Asymmetric total synthesis of (+)-phomalactone, (+)-acetylphomalactone and (+)-asperlin utilizing a novel syn-selective C4-oxa-vinylogous urethane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Absolute Configurations of Asperlin, a Metabolite ofAspergillus nidulans, and Its Related Compounds
2. Nonracemic Syn-Selective Aldol Reactions with a Second-Generation Vinylogous Urethane Lithium Enolate
3. Large scale preparation of versatile chiral auxiliaries derived from (S)-proline1
4. Asymmetric Syn-Selective Aldol Reactions of γ-Oxygenated Vinylogous Urethane with a Second Generation Chiral Auxiliary: Application in Construction of (+)-3-Deoxy-d-manno-2-octulosonic Acid
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1. Total Synthesis of 5-Hydroxygoniothalamin;Synthesis;2018-10-01
2. Stereoselective Synthesis of C1-C7 and C6-C22 Fragments of Phostriecin, Goniothalamines, and Their Analogues;European Journal of Organic Chemistry;2018-08-13
3. anti-Selective aldol reactions of chiral alcohol substituted γ-benzyloxyl vinylogous urethanes and the synthesis of 3-benzyloxyl-4-hydroxylalkan-2-ones;Tetrahedron: Asymmetry;2017-11
4. Phomalactone from a Phytopathogenic Fungus Infecting ZINNIA elegans (ASTERACEAE) Leaves;Journal of Chemical Ecology;2015-07
5. Phomalactone optimization and production of entomopathogenic fungi byOphiocordyceps communisBCC 1842 and BCC 2763;Preparative Biochemistry and Biotechnology;2014-10-06
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