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Enantioselective total synthesis of naturally occurring eushearilide and evaluation of its antifunga...

Enantioselective total synthesis of naturally occurring eushearilide and evaluation of its antifunga...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1824225911

Enantioselective total synthesis of naturally occurring eushearilide and evaluation of its antifungal activity

About this item

Full title

Enantioselective total synthesis of naturally occurring eushearilide and evaluation of its antifungal activity

Publisher

London: Nature Publishing Group UK

Journal title

Journal of antibiotics, 2016-09, Vol.69 (9), p.697-701

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

The asymmetric total synthesis of a newly proposed structure of (3
S
,16
E
,20
E
,23
S
)-(+)-eushearilide was achieved primarily through an asymmetric Mukaiyama aldol reaction, Schlosser-modified Wittig reaction and 2-methyl-6-nitrobenzoic anhydride-mediated macrolactonization. Based on detailed spectroscopic analyses, the o...

Alternative Titles

Full title

Enantioselective total synthesis of naturally occurring eushearilide and evaluation of its antifungal activity

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1824225911

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1824225911

Other Identifiers

ISSN

0021-8820

E-ISSN

1881-1469

DOI

10.1038/ja.2015.146

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