Results 41 to 50 of about 81,520 (144)
Observation of different reactivities of para and ortho-water towards trapped diazenylium ions [PDF]
Nature Communications, 2018 Water is one of the most fundamental molecules in chemistry, biology and astrophysics. It exists as two distinct nuclear-spin isomers, para- and ortho-water, which do not interconvert in isolated molecules.
Ardita Kilaj +5 more
semanticscholar +1 more source
Journal of Surfactants and Detergents, Volume 27, Issue 2, Page 259-267, March 2024.Abstract Tetradecyltrimethylammonium (TTA+) benzoate surfactants have a range of CMC values dependent on the substituent effects of the benzoate counterions. Twenty‐three TTA+/X‐benzoate CMC values were determined by conductivity and surface tension. The 12 TTA+/para‐ and meta‐benzoate and the unsubstituted benzoate CMC values yield a correlation to ...
Steven J. Bachofer
wiley +1 more source
Environmental Microbiology Reports, Volume 16, Issue 1, February 2024.Novosphingobium sp. MBES04 possesses a unique ability to sense lignin fragments by producing phenylpropanones which induce specific transcriptional responses. The strongly induced clusters involved in energy production by oxidative degradation and multidrug resistance. This adaptation may be a survival strategy, whereby the strain MBES04 preferentially
Eri Kumagawa +5 more
wiley +1 more source
Sulfenamide-enabled ortho thiolation of aryl iodides via palladium/norbornene cooperative catalysis
Nature Communications, 2019 Poly-substituted aromatic sulfur compounds are widely found in pharmaceuticals, agrochemicals and organic materials. However, the position that a sulfur moiety can be introduced to is largely restricted to a pre-functionalized site; otherwise, use of ...
Renhe Li +4 more
semanticscholar +1 more source
Hydrogen Bond Directed ortho‐Selective C−H Borylation of Secondary Aromatic Amides
Angewandte Chemie, 2019 Reported is an iridium catalyst for ortho‐selective C−H borylation of challenging secondary aromatic amide substrates, and the regioselectivity is controlled by hydrogen‐bond interactions.
Shao‐Tao Bai, C. Bheeter, J. Reek
semanticscholar +1 more source
Nitrobenzoates and Aminobenzoates Are Chemoattractants for Pseudomonas Strains
Applied and Environmental Microbiology, 2004 R. Parales
semanticscholar +1 more source
Conjugation and excretion of the amino and acetamido benzoic acids.
American Journal of Physiology, 1959 P. Knoefel, K. Huang, A. Dispopoulos
semanticscholar +1 more source
Hydrogen Exchange Reaction of Aminobenzoic Acid. II. Platinum catalyzed Hydrogen Exchange Reaction
, 1972 M. Matsuo +3 more
semanticscholar +1 more source