Direct C–H borylation of vinylporphyrins <i>via</i> copper catalysis-Reference-Cited by-同舟云学术

Direct C–H borylation of vinylporphyrins via copper catalysis

Published:2022 Issue:9 Volume:20 Page:1926-1932
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Belyaev Evgeny S.¹,Kozhemyakin Grigory L.¹,Tyurin Vladimir S.¹^ORCID,Frolova Victoria V.¹,Lonin Ivan S.¹,Ponomarev Gelii V.²,Buryak Aleksey K.¹,Zamilatskov Ilya A.¹

Affiliation:

1. Frumkin Institute of Physical Chemistry and Electrochemistry Russian Academy of Sciences, Leninsky prospect, 31-4, Moscow, 119071, Russian Federation

2. Research Institute of Biomedical Chemistry, Pogodinskaya str., 10-8, 119121, Moscow, Russian Federation

Abstract

A method of direct borylation of vinyl-substituted porphyrinoids (porphyrins and chlorins) has been developed based on the copper catalyzed vinylic C–H activation.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D1OB02005F

Reference35 articles.

1. The Suzuki-Miyaura reaction after the Nobel prize

2. Synthesis of Doubly β-to-β 1,3-Butadiyne-Bridged Diporphyrins: Enforced Planar Structures and Large Two-Photon Absorption Cross Sections

3. Porphyrin “Lego Block” Strategy To Construct Directly meso-β Doubly Linked Porphyrin Rings