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Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene

Eduard Evgen'evich Nifantyev 1
Eduard Evgen'evich Nifantyev
, 
Vera Ivanovna Maslennikova 1
Vera Ivanovna Maslennikova
, 
Lyudmila Vital'evna Shelenkova 1
Lyudmila Vital'evna Shelenkova
, 
Irina Ivanovna Levina 2
Irina Ivanovna Levina
, 
Dmitrii Mikhailovich Polekhin 1
Dmitrii Mikhailovich Polekhin
10.1016/j.mencom.2009.03.017
Published 2009-03-10
Communication , Volume 19, Issue 2, 101-102
4
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Nifantyev E. E. et al. Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene // Mendeleev Communications. 2009. Vol. 19. No. 2. pp. 101-102.
GOST all authors (up to 50) Copy
Nifantyev E. E., Maslennikova V. I., Shelenkova L. V., Levina I. I., Polekhin D. M. Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene // Mendeleev Communications. 2009. Vol. 19. No. 2. pp. 101-102.
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TY - JOUR
DO - 10.1016/j.mencom.2009.03.017
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.03.017
TI - Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene
T2 - Mendeleev Communications
AU - Nifantyev, Eduard Evgen'evich
AU - Maslennikova, Vera Ivanovna
AU - Shelenkova, Lyudmila Vital'evna
AU - Levina, Irina Ivanovna
AU - Polekhin, Dmitrii Mikhailovich
PY - 2009
DA - 2009/03/10
PB - Mendeleev Communications
SP - 101-102
IS - 2
VL - 19
ER -
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@article{2009_Nifantyev,
author = {Eduard Evgen'evich Nifantyev and Vera Ivanovna Maslennikova and Lyudmila Vital'evna Shelenkova and Irina Ivanovna Levina and Dmitrii Mikhailovich Polekhin},
title = {Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene},
journal = {Mendeleev Communications},
year = {2009},
volume = {19},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.03.017},
number = {2},
pages = {101--102},
doi = {10.1016/j.mencom.2009.03.017}
}
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Nifantyev, Eduard Evgen'evich, et al. “Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene.” Mendeleev Communications, vol. 19, no. 2, Mar. 2009, pp. 101-102. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.03.017.

Abstract

The reaction of 2,2’,7,7’-tetrahydroxydinaphthylmethane with aniline in the presence of aniline salts involves the rupture of C–C bonds and the elimination of a methylene bridge and is completed by the formation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene, the phosphorylation of which with 2-chloro-1,3,2-dioxaphosphinane and dichloroisopropyl phosphite yields original polycyclic phosphamide architectures.

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