Results 141 to 150 of about 4,376 (210)

Bioresponsive pseudoGlucosinolates (psGSLs) Release Isothiocyanates (ITCs) in the Presence of Nitroreductases. [PDF]

Chemistry
Jimidar CC, Ganskow CSG, Kagho MD, Chakrabarti A, Wiese L, Zollo M, Beutling U, Cesar LC, Morud J, Bugaj K, Brönstrup M, Sieber SA, Hacker SM, Klahn P.   +13 more
europepmc   +1 more source

Recent Advances in the Synthesis of Benzo[<i>d</i>]isothiazol-3(2<i>H</i>)-One and Benzo[<i>e</i>][1,3]Thiazin-4-One Derivatives. [PDF]

Molecules
He Y, Yuan D, Yang K, Li B.
europepmc   +1 more source

Thioimidates provide general access to thioamide, amidine, and imidazolone peptide-bond isosteres. [PDF]

Methods Enzymol
Byerly-Duke J, O'Brien EA, Wall BJ, VanVeller B.   +3 more
europepmc   +1 more source

Efficient Approaches to the Design of Six-Membered Polyazacyclic Compounds-Part 1: Aromatic Frameworks. [PDF]

Molecules
Gyrgenova EA, Titova YY, Ivanov AV.
europepmc   +1 more source

Synthesis of Heteroleptic Amidinato Calcium Halides via the In-Situ Grignard Addition Method (iGAM) Complementing the Metalation of Amidines. [PDF]

Chemistry
Sengupta S, Broek M, Köhler P, Westerhausen M.   +3 more
europepmc   +1 more source

Synthesis of amidines and amidinates with m-terphenyl substituents

, 2001
Sterically demanding amidines, 'N,N''-diisopropyl-2,4,6-triphenylbenzam idine 2.6a, and 'N,N''-dicyclohexyl-2,4,6-triphenylbenza midine 2.6b, have been prepared via reaction of the corresponding carbodiimide with 2,4,6-triphenylphenyllithium (generated 'in situ via' lithiation of 2,4,6-triphenylbromobenzene).
Abeysekera, Sumudu Deepa
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Amidine Nitrosation

The Journal of Organic Chemistry, 2004
The acidic nitrosation chemistry of nine acyclic secondary and tertiary amidines (Ph-N=C(R(1))NR(2)R(3); R(1) = H, CH(3), Ph; R(2), R(3) = H, Ph or (CH(3))(2) or C(CH(2))(4)) and several N-acylamidines was investigated. The principal nitrosation products were amides derived from the amino moiety and compounds derived from the benzenediazonium ion ...
Richard N, Loeppky, Hongbin, Yu
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Electrochemical behavior of amidine hydrochlorides and amidines

Canadian Journal of Chemistry, 1995
The electrochemical behavior of N,N-dimethyl-N′-phenylformamidine hydrochloride was studied on a platinum electrode. The oxidation peak at +0.90 V vs. Ag/Ag+ 0.01 M (in CH3CN −0.1 M LiClO4) was assigned to the oxidation of the chloride anion. N,N-Dimethyl-N′-(4-chlorophenyl)formamidine and N,N-dimethyl-N′-(2-chlorophenyl)formamidine were isolated from
Benoit Daoust, Jean Lessard
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SYNTHESIS OF AMIDINE AND BIS AMIDINE PERCURSORS

Phosphorus, Sulfur, and Silicon and the Related Elements, 2001
Abstract The reactions of substituted o-phenylene diamines, o-aminophenol, o-aminothiophenol, 3,4-diaminopyridine with p-cyanobenzaldehyde by refluxing in nitrobenzene gave corresponding benzimidazole, benzoxazole, benzthiazole and imidazopyridine derivatives Ia,b, II, III, and IV, respectively.
Nidhi Singhal, Monika Johar, J. W Lown, S. M Sondhi   +3 more
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