Stereoselective Robinson Annulation Enables Access to Potent and Selective Salvinorin Analogs
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Stereoselective Robinson Annulation Enables Access to Potent and Selective Salvinorin Analogs ; volume:19 ; number:10 ; year:2023 ; pages:1035
Synfacts ; 19, Heft 10 (2023), 1035
- Classification
-
Chemie
- DOI
-
10.1055/s-0042-1752023
- URN
-
urn:nbn:de:101:1-2023110210204190200314
- Rights
-
Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Other Objects (12)
Stereoselective synthesis and neurobiological profiling of parthenolide and analogs
A Stereoselective Synthesis of 4′‐ α ‐Fluoro‐methyl Carbocyclic Nucleoside Analogs
(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones
(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones
Dynamic stereoselective annulation via aldol-oxa-cyclization cascade reaction to afford spirooxindole pyran polycycles
Die Annulation
Die Annulation
Diversity Oriented Synthesis of Novel Xanthones Reveal Potent Doxorubicin‐Inspired Analogs
Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation
Inverse hydride shuttle catalysis enables the stereoselective one-step synthesis of complex frameworks
The Robinson Annulation & Amines
Optimized and convergent synthesis of potent anti-malarial aminoquinoline compounds: easy access to analogs
Stereoselective synthesis and neurobiological profiling of parthenolide and analogs
A Stereoselective Synthesis of 4′‐ α ‐Fluoro‐methyl Carbocyclic Nucleoside Analogs
(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones
(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones
Dynamic stereoselective annulation via aldol-oxa-cyclization cascade reaction to afford spirooxindole pyran polycycles
Die Annulation
Die Annulation
Diversity Oriented Synthesis of Novel Xanthones Reveal Potent Doxorubicin‐Inspired Analogs
Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation
Inverse hydride shuttle catalysis enables the stereoselective one-step synthesis of complex frameworks
The Robinson Annulation & Amines
Optimized and convergent synthesis of potent anti-malarial aminoquinoline compounds: easy access to analogs
Stereoselective synthesis and neurobiological profiling of parthenolide and analogs
A Stereoselective Synthesis of 4′‐ α ‐Fluoro‐methyl Carbocyclic Nucleoside Analogs
(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones
(4+3) Annulation of Donor‐Acceptor Cyclopropanes and Azadienes: Highly Stereoselective Synthesis of Azepanones
Dynamic stereoselective annulation via aldol-oxa-cyclization cascade reaction to afford spirooxindole pyran polycycles
Die Annulation
Die Annulation
Diversity Oriented Synthesis of Novel Xanthones Reveal Potent Doxorubicin‐Inspired Analogs
Stereoselective synthesis of fused tetrahydroquinazolines through one-pot double [3 + 2] dipolar cycloadditions followed by [5 + 1] annulation
Inverse hydride shuttle catalysis enables the stereoselective one-step synthesis of complex frameworks
The Robinson Annulation & Amines