(268)Alkynol Synthesis II Propargyl Alcohol

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Addition of Ethyl Alcohol to Triethyl Propargyl Ammonium Bromide

Rearrangement of propargyl amine salt, in the presence of a base was studied and it was concluded that this occurs through an allenic intermediate.

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Propargyl Claisen rearrangement: allene synthesis and beyond.

The propargyl Claisen rearrangement is a known protocol to gain access to functionalized allenes through the [3,3]-sigmatropic transformation of propargyl vinyl ethers. The correct use of appropriate propargyl vinyl ethers as starting materials coupled with suitable reaction conditions can aid in the development of new domino methodologies in which the allenes are valuable intermediates in rout...

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Synthesis of Triethyl Propargyl Ammonium Bromide from Triethyl Amine With Propargyl Bromide

The reaction between trimethylamine with propargyl bromide was studied and the structure of triethyl propargyl ammonium bromide was illustrated by 1HNMR, IR, and Mass spectra.

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addition of ethyl alcohol to triethyl propargyl ammonium bromide

rearrangement of propargyl amine salt, in the presence of a base was studied and it was concluded that this occurs through an allenic intermediate.

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A striking exception to the chelate model for acyclic diastereocontrol: efficient access to a versatile propargyl alcohol for chemical synthesis.

The four-step, asymmetric synthesis of a chiral propargyl alcohol 1 from (R)-pantolactone is described. A key feature of the synthesis is a diastereoselective acetylide addition to a chiral alpha-alkoxy-aldehyde 7, in which unusual Felkin selectivity is observed, despite the potential for chelation control. Crystalline propargyl alcohol 1 is valuable for complex molecule synthesis, and is easy ...

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ژورنال

عنوان ژورنال: The Journal of the Society of Chemical Industry, Japan

سال: 1952

ISSN: 0023-2734,2185-0860

DOI: 10.1246/nikkashi1898.55.567