The Burgess reagent is used to convert secondary and tertiary alcohols with an adjacent proton into alkenes. Dehydration of primary alcohols does not work well. The reagent is soluble in …

Mar 27, 2025 · Burgess Reagent Mechanism: The mechanism involves a stereospecific syn-elimination via ion-pair formation from the intermediate sulfamate ester (comparable to the …

May 3, 2016 · Burgess reagent was also utilized to promote several other transformations of great synthetic values in medicinal chemistry. In this Atlanchim letter, we will present a brief …

The Burgess reagent is a commercially available compound that has historically found utility as a dehydrating agent. The reagent may also be used to oxidize primary and secondary alcohols …

3 days ago · The Burgess reagent, a zwitterionic species known for its mild dehydrating capabilities, has emerged as a versatile tool in organic synthesis. These reagents are known …

Jan 29, 2021 · The Burgess reagent [methyl N-(triethylammoniumsulfonyl)carbamate], a neutral, white crystalline solid, is efficient at generating olefins from secondary and tertiary alcohols …

Mar 1, 2009 · An efficient chemoselective method for the preparation of nitriles from primary amides is described which utilizes methyl (car☐ysulfamoyl)triethylammonium hydroxide inner …

The Burgess reagent or Methyl N-(triethylammoniumsulphonyl)carbamate is a mild and selective dehydrating reagent often used in organic chemistry [1]. It is used to convert any alcohol with …

Oct 29, 2004 · This article delineates the power of these new reaction manifolds and demonstrates how the use of novel Burgess-type reagents extends the scope of these …

The Burgess reagent is a carbamate and used for the dehydration of various sec- and tert- alcohols to get the corresponding olefins. Moreover, it also found applications in numerous …