918620758

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2918620758

Other Identifiers

ISSN

1674-7291

E-ISSN

1869-1870

DOI

10.1007/s11426-014-5160-5

How to access this item