Intermolecular Formyloxyarylation of Alkenes by Photoredox Meerwein Reaction

Chang-Jiang Yao; Qiu Sun; Namrata Rastogi; Burkhard König

doi:10.1021/acscatal.5b00314

Intermolecular Formyloxyarylation of Alkenes by Photoredox Meerwein Reaction

ACS Catalysis ◽

10.1021/acscatal.5b00314 ◽

2015 ◽

Vol 5 (5) ◽

pp. 2935-2938 ◽

Cited By ~ 45

Author(s):

Chang-Jiang Yao ◽

Qiu Sun ◽

Namrata Rastogi ◽

Burkhard König

Keyword(s):

Meerwein Reaction

About possibility of the triplet mechanism of the Meerwein reaction

Journal of Molecular Structure THEOCHEM ◽

10.1016/j.theochem.2010.04.025 ◽

2010 ◽

Vol 952 (1-3) ◽

pp. 1-7 ◽

Cited By ~ 18

Author(s):

Sergey V. Bondarchuk ◽

Boris F. Minaev

Keyword(s):

Triplet Mechanism ◽

Meerwein Reaction

Chloride based ionic liquids as promoting agents for Meerwein reaction in solventless conditions

Tetrahedron Letters ◽

10.1016/j.tetlet.2006.04.072 ◽

2006 ◽

Vol 47 (27) ◽

pp. 4759-4762 ◽

Cited By ~ 24

Author(s):

Piero Mastrorilli ◽

Cosimo F. Nobile ◽

Nicola Taccardi

Keyword(s):

Ionic Liquids ◽

Meerwein Reaction

Correction. The Meerwein Reaction in Amino Acid Synthesis. II. An Investigation of Twenty-one Substituted Anilines

The Journal of Organic Chemistry ◽

10.1021/jo00836a607 ◽

1970 ◽

Vol 35 (11) ◽

pp. 4004-4004

Author(s):

George H. Cleland

Keyword(s):

Amino Acid ◽

Acid Synthesis ◽

Substituted Anilines ◽

Amino Acid Synthesis ◽

Meerwein Reaction

Arylation of Unsaturated Systems by Free Radicals. VI.1The Meerwein Reaction. IV.2The Stereochemistry of the Arylation of Maleic and Fumaric Acid Derivatives

Journal of the American Chemical Society ◽

10.1021/ja01596a065 ◽

1956 ◽

Vol 78 (15) ◽

pp. 3799-3803 ◽

Cited By ~ 7

Author(s):

O. Vogl ◽

Christian S. Rondestvedt

Keyword(s):

Free Radicals ◽

Fumaric Acid ◽

Meerwein Reaction

Syntheses of monosulfonated phthalocyanines, benzonaphthoporphyrazines and porphyrins via the Meerwein reaction

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19940002767 ◽

1994 ◽

pp. 2767 ◽

Cited By ~ 53

Author(s):

Svetlana V. Kudrevich ◽

Hasrat Ali ◽

Johan E. van Lier

Keyword(s):

Meerwein Reaction

The Meerwein Reaction with p-Nitrostyrene and 2-Vinylpyridine

Journal of the American Chemical Society ◽

10.1021/ja01637a072 ◽

1954 ◽

Vol 76 (8) ◽

pp. 2259-2260 ◽

Cited By ~ 9

Author(s):

Wesley J. Dale ◽

Charles M. Ise

Keyword(s):

Meerwein Reaction

A simple and convenient synthesis of 3-arylpyran-2-ones via the Meerwein reaction

Tetrahedron Letters ◽

10.1016/j.tetlet.2015.11.076 ◽

2016 ◽

Vol 57 (1) ◽

pp. 118-121 ◽

Cited By ~ 2

Author(s):

Roman Z. Lytvyn ◽

Andriy O. Neshchadin ◽

Khrystyna Ye. Pitkovych ◽

Yuriy I. Horak ◽

Juozas V. Grazulevicius ◽

...

Keyword(s):

Meerwein Reaction ◽

Convenient Synthesis

Communications - Cuprous Chloride Catalyzed 2,4-Dichlorophenylation of Benzene in Aqueous Acetone. The Mechanism of the Meerwein Reaction.

The Journal of Organic Chemistry ◽

10.1021/jo01109a027 ◽

1956 ◽

Vol 21 (3) ◽

pp. 380-381 ◽

Cited By ~ 14

Author(s):

S. C. Dickerman ◽

K. Weiss ◽

A. K. Ingberman

Keyword(s):

Aqueous Acetone ◽

Cuprous Chloride ◽

Meerwein Reaction

ChemInform Abstract: ORGANOMETALLIC CHEMISTRY. V. MEERWEIN REACTION. III. ARYLATION OF KETONES AND THEIR DERIVATIVES

Chemischer Informationsdienst ◽

10.1002/chin.197638141 ◽

1976 ◽

Vol 7 (38) ◽

pp. no-no

Author(s):

I. AL ADEL ◽

B. ADEOTI SALAMI ◽

J. LEVISALLES ◽

H. RUDLER

Keyword(s):

Organometallic Chemistry ◽

Meerwein Reaction

Application of the Meerwein reaction of 1,4-benzoquinone to a metal-free synthesis of benzofuropyridine analogues

Beilstein Journal of Organic Chemistry ◽

10.3762/bjoc.17.79 ◽

2021 ◽

Vol 17 ◽

pp. 977-982

Author(s):

Rashmi Singh ◽

Tomas Horsten ◽

Rashmi Prakash ◽

Swapan Dey ◽

Wim Dehaen

Keyword(s):

Building Block ◽

Electrophilic Substitution ◽

Diazonium Salt ◽

Metal Free ◽

Meerwein Reaction

Several new heterocyclic systems based on a hydroxybenzofuro[2,3-b]pyridine building block were prepared. This benzofuropyridine is easily available from the Meerwein reaction of benzoquinone and a heterocyclic diazonium salt, followed by reduction and cyclization. Electrophilic substitution and further condensations give polycyclic systems, including oxazolo- and chromeno-fused analogues.