Diversity-oriented synthesis of dihydrobenzoxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Bibliographic citation
-
Diversity-oriented synthesis of dihydrobenzoxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization ; volume:10 ; pages:209-212
Beilstein journal of organic chemistry ; 10, 209-212
- Classification
-
Chemie
- DOI
-
10.3762/bjoc.10.16
- URN
-
urn:nbn:de:101:1-201501027945
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:23 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)
Site‐Selective Protein Conjugation by a Multicomponent Ugi Reaction
Multicomponent cyclization strategies to novel conformationally constrained peptides
Chemical Production of Cytotoxic Bispecific Antibodies Using the Ugi Multicomponent Reaction
Coupling Interrupted Fischer and Multicomponent Joullié‐Ugi to Chase Chemical Diversity: from Batch to Sustainable Flow Synthesis of Peptidomimetics
Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines
Modular Divergent Synthesis of Indole Alkaloid Derivatives by an Atypical Ugi Multicomponent Reaction
Ugi, Luise
Ugi, Oskar
Ugi, Ivar
Ugi, Richard
Ugi, Wilhelm
Ugi, Christian
Site‐Selective Protein Conjugation by a Multicomponent Ugi Reaction
Multicomponent cyclization strategies to novel conformationally constrained peptides
Chemical Production of Cytotoxic Bispecific Antibodies Using the Ugi Multicomponent Reaction
Coupling Interrupted Fischer and Multicomponent Joullié‐Ugi to Chase Chemical Diversity: from Batch to Sustainable Flow Synthesis of Peptidomimetics
Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines
Modular Divergent Synthesis of Indole Alkaloid Derivatives by an Atypical Ugi Multicomponent Reaction
Ugi, Luise
Ugi, Oskar
Ugi, Ivar
Ugi, Richard
Ugi, Wilhelm
Ugi, Christian
Site‐Selective Protein Conjugation by a Multicomponent Ugi Reaction
Multicomponent cyclization strategies to novel conformationally constrained peptides
Chemical Production of Cytotoxic Bispecific Antibodies Using the Ugi Multicomponent Reaction
Coupling Interrupted Fischer and Multicomponent Joullié‐Ugi to Chase Chemical Diversity: from Batch to Sustainable Flow Synthesis of Peptidomimetics
Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines
Modular Divergent Synthesis of Indole Alkaloid Derivatives by an Atypical Ugi Multicomponent Reaction
Ugi, Luise
Ugi, Oskar
Ugi, Ivar
Ugi, Richard
Ugi, Wilhelm