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Asymmetric Synthesis of Spirocyclic 2-Benzopyrans for Positron Emission Tomography of [sigma]1 Recep...

Asymmetric Synthesis of Spirocyclic 2-Benzopyrans for Positron Emission Tomography of [sigma]1 Recep...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1525784530

Asymmetric Synthesis of Spirocyclic 2-Benzopyrans for Positron Emission Tomography of [sigma]1 Receptors in the Brain

About this item

Full title

Asymmetric Synthesis of Spirocyclic 2-Benzopyrans for Positron Emission Tomography of [sigma]1 Receptors in the Brain

Publisher

Basel: MDPI AG

Journal title

Pharmaceuticals (Basel, Switzerland), 2014-01, Vol.7 (1), p.78

Language

English

Formats

Publication information

Publisher

Basel: MDPI AG

More information

Scope and Contents

Contents

Sharpless asymmetric dihydroxylation of styrene derivative 6 afforded chiral triols (R)-7 and (S)-7, which were cyclized with tosyl chloride in the presence of Bu2SnO to provide 2-benzopyrans (R)-4 and (S)-4 with high regioselectivity. The additional hydroxy moiety in the 4-position was exploited for the introduction of various substituents. Willia...

Alternative Titles

Full title

Asymmetric Synthesis of Spirocyclic 2-Benzopyrans for Positron Emission Tomography of [sigma]1 Receptors in the Brain

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_1525784530

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1525784530

Other Identifiers

E-ISSN

1424-8247

DOI

10.3390/ph7010078

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