Development of a stereoselective Ugi reaction starting from an oxanorbornene β-amino acid derivative-Reference-Cited by-同舟云学术

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Development of a stereoselective Ugi reaction starting from an oxanorbornene β-amino acid derivative

Published:2012 Issue:19 Volume:10 Page:3819
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Banfi Luca,Basso Andrea,Chiappe Cinzia,De Moliner Fabio,Riva Renata,Sonaglia Lorenzo

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB25060H

Reference25 articles.

1. Advances in Solution- and Solid-Phase Synthesis toward the Generation of Natural Product-like Libraries

2. Targeting Oncogenic Protein-Protein Interactions by Diversity Oriented Synthesis and Combinatorial Chemistry Approaches

3. A Marriage of Convenience: Combining the Power of Isocyanide‐Based Multicomponent Reactions with the Versatility of (Hetero)norbornene Chemistry

4. U-4C-3CR versus U-5C-4CR and stereochemical outcomes using suitable bicyclic β-amino acid derivatives as bifunctional components in the Ugi reaction

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1. A Half‐Century of the Ugi Reaction: Modified Variants;Organic Reactions;2023-05-05

2. Multicomponent Synthesis: Cohesive Integration of Green Chemistry Principles;Methods in Pharmacology and Toxicology;2021-12-14

3. A concise review on the stereoselective synthesis of chiral α-bisamides using stereoselective Ugi-type reaction;Arkivoc;2021-07-06

4. Facile synthesis and biological evaluation of tryptamine-piperazine-2,5-dione conjugates as anticancer agents;RSC Advances;2021

5. Controlling the stereochemistry in 2-oxo-aldehyde-derived Ugi adducts through the cinchona alkaloid-promoted electrophilic fluorination;Beilstein Journal of Organic Chemistry;2020-08-11

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