N-H bond formation
Mixed- Ligand Phosphine and Arsine Complexes of Ruthenium (III) Ligated by Heterocyclic Thioamide
5
1,3 Bis{(E) [4 (dimethylamino)benzylidene]amino}propan 2 ol: chain structure formation via an O—H⋯N hydrogen bond
13
Dichloro(di 2 pyridylamine)gold(III) chloride
6
C N bond formation in the reaction of nitrogen ions N+ with benzene molecules
6
O vs N protonation of 1 dimethylaminonaphthalene 8 ketones : formation of a peri N–C bond or a hydrogen bond to the pi electron density of a carbonyl group
13
C–N bond formation between alcohols and amines using an iron cyclopentadienone catalyst
5
1 [(5 Chloro 2 hydroxyphenyl)(phenyl)methyl] 2 (2 pyridyl) 1H benzimidazole
11
N′ [(1E) 1 (2 Fluorophenyl)ethylidene]pyridine 3 carbohydrazide
7
3,6 Dioxaoctane 1,8 diammonium bis(trichloroacetate)
6
Syntheses and Structure Elucidations of Ternary Metal [Cu/Co] Complexes with Nucleic Acid Constituents
16
International Journal of Research in Engineering and Science (IJRES) ISSN (Online): 2320-9364, ISSN (Print): 2320-9356 www.ijres.org Volume 6 Issue 4 Ver. I ǁ 2018 ǁ PP. 54-65 The Effect Of Proton And Water Molecule On Watson Crick Hydrogen Bonds And The Formation Of Cytosine(C)- Thymine(T) Base Pairs.
12
Crystal structure of bis[(phenylmethanamine κN)(phthalocyaninato κ4N)zinc] phenylmethanamine trisolvate
24
The importance of the N–H bond in Ru/TsDPEN complexes for asymmetric transfer hydrogenation of ketones and imines
6
4 (3 Methylanilino)pyridine 3 sulfonamide
10
Risperidone chloride 2 5 hydrate: a new crystalline form
15
Synthesis, crystal structure, and non covalent interactions in ethyl 4 hydrazinobenzoate hydrochloride
25
(E) 2 [1 (1 Benzothiophen 3 yl)ethylidene]hydrazinecarbothioamide methanol hemisolvate
15
cis Bis(butylamine κN)bis[sulfadiazine(1−) κ2N,N′]copper(II) pentahydrate
8
3 Azaspiro[5 5]undecane 2,4 dione
7
Different intra and intermolecular hydrogen bonding patterns in (3S,4aS,8aS) 2 [(2R,3S) 3 (2,5 X2 benzamido) 2 (2,5 X2 benzoyloxy) 4 phenylbutyl] N tert butyldecahydroisoquinoline 3 carboxamides (X = H or Cl): compounds with moderate aspartyl protease inhibition activity
22