青蛙生物碱（-）-205B的简洁全合成。 - Suppr

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超能文献

Concise total synthesis of the frog alkaloid (-)-205B.

作者信息

Tsukanov Sergey V, Comins Daniel L

机构信息

Department of Chemistry, North Carolina State University, 2620 Yarbrough Drive, Raleigh, NC 27695-8204, USA.

出版信息

Angew Chem Int Ed Engl. 2011 Sep 5;50(37):8626-8. doi: 10.1002/anie.201103596. Epub 2011 Jul 26.

DOI:10.1002/anie.201103596

PMID:21793144

Abstract

摘要

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Concise total synthesis of the frog alkaloid (-)-205B.

作者信息

Tsukanov Sergey V, Comins Daniel L

机构信息

Department of Chemistry, North Carolina State University, 2620 Yarbrough Drive, Raleigh, NC 27695-8204, USA.

出版信息

Angew Chem Int Ed Engl. 2011 Sep 5;50(37):8626-8. doi: 10.1002/anie.201103596. Epub 2011 Jul 26.

DOI:10.1002/anie.201103596

PMID:21793144

Abstract

摘要

相似文献

Concise total synthesis of the frog alkaloid (-)-205B.

Angew Chem Int Ed Engl. 2011 Sep 5;50(37):8626-8. doi: 10.1002/anie.201103596. Epub 2011 Jul 26.

Total synthesis of the neotropical poison-frog alkaloid (-)-205B.

Org Lett. 2005 Jul 21;7(15):3247-50. doi: 10.1021/ol0510264.

A general, convergent strategy for the construction of indolizidine alkaloids: total syntheses of (-)-indolizidine 223AB and alkaloid (-)-205B.

J Org Chem. 2006 Mar 31;71(7):2547-57. doi: 10.1021/jo052314g.

Total synthesis of alkaloid 205B.

J Org Chem. 2014 Oct 3;79(19):9074-85. doi: 10.1021/jo501415r. Epub 2014 Sep 17.

Total syntheses of (+)-fawcettimine and (+)-lycoposerramine-B.

J Org Chem. 2010 May 21;75(10):3420-6. doi: 10.1021/jo100499h.

Total synthesis of (-)-stemoamide.

J Org Chem. 2007 May 25;72(11):4246-9. doi: 10.1021/jo070498o. Epub 2007 Apr 24.

First total synthesis of cassiarin A, a naturally occurring potent antiplasmodial alkaloid.

Org Lett. 2008 May 15;10(10):1921-2. doi: 10.1021/ol8004112. Epub 2008 Apr 16.

Stereoselective synthesis of pyridinones: application to the synthesis of (-)-barrenazines.

Org Lett. 2006 Jul 6;8(14):2985-8. doi: 10.1021/ol0609006.

Total syntheses of (±)-spiroquinazoline, (-)-alantryphenone, (+)-lapatin A, and (-)-quinadoline B.

Angew Chem Int Ed Engl. 2013 Sep 9;52(37):9759-62. doi: 10.1002/anie.201303893. Epub 2013 Jul 19.

Synthesis of the 10-azatricyclo[3.3.2.0(4,8)]decane core of C20-diterpenoid alkaloid racemulsonine via iodine(III) promoted transannular aziridination reaction.

Org Lett. 2013 May 3;15(9):2206-9. doi: 10.1021/ol400755x. Epub 2013 Apr 15.

引用本文的文献

Grignard Reagent Addition to Pyridinium Salts: A Catalytic Approach to Chiral 1,4-Dihydropyridines.

ACS Catal. 2024 Aug 15;14(17):13030-13039. doi: 10.1021/acscatal.4c03520. eCollection 2024 Sep 6.

A C-H functionalization approach to diverse nitrogenous scaffolds through conjugate addition of catalytic allyliron nucleophiles.

Chem Sci. 2024 May 1;15(23):8850-8857. doi: 10.1039/d4sc00655k. eCollection 2024 Jun 12.

Total synthesis of the natural (-)-205B alkaloid and its activity toward α7 nAChRs.

Org Biomol Chem. 2023 Jan 25;21(4):817-822. doi: 10.1039/d2ob01723g.

Characterization of Cyclic N-Acyliminium Ions by Infrared Ion Spectroscopy.

Chemistry. 2022 Feb 16;28(9):e202104078. doi: 10.1002/chem.202104078. Epub 2021 Dec 29.

Enantioselective Catalytic Dearomative Addition of Grignard Reagents to 4-Methoxypyridinium Ions.

ACS Catal. 2021 Jul 16;11(14):8476-8483. doi: 10.1021/acscatal.1c01544. Epub 2021 Jun 28.

Synthesis and Utility of Dihydropyridine Boronic Esters.

Angew Chem Int Ed Engl. 2016 Feb 5;55(6):2205-9. doi: 10.1002/anie.201510027. Epub 2015 Dec 22.

Total synthesis of alkaloid 205B.

J Org Chem. 2014 Oct 3;79(19):9074-85. doi: 10.1021/jo501415r. Epub 2014 Sep 17.

Biomimetic Aerobic C-H Olefination of Cyclic Enaminones at Room Temperature: Development toward the Synthesis of 1,3,5-Trisubstituted Benzenes.

Adv Synth Catal. 2014 Apr 14;356(6):1359-1369. doi: 10.1002/adsc.201300904.

Palladium-catalyzed direct C-H arylation of cyclic enaminones with aryl iodides.

J Org Chem. 2013 Jun 21;78(12):6163-9. doi: 10.1021/jo400830t. Epub 2013 Jun 10.

Synthesis of alkaloid (-)-205B via stereoselective reductive cross-coupling and intramolecular [3+2] cycloaddition.

J Am Chem Soc. 2012 Sep 19;134(37):15237-40. doi: 10.1021/ja306362m. Epub 2012 Sep 7.