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- W2046328051 abstract "Oxalyl chloride is a very versatile reagent extensively used by organic chemists. One of its most common uses is in oxidation of alcohols to aldehydes and ketones named Swern oxidation. [1-5] However, this reagent can efficiently be applied in many other reactions such as 1,1-cycloadditions with 1,4-dilithio-1,3-dienes or zirconacyclopentadienes, [6] cyclization of 1,3-bis(trimethylsilyloxy) alk-1-enes to isoeletronic acids, [7] preparation of phenyl isocyanates from anilines, [8] bicyclization of biaryl acetamides, [9] dehydration of formamides to afford nitriles, [10] and cyclization of 1,1-bis(trimethylsilyloxy) ketene acetals to give 3-hydroxymaleic anhydrides. [11]" @default.
- W2046328051 created "2016-06-24" @default.
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- W2046328051 date "2007-04-01" @default.
- W2046328051 modified "2023-09-27" @default.
- W2046328051 title "Oxalyl Chloride: A Versatile Reagent in Organic Synthesis" @default.
- W2046328051 doi "https://doi.org/10.1055/s-2007-977431" @default.
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