以异常稳定的环状水合物形式对洛马维亭A中心环系统进行对映选择性合成。 - Suppr

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超能文献

Enantioselective synthesis of the central ring system of lomaiviticin A in the form of an unusually stable cyclic hydrate.

作者信息

Krygowski Evan S, Murphy-Benenato Kerry, Shair Matthew D

机构信息

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA.

出版信息

Angew Chem Int Ed Engl. 2008;47(9):1680-4. doi: 10.1002/anie.200704830.

DOI:10.1002/anie.200704830

PMID:18214870

Abstract

摘要

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相似文献

Enantioselective synthesis of the central ring system of lomaiviticin A in the form of an unusually stable cyclic hydrate.

Angew Chem Int Ed Engl. 2008;47(9):1680-4. doi: 10.1002/anie.200704830.

Synthesis of the fully glycosylated cyclohexenone core of lomaiviticin A.

Org Lett. 2009 Oct 1;11(19):4322-5. doi: 10.1021/ol901710b.

Enantioselective synthesis of the ent-lomaiviticin A bicyclic core.

Org Lett. 2012 Nov 2;14(21):5484-7. doi: 10.1021/ol302567f. Epub 2012 Oct 17.

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Chemistry. 2010 Nov 22;16(44):13058-62. doi: 10.1002/chem.201002157.

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Org Lett. 2013 May 17;15(10):2390-3. doi: 10.1021/ol400832r. Epub 2013 May 9.

Stereocontrolled assembly of the C3/C3' dideoxy core of lomaiviticin A/B and congeners.

Org Lett. 2008 May 15;10(10):1939-41. doi: 10.1021/ol800460a. Epub 2008 Apr 15.

Development of enantioselective synthetic routes to (-)-kinamycin F and (-)-lomaiviticin aglycon.

J Am Chem Soc. 2012 Oct 17;134(41):17262-73. doi: 10.1021/ja307497h. Epub 2012 Oct 3.

Synthesis studies on the lomaiviticin A aglycone core: development of a divergent, two-directional strategy.

J Org Chem. 2013 May 3;78(9):4499-511. doi: 10.1021/jo4005074. Epub 2013 Apr 15.

Stereocontrolled synthesis of model core systems of lomaiviticins A and B.

Angew Chem Int Ed Engl. 2006 Mar 20;45(13):2076-81. doi: 10.1002/anie.200504466.

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Org Lett. 2007 Nov 8;9(23):4857-9. doi: 10.1021/ol702195w. Epub 2007 Oct 20.

引用本文的文献

A Stereoselective Oxidative Dimerization En Route to (-)-Lomaiviticin A.

Org Lett. 2025 Jan 31;27(4):937-941. doi: 10.1021/acs.orglett.4c04098. Epub 2025 Jan 23.

Stereocontrolled Synthesis of the Fully Glycosylated Monomeric Unit of Lomaiviticin A.

J Am Chem Soc. 2022 Sep 7;144(35):16199-16205. doi: 10.1021/jacs.2c07631. Epub 2022 Aug 23.

Synthesis of the bis(cyclohexenone) core of (-)-lomaiviticin A.

Chem Sci. 2020 Jul 9;11(28):7462-7467. doi: 10.1039/d0sc02770g.

Structure Revision of the Lomaiviticins.

J Am Chem Soc. 2021 May 5;143(17):6578-6585. doi: 10.1021/jacs.1c01729. Epub 2021 Apr 26.

Synthesis and Biological Evaluation of (2,2')-Lomaiviticin A.

J Am Chem Soc. 2021 Jan 20;143(2):1126-1132. doi: 10.1021/jacs.0c11960. Epub 2021 Jan 7.

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Beilstein J Org Chem. 2018 May 7;14:1004-1015. doi: 10.3762/bjoc.14.86. eCollection 2018.

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Chem Rev. 2017 Apr 26;117(8):5784-5863. doi: 10.1021/acs.chemrev.6b00621. Epub 2017 Apr 4.

Multigram Synthesis of 1--Acetyl-3--(4-methoxybenzyl)-4--(9-fluorenylmethoxycarbonyl)-4--methyl-L-pyrrolosamine.

Tetrahedron Lett. 2015 Jun 3;56(23):3231-3234. doi: 10.1016/j.tetlet.2014.12.073.

Discovery of the lomaiviticin biosynthetic gene cluster in .

Tetrahedron. 2014 Jul 8;70(27-28):4156-4164. doi: 10.1016/j.tet.2014.03.009.

Oxidative Coupling of Enolates, Enol Silanes and Enamines: Methods and Natural Product Synthesis.

European J Org Chem. 2012 Sep 1;2012(26):4881-4896. doi: 10.1002/ejoc.201200665. Epub 2012 Jul 16.