Synthesis of Diphenylchalcogenophene Diboronic Acid Bis(pinacol) Esters and Halogen Photoelimination from Tellurium by Triplet-Triplet Annihilation-Reference-Cited by-同舟云学术

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Synthesis of Diphenylchalcogenophene Diboronic Acid Bis(pinacol) Esters and Halogen Photoelimination from Tellurium by Triplet-Triplet Annihilation

Published:2016-08-12 Issue:9 Volume:81 Page:917-921
ISSN:2192-6506
Container-title:ChemPlusChem
language:en
Short-container-title:ChemPlusChem

Author:

Li Peng-Fei¹^ORCID,Carrera Elisa I.¹^ORCID,Seferos Dwight S.¹^ORCID

Affiliation:

1. Department of Chemistry; University of Toronto; 80 St. George Toronto ON M5S 3H6 Canada

Funder

NSERC for a Discovery Accelerator Supplement, DuPont

Alfred P. Sloan Foundation

NSERC

Walter Sumner Foundation

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cplu.201600335/fullpdf

Reference90 articles.

1. Visible light photoredox catalysis: applications in organic synthesis

2. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis

3. The Artificial Leaf

4. Artificial Photosynthesis: Molecular Systems for Catalytic Water Oxidation

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1. Oxidation-Controlled, Strain-Promoted Tellurophene-Alkyne Cycloaddition (OSTAC): A Bioorthogonal Tellurophene-Dependent Conjugation Reaction;Journal of the American Chemical Society;2024-09-11

2. A new Tellurium-bearing substituted β-diketone: Synthesis and properties;Polyhedron;2023-06

3. Tellurophenes;Comprehensive Heterocyclic Chemistry IV;2022

4. Tellurophene-containing π-conjugated polymers with unique heteroatom–heteroatom interactions by post-element-transformation of an organotitanium polymer;Polymer Chemistry;2020

5. Ring Opening of π-Delocalized 2,5-Diphenyltellurophene by Chemical or Self-Sensitized Aerobic Photooxidation;Organometallics;2017-05-10

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