Over the last several decades, numerous heterocycles have emerged as useful tools (precursors, reagents, chiral auxiliaries) in new methodologies for organic synthesis.2 In that context, the five-membered heterocycle 1,3-thiazole attained considerable popularity by virtue of its stability under a wide range of reaction conditions, as well as its facile conversion into the formyl group by a very efficient three-step one-pot procedure. The widespread use of the thiazole ring as masked formyl group led to the formulation of a general synthetic strategy that we have referred to as the “Thiazole-Aldehyde Synthesis”.

Discussion Addendum for: Diastereoselective homologation of D-(R)-glyceraldehyde acetonide using 2-(trimethylsilyl)thiazole: 2-O-benzyl-3,4-isopropylidene-D-erythrose

DONDONI, Alessandro;MARRA, Alberto
2012

Abstract

Over the last several decades, numerous heterocycles have emerged as useful tools (precursors, reagents, chiral auxiliaries) in new methodologies for organic synthesis.2 In that context, the five-membered heterocycle 1,3-thiazole attained considerable popularity by virtue of its stability under a wide range of reaction conditions, as well as its facile conversion into the formyl group by a very efficient three-step one-pot procedure. The widespread use of the thiazole ring as masked formyl group led to the formulation of a general synthetic strategy that we have referred to as the “Thiazole-Aldehyde Synthesis”.
2012
Dondoni, Alessandro; Marra, Alberto
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1664479
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