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Synthesis of non-symmetrical triarylphosphine oxide with fluorophore groups
by
Bykhovskaya, O. V.
, Kudryavtsev, I. Yu
, Pasechnik, M. P.
, Baulina, T. V.
, Brel, V. K.
in
Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Full Articles
/ Inorganic Chemistry
/ Organic Chemistry
2024
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Synthesis of non-symmetrical triarylphosphine oxide with fluorophore groups
by
Bykhovskaya, O. V.
, Kudryavtsev, I. Yu
, Pasechnik, M. P.
, Baulina, T. V.
, Brel, V. K.
in
Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Full Articles
/ Inorganic Chemistry
/ Organic Chemistry
2024
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Synthesis of non-symmetrical triarylphosphine oxide with fluorophore groups
by
Bykhovskaya, O. V.
, Kudryavtsev, I. Yu
, Pasechnik, M. P.
, Baulina, T. V.
, Brel, V. K.
in
Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Full Articles
/ Inorganic Chemistry
/ Organic Chemistry
2024
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Synthesis of non-symmetrical triarylphosphine oxide with fluorophore groups
Journal Article
Synthesis of non-symmetrical triarylphosphine oxide with fluorophore groups
2024
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Overview
The Mitsunobu reaction of tris(2-hydroxyphenyl)phosphine oxide with
N
-(3-hydroxypropyl)-4-nitro-1,8-naphthalimide resulted in alkylation of only two phenolic groups. The aromatic nitro groups of the synthesized product were replaced by the BuNH groups by the reaction with butylamine. The synthesized product exhibited fluorophore properties.
Publisher
Springer US
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