ChemInform Abstract: BORON-NITROGEN COMPOUNDS. 86. SOME NEW ORGANOBORON-NITROGEN HETEROCYCLES

1981 ◽  
Vol 12 (9) ◽  
Author(s):  
J. BIELAWSKI ◽  
K. NIEDENZU
1964 ◽  
Vol 3 (8) ◽  
pp. 1077-1079 ◽  
Author(s):  
Kurt Niedenzu ◽  
Peter Fritz ◽  
John W. Dawson

1984 ◽  
Vol 23 (23) ◽  
pp. 3713-3716 ◽  
Author(s):  
Kurt Niedenzu ◽  
Philipp M. Niedenzu

2007 ◽  
Vol 62 (2) ◽  
pp. 220-224 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Oleg L. Tok

Boron-nitrogen compounds were studied with respect to indirect nuclear 15N-11B spin-spin coupling (1J(15N,11B)). Some new experimental data were determined for aminoboranes and tetra-Npyrrolylborate, and a variety of compounds with B-N single, double and triple bonds were examined using DFT methods for the calculation of 1J(15N,11B) at the B3LYP/6-311+G(d,p) level of theory. The calculations predict magnitude and sign of 1J(15N,11B) reasonably well, and the Fermi contact term was found to be dominant. A positive sign of 1J(15N,11B) was calculated in the case of 1-azacloso- dodecaborane(12), in contrast to all other compounds studied.


1967 ◽  
Vol 55 (3_4) ◽  
pp. 224-224
Author(s):  
M. Baudler

1969 ◽  
Vol 0 (13) ◽  
pp. 775-776 ◽  
Author(s):  
Iring Geisler ◽  
Heinrich Nöth

Molecules ◽  
2020 ◽  
Vol 25 (15) ◽  
pp. 3508
Author(s):  
Carme Masdeu ◽  
Maria Fuertes ◽  
Endika Martin-Encinas ◽  
Asier Selas ◽  
Gloria Rubiales ◽  
...  

Heterocyclic nitrogen compounds, including fused 1,5-naphthyridines, have versatile applications in the fields of synthetic organic chemistry and play an important role in the field of medicinal chemistry, as many of them have a wide range of biological activities. In this review, a wide range of synthetic protocols for the construction of this scaffold are presented. For example, Friedländer, Skraup, Semmlere-Wolff, and hetero-Diels-Alder, among others, are well known classical synthetic protocols used for the construction of the main 1,5-naphthyridine scaffold. These syntheses are classified according to the nature of the cycle fused to the 1,5-naphthyridine ring: carbocycles, nitrogen heterocycles, oxygen heterocycles, and sulphur heterocycles. In addition, taking into account the aforementioned versatility of these heterocycles, their reactivity is presented as well as their use as a ligand for metal complexes formation. Finally, those fused 1,5-naphthyridines that present biological activity and optical applications, among others, are indicated.


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