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A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors

Viktor Fedorovich Zheltukhin 1
Viktor Fedorovich Zheltukhin
Kirill Evgenievich Metlushka 1
Kirill Evgenievich Metlushka
Dilyara Nurgalievna Sadkova 1
Dilyara Nurgalievna Sadkova
Charles E McKenna 2
Charles E McKenna
Boris Anatol'evich Kashemirov 2
Boris Anatol'evich Kashemirov
Vladimir Alekseevich Alfonsov 1
Vladimir Alekseevich Alfonsov
Published 2007-06-22
CommunicationVolume 17, Issue 4, 239-240
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Zheltukhin V. F. et al. A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors // Mendeleev Communications. 2007. Vol. 17. No. 4. pp. 239-240.
GOST all authors (up to 50) Copy
Zheltukhin V. F., Metlushka K. E., Sadkova D. N., McKenna C. E., Kashemirov B. A., Alfonsov V. A. A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors // Mendeleev Communications. 2007. Vol. 17. No. 4. pp. 239-240.
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TY - JOUR
DO - 10.1016/j.mencom.2007.06.020
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.06.020
TI - A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors
T2 - Mendeleev Communications
AU - Zheltukhin, Viktor Fedorovich
AU - Metlushka, Kirill Evgenievich
AU - Sadkova, Dilyara Nurgalievna
AU - McKenna, Charles E
AU - Kashemirov, Boris Anatol'evich
AU - Alfonsov, Vladimir Alekseevich
PY - 2007
DA - 2007/06/22
PB - Mendeleev Communications
SP - 239-240
IS - 4
VL - 17
ER -
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@article{2007_Zheltukhin,
author = {Viktor Fedorovich Zheltukhin and Kirill Evgenievich Metlushka and Dilyara Nurgalievna Sadkova and Charles E McKenna and Boris Anatol'evich Kashemirov and Vladimir Alekseevich Alfonsov},
title = {A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors},
journal = {Mendeleev Communications},
year = {2007},
volume = {17},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.06.020},
number = {4},
pages = {239--240},
doi = {10.1016/j.mencom.2007.06.020}
}
MLA
Cite this
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Zheltukhin, Viktor Fedorovich, et al. “A new approach to the synthesis of benzylidene derivatives of 1-(α-aminobenzyl)-2-naphthols (Betti bases), promising chiral inductors.” Mendeleev Communications, vol. 17, no. 4, Jun. 2007, pp. 239-240. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.06.020.

Abstract

A new approach to the synthesis of precursors of Betti bases is described, in which β-naphthol reacts with 1,3,5-triaryl- 2,4-diazapenta-1,4-dienes (3:2) in refluxing benzene.

References

1.
CHIRAL PHARMACEUTICALS
STINSON S.C.
Chemical & Engineering News, 2001
6.
The Application of Chiral Aminonaphthols in the Enantioselective Addition of Diethylzinc to Aryl Aldehydes
Liu D., Zhang L., Wang Q., Da C., Xin Z., Wang R., Choi M.C., Chan A.S.
Organic Letters, 2001
10.
10.1016/j.mencom.2007.06.020_bib3_8
Li
Chem., 2002
13.
An improved synthesis of chiral 1-[α-(1-azacycloalkyl)benzyl]-2-naphthols
Xu X., Lu J., Dong Y., Li R., Ge Z., Hu Y.
Tetrahedron Asymmetry, 2004
15.
Stereoelectronic effects in ring-chain tautomerism of 1,3-diarylnaphth[1,2-e][1,3]oxazines and 3-alkyl-1-arylnaphth[1,2-e][1,3]oxazines.
Szatmári I., Martinek T.A., Lázár L., Koch A., Kleinpeter E., Neuvonen K., Fülöp F.
Journal of Organic Chemistry, 2004
16.
10.1016/j.mencom.2007.06.020_bib3_14
Xu
Synlett., 2004
17.
Transformation reactions of the betti base analog aminonaphthols
Szatmári I., Hetényi A., Lázár L., Fülöp F.
Journal of Heterocyclic Chemistry, 2004
20.
Highly Enantioselective Phenyl Transfer to Aryl Aldehydes Catalyzed by Easily Accessible Chiral Tertiary Aminonaphthol
Ji J., Wu J., Au-Yeung T.T., Yip C., Haynes R.K., Chan A.S.
Journal of Organic Chemistry, 2005
21.
10.1016/j.mencom.2007.06.020_bib4
Betti
Gazz. Chim. Ital., 1900
22.
10.1016/j.mencom.2007.06.020_bib5
Betti
Org. Synth. Coll. Vol., 1941
26.
10.1016/j.mencom.2007.06.020_bib7_1
Mamaev
Izv. Akad. Nauk SSSR, Ser. Khim., 1965
27.
10.1016/j.mencom.2007.06.020_bib7_2
Betti
Gazz. Chim. Ital., 1903
29.
10.1016/j.mencom.2007.06.020_bib7_4
Betti
Gazz. Chim. Ital., 1901
31.
THE RESOLUTION OF 1-(ALPHA-1-PIPERIDYLBENZYL)-2-NAPHTHOL1
Brode W.R., Littman J.B.
Journal of the American Chemical Society, 1930
32.
10.1016/j.mencom.2007.06.020_bib8_1
Sachs
Ber. Dtsch. Chem. Ges., 1904
33.
2,4-Diazapentadienes. I. Prototropy, Cyclization, and Addition–Elimination
Hunter D.H., Sim S.K.
Canadian Journal of Chemistry, 1972
34.
10.1016/j.mencom.2007.06.020_bib8_3
Lozinskaya
Izv. Akad. Nauk, Ser. Khim., 2003