Log in to save to my catalogue

Synthesis of constrained analogues of tryptophan

Synthesis of constrained analogues of tryptophan

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_96180fb139e64b1b945945cd2c94b49b

Synthesis of constrained analogues of tryptophan

About this item

Full title

Synthesis of constrained analogues of tryptophan

Publisher

Germany: Beilstein-Institut

Journal title

Beilstein journal of organic chemistry, 2015-10, Vol.11 (1), p.1997-2006

Language

English

Formats

Publication information

Publisher

Germany: Beilstein-Institut

More information

Scope and Contents

Contents

A Lewis acid-catalysed diastereoselective [4 + 2] cycloaddition of vinylindoles and methyl 2-acetamidoacrylate, leading to methyl 3-acetamido-1,2,3,4-tetrahydrocarbazole-3-carboxylate derivatives, is described. Treatment of the obtained cycloadducts under hydrolytic conditions results in the preparation of a small library of compounds bearing the f...

Alternative Titles

Full title

Synthesis of constrained analogues of tryptophan

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_96180fb139e64b1b945945cd2c94b49b

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_96180fb139e64b1b945945cd2c94b49b

Other Identifiers

ISSN

1860-5397

E-ISSN

1860-5397

DOI

10.3762/bjoc.11.216

How to access this item