stagonolide and pyrenophorol

stagonolide has been researched along with pyrenophorol* in 1 studies

*pyrenophorol: isolated from a Drechslera avena; structure in first source [MeSH]

Other Studies

1 other study(ies) available for stagonolide and pyrenophorol

Article	Year
A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: application to asymmetric synthesis of decarestrictine L, pyrenophorol, and stagonolide E. The Journal of organic chemistry, 2014, Sep-05, Volume: 79, Issue:17 The stereomers of hept-6-ene-2,5-diol derivatives were conceived as useful chiral intermediates and were synthesized starting from sulcatol using two lipase-catalyzed acylation reactions as the key steps. The versatility of the intermediates was demonstrated by converting them to the titled tetrahydropyran, macrolide, and macrodiolide compounds using standard synthetic protocols. Topics: Acylation; Catalysis; Heterocyclic Compounds; Heterocyclic Compounds, 1-Ring; Ketones; Lactones; Lipase; Macrolides; Molecular Structure; Pyrans; Stereoisomerism	2014

Article

Year

A chemoenzymatic synthesis of hept-6-ene-2,5-diol stereomers: application to asymmetric synthesis of decarestrictine L, pyrenophorol, and stagonolide E.

The Journal of organic chemistry, 2014, Sep-05, Volume: 79, Issue:17

The stereomers of hept-6-ene-2,5-diol derivatives were conceived as useful chiral intermediates and were synthesized starting from sulcatol using two lipase-catalyzed acylation reactions as the key steps. The versatility of the intermediates was demonstrated by converting them to the titled tetrahydropyran, macrolide, and macrodiolide compounds using standard synthetic protocols.

Topics: Acylation; Catalysis; Heterocyclic Compounds; Heterocyclic Compounds, 1-Ring; Ketones; Lactones; Lipase; Macrolides; Molecular Structure; Pyrans; Stereoisomerism

2014