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Metal-mediated post-Ugi transformations for the construction of diverse heterocyclic scaffolds.
Sharma, Upendra K; Sharma, Nandini; Vachhani, Dipak D; Van der Eycken, Erik V.
Affiliation
  • Sharma UK; Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, B-3001, Leuven, Belgium. erik.vandereycken@chem.kuleuven.be.
Chem Soc Rev ; 44(7): 1836-60, 2015 Apr 07.
Article in En | MEDLINE | ID: mdl-25652577
ABSTRACT
The Ugi-4CR is by far one of the most successful multicomponent reactions leading to high structural diversity and molecular complexity. However, the reaction mostly affords a linear peptide backbone, enabling post-Ugi transformations as the only solution to rigidify the Ugi-adduct into more drug like species. Not surprisingly, the development of these transformations, leading to new structural frameworks, has expanded rapidly over the last few years. As expected, palladium-catalyzed reactions have received the foremost attention, yet other metals, particularly gold complexes, are fast catching up. This tutorial review outlines the developments achieved in the past decade, highlighting the modifications that are performed in a sequential or domino fashion with emphasis on major concepts, synthetic applications of the derived products as well as mechanistic aspects.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Heterocyclic Compounds / Metals Language: En Journal: Chem Soc Rev Year: 2015 Type: Article Affiliation country: Belgium

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Heterocyclic Compounds / Metals Language: En Journal: Chem Soc Rev Year: 2015 Type: Article Affiliation country: Belgium