Bicyclo[3.2.0]heptane as a Core Structure for Conformational Locking of 1,3-Bis-Pharmacophores, Exemplified by GABA-Reference-Cited by-同舟云学术

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Bicyclo[3.2.0]heptane as a Core Structure for Conformational Locking of 1,3-Bis-Pharmacophores, Exemplified by GABA

Published:2017-02-01 Issue:13 Volume:23 Page:3126-3138
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Vorberg Raffael¹,Trapp Nils¹^ORCID,Carreira Erick M.¹^ORCID,Müller Klaus¹^ORCID

Affiliation:

1. Laboratorium für Organische Chemie; ETH Zürich; Vladimir-Prelog-Weg 3 8093 Zürich Switzerland

Funder

ETH Zurich

F. Hoffmann-La Roche (CH)

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference117 articles.

1. Spongiolactone, an unusual β-lactone diterpene isovalerate based on a new rearranged spongiane skeleton from

2. Salinosporamide A: A Highly Cytotoxic Proteasome Inhibitor from a Novel Microbial Source, a Marine Bacterium of the New Genus Salinospora

3. Vibralactone: A Lipase Inhibitor with an Unusual Fused β-Lactone Produced by Cultures of the Basidiomycete Boreostereum vibrans

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5. A short synthesis of both enantiomers of 2-aminobicyclo[3.2.0]heptane-2,7-dicarboxylic acid;Tetrahedron Letters;2021-03

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