Unsymmetrically substituted aliphatic diacetylenes

Eugen Barbu; John Tsibouklis

doi:10.1016/0040-4039(96)01025-8

Unsymmetrically substituted aliphatic diacetylenes

Eugen Barbu, John Tsibouklis

Research output: Contribution to journal › Article › peer-review

Abstract

A general method for the synthesis of pure samples of unsymmetrically disubstituted diacetylenes of the type CH3(CH2)nCCCCCH2OH (n=2,3,4,5) is described in detail. The materials could be polymerized thermally, in the liquid state.

Original language	English
Pages (from-to)	5023-5026
Journal	Tetrahedron Letters
Volume	37
Issue number	28
DOIs	https://doi.org/10.1016/0040-4039(96)01025-8
Publication status	Published - 8 Jul 1996

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10.1016/0040-4039(96)01025-8

http://linkinghub.elsevier.com/retrieve/pii/0040403996010258

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title = "Unsymmetrically substituted aliphatic diacetylenes",

abstract = "A general method for the synthesis of pure samples of unsymmetrically disubstituted diacetylenes of the type CH3(CH2)nCCCCCH2OH (n=2,3,4,5) is described in detail. The materials could be polymerized thermally, in the liquid state.",

author = "Eugen Barbu and John Tsibouklis",

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AU - Tsibouklis, John

PY - 1996/7/8

Y1 - 1996/7/8

N2 - A general method for the synthesis of pure samples of unsymmetrically disubstituted diacetylenes of the type CH3(CH2)nCCCCCH2OH (n=2,3,4,5) is described in detail. The materials could be polymerized thermally, in the liquid state.

AB - A general method for the synthesis of pure samples of unsymmetrically disubstituted diacetylenes of the type CH3(CH2)nCCCCCH2OH (n=2,3,4,5) is described in detail. The materials could be polymerized thermally, in the liquid state.

U2 - 10.1016/0040-4039(96)01025-8

DO - 10.1016/0040-4039(96)01025-8

M3 - Article

SN - 0040-4039

VL - 37

SP - 5023

EP - 5026

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 28

ER -

Unsymmetrically substituted aliphatic diacetylenes

Abstract

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