The ‘valence tautomers’ of o-iodosobenzoic acid: the case of 4-pentyl-2-iodosobenzoic acid

1998 ◽  
pp. 1559-1560 ◽  
Author(s):  
Robert A. Moss ◽  
T. J. Emge
ChemInform ◽  
2010 ◽  
Vol 29 (47) ◽  
pp. no-no
Author(s):  
R. A. MOSS ◽  
S. VIJAYARAGHAVAN ◽  
T. J. EMGE

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1897
Author(s):  
Hideyasu China ◽  
Nami Kageyama ◽  
Hotaka Yatabe ◽  
Naoko Takenaga ◽  
Toshifumi Dohi

We report a convenient and practical method for the preparation of nonexplosive cyclic hypervalent iodine(III) oxidants as efficient organocatalysts and reagents for various reactions using Oxone® in aqueous solution under mild conditions at room temperature. The thus obtained 2-iodosobenzoic acids (IBAs) could be used as precursors of other cyclic organoiodine(III) derivatives by the solvolytic derivatization of the hydroxy group under mild conditions of 80 °C or lower temperature. These sequential procedures are highly reliable to selectively afford cyclic hypervalent iodine compounds in excellent yields without contamination by hazardous pentavalent iodine(III) compound.


Author(s):  
Yannick Schulte ◽  
Blaise L. Geoghegan ◽  
Christoph Helling ◽  
Christoph Wölper ◽  
Gebhard Haberhauer ◽  
...  
Keyword(s):  

2016 ◽  
Vol 40 (12) ◽  
pp. 10300-10304 ◽  
Author(s):  
Raktani Bikshapathi ◽  
Parvathaneni Sai Prathima ◽  
Vaidya Jayathirtha Rao

An efficient, eco-friendly protocol for selective oxidation of primary and secondary Baylis–Hillman alcohols to the corresponding carbonyl compounds in high yields has been developed with 2-iodosobenzoic acid (IBA).


2014 ◽  
Vol 69 (11-12) ◽  
pp. 1088-1096 ◽  
Author(s):  
Jan-Niklas Schäckermann ◽  
Thomas Lindel

Abstract The first enantioselective synthesis of a photoreactive (R)-β-phenylalanine is described. In the key step, m-diazirinyl-substituted benzaldehyde is converted to a chiral sulfinimine in a Ti(OEt)4- mediated reaction, followed by diastereoselective enolate addition. The absolute configuration of photo (R)-β-phenylalanine was confirmed by Mosher analysis. The photo amino acid proved to be thermally stable under standard laboratory conditions. Irradiation in toluene afforded cycloheptatriene=norcaradiene valence tautomers, together with carbene benzylation. Quantumchemical calculations indicate a small triplet-singlet gap.


2009 ◽  
Vol 87 (4) ◽  
pp. 533-538 ◽  
Author(s):  
Thomas J. O’Sullivan ◽  
Brandon Djukic ◽  
Paul A. Dube ◽  
Martin T. Lemaire

The synthesis and characterization of two new 2,2′-bipyridine ligands containing 3-ethynylthiophene and 3,3′-diethynyl-2,2′-bithiophene substituents is presented, along with the preparation, electronic, and magnetic properties of mono- and bimetallic cobalt-semiquinone valence tautomers containing these ligands.


1988 ◽  
Vol 43 (1-2) ◽  
pp. 77-83 ◽  
Author(s):  
Iwan Bissig ◽  
René A. Brunisholz ◽  
Franz Suter ◽  
Richard J. Cogdell ◽  
Herbert Zuber

Spectrally pure B 800-850 light harvesting complexes of Rhodopseudomonas acidophila 7750 were prepared by chromatography of LDAO-solubilised photosynthetic membranes on Whatmann DE-52 ion exchange resin. Two low molecular mass polypeptides (α, β) have been isolated by organic solvent extraction of the lyophilised B 800-850 light harvesting complexes. Their primary structures were determined by liquid phase sequencer runs, by the sequence analyses of C-terminal o-iodosobenzoic acid fragments, by hydrazinolysis and by carboxypeptidase degradation. B 800-850-a consists of 53 amino acids and is 45.3% and 50.9% homologous to the B 800-850- a antenna polypeptides of Rhodobacter sphaeroides and Rhodobacter capsulatus, respectively. The second very short polypeptide (B800-850-β, 41 amino acids) is 61.0% and 56.1% homologous to the corresponding polypeptides of Rb. sphaeroides and Rb. capsulatus. The molar ratio of the two polypeptides is about 1:1. Both polypeptides show a hydrophilic N-terminal domain, a very hydrophobic central domain and a short C-terminal domain. In both polypeptides the typical His residues, identified in all antenna polypeptides of purple nonsulphur bacteria as possible bacteriochlorophyll binding sites, were found


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