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Preparative scalable method for the synthesis of cyclic and acyclic acetals of chloropropiolaldehyde and their transformation into acetals of lithiumpropiolaldehyde
by
Shilova, O. S.
, Artyushin, O. I.
, Druzina, A. A.
, Koldobskii, A. B.
in
Acetals
/ Brief Communications
/ Butyllithium
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Chloroformate
/ Inorganic Chemistry
/ Nucleophiles
/ Organic Chemistry
/ Synthesis
2024
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Preparative scalable method for the synthesis of cyclic and acyclic acetals of chloropropiolaldehyde and their transformation into acetals of lithiumpropiolaldehyde
by
Shilova, O. S.
, Artyushin, O. I.
, Druzina, A. A.
, Koldobskii, A. B.
in
Acetals
/ Brief Communications
/ Butyllithium
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Chloroformate
/ Inorganic Chemistry
/ Nucleophiles
/ Organic Chemistry
/ Synthesis
2024
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Preparative scalable method for the synthesis of cyclic and acyclic acetals of chloropropiolaldehyde and their transformation into acetals of lithiumpropiolaldehyde
by
Shilova, O. S.
, Artyushin, O. I.
, Druzina, A. A.
, Koldobskii, A. B.
in
Acetals
/ Brief Communications
/ Butyllithium
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Chloroformate
/ Inorganic Chemistry
/ Nucleophiles
/ Organic Chemistry
/ Synthesis
2024
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Preparative scalable method for the synthesis of cyclic and acyclic acetals of chloropropiolaldehyde and their transformation into acetals of lithiumpropiolaldehyde
Journal Article
Preparative scalable method for the synthesis of cyclic and acyclic acetals of chloropropiolaldehyde and their transformation into acetals of lithiumpropiolaldehyde
2024
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Overview
A simple two-step and easily scalable method for the synthesis of cyclic and acyclic acetals of chloropropiolaldehyde was developed. They readily reacted with
n
-butyllithium to give stable crystalline acetals of lithiumpropiolaldehyde, which, being strong nucleophiles, reacted with chlorotrimethylsilane, chlorotrimethylstannane, and methyl chloroformate to form bifunctional acetylenes in high yields.
Publisher
Springer US,Springer Nature B.V
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