Enantioselective Synthesis of 5,5-Disubstituted Hydantoins by Brønsted Base/H-Bond Catalyst Assisted Michael Reactions of a Design Template-Reference-Cited by-同舟云学术

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Enantioselective Synthesis of 5,5-Disubstituted Hydantoins by Brønsted Base/H-Bond Catalyst Assisted Michael Reactions of a Design Template

Published:2018-04-30 Issue:28 Volume:24 Page:7217-7227
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Izquierdo Joseba¹,Etxabe Julen¹,Duñabeitia Eider¹,Landa Aitor¹^ORCID,Oiarbide Mikel¹^ORCID,Palomo Claudio¹^ORCID

Affiliation:

1. Departamento de Química Orgánica I; Universidad del País Vasco UPV/EHU; Manuel Lardizabal 3 20018 San Sebastián Spain

Funder

Secretaría de Estado de Investigación, Desarrollo e Innovación

Eusko Jaurlaritza

Euskal Herriko Unibertsitatea

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference110 articles.

1. Coumarins and antiplatelet aggregation constituents from formosan Peucedanum japonicum

2. Mauritamide A and accompanying oroidin alkaloids from the sponge agelas mauritiana

3. Biologically active metabolites from Agelas mauritiana

4. Isolation of 1-Methyl-4,5-dibromopyrrole-2-carboxylic Acid and Its 3'-(Hydantoyl)propylamide (Midpacamide) from a Marine Sponge

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4. Brønsted Base‐Catalyzed Enantioselective α‐Functionalization of Carbonyl Compounds Involving π‐Extended Enolates;The Chemical Record;2023-06-23

5. Enantioselective and Chemoselective Phosphine Oxide‐catalyzed Aldol Reactions of N ‐Unprotected Cyclic Carboxyimides;Chemistry – A European Journal;2023-02-10

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