Circular dichroism of michellamines: Independent assignment of axial chirality by calculated and experimental CD spectra-Reference-Cited by-同舟云学术

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Circular dichroism of michellamines: Independent assignment of axial chirality by calculated and experimental CD spectra

Published:1994-01 Issue:26 Volume:50 Page:7807-7814
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bringmann Gerhard,Gulden Klaus-Peter,Hallock Yali F.,Manfredi Kirk P.,Cardellina John H.,Boyd Michael R.,Kramer Bernd,Fleischhauer Jörg

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Novel alkaloids from the tropical plant Ancistrocladus abbreviatus inhibit cell killing by HIV-1 and HIV-2

2. ancistrobrevine B, the first naphthylisoquinoline alkaloid with A 5,8′-coupling site, and related compounds from Ancistrocladus abbreviatus

3. Die absoluté Konfiguration von Michellamin B, einem „dimeren”, anti-HIV-aktiven Naphthylisochinolin-Alkaloid

4. The Absolute Configuration of Michellamine B, a “Dimeric”, Anti-HIV-Active Naphthylisoquinoline Alkaloid

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1. Recent Advances of Applying Boron‐Reagents in Asymmetric Total Syntheses of Natural Products and Bio‐Active Molecules;Advanced Synthesis & Catalysis;2020-06-29

2. Configurational analysis by residual dipolar couplings: A critical assessment of diastereomeric differentiabilities;Chirality;2019-03-27

3. Dimeric naphthylisoquinoline alkaloids: polyketide-derived axially chiral bioactive quateraryls;Natural Product Reports;2019

4. Current Applications of Suzuki–Miyaura Coupling Reaction in The Total Synthesis of Natural Products: An update;Applied Organometallic Chemistry;2018-01-19

5. Four new phenylethanoid and flavonoid glycoside dimers from the fruits of Forsythia suspensa and their neuroprotective activities;RSC Advances;2017

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