Studying the reactivity of alkyl substituted BODIPYs: first enantioselective addition of BODIPY to MBH carbonates
Open Access
- 5 February 2021
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Science
- Vol. 12 (12), 4503-4508
- https://doi.org/10.1039/d0sc06574a
Abstract
The first enantioselective addition of alkyl BODIPYs to Morita–Baylis–Hillman (MBH) carbonates is reported.Funding Information
- Spanish Ministry of Economy and Competitiveness (CTQ2017-85658-R)
This publication has 67 references indexed in Scilit:
- Synthesis of Meso-Halogenated BODIPYs and Access to Meso-Substituted AnaloguesOrganic Letters, 2012
- Fluorescent indicators based on BODIPYChemical Society Reviews, 2012
- Organocatalytic enantioselective methodologies using Morita–Baylis–Hillman carbonates and acetatesCatalysis Science & Technology, 2011
- 8-Alkenylborondipyrromethene dyes. General synthesis, optical properties, and preliminary study of their reactivityTetrahedron, 2011
- Modulation of the photophysical properties of BODIPY dyes by substitution at their meso position.RSC Advances, 2011
- Phenyliodine(III) Bis(trifluoroacetate) (PIFA)-Promoted Synthesis of Bodipy Dimers Displaying Unusual Redox PropertiesOrganic Letters, 2011
- High‐Resolution Single‐Turnover Mapping Reveals Intraparticle Diffusion Limitation in Ti‐MCM‐41‐Catalyzed EpoxidationAngewandte Chemie, 2010
- The Chemistry of Fluorescent Bodipy Dyes: Versatility UnsurpassedAngewandte Chemie, 2008
- BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic PropertiesChemical Reviews, 2007
- Enantioselective Synthesis of Near Enantiopure Compound by Asymmetric Autocatalysis Triggered by Asymmetric Photolysis with Circularly Polarized LightJournal of the American Chemical Society, 2005