Thionation of β-lactams to β-thiolactams by silica-supported P2S5
摘要:
In this paper, an improved method for the thionation of -lactams is described. Using a solid-supported P2S5 reagent and heating under reflux conditions, -thiolactams were obtained in good to excellent yields. Also the reaction time reduced significantly compared with that achieved under the more conventional method using P2S5 alone. Furthermore, inexpensive and easily available starting materials simple reaction conditions and a simple purification process are some other advantages of this method.[GRAPHICS].
The Vilsmeier reagent: a useful and versatile reagent for the synthesis of 2-azetidinones
作者:Aliasghar Jarrahpour、Maaroof Zarei
DOI:10.1016/j.tet.2009.02.005
日期:2009.4
and oxalyl chloride or thionyl chloride, works as a versatile acid activator reagent for the direct [2+2] ketene–imine cycloaddition of substituted acetic acid and imines in one-pot synthesis under mild conditions. Monocyclic, spirocyclic and 3-electron-withdrawing group β-lactams were synthesized by this method and optimization of conditions were performed.
Utilization of DMF–PhCOCl Adduct as an Acid Activator in a New and Convenient Method for Preparation of β-Lactams
作者:Maaroof Zarei
DOI:10.1246/bcsj.20110323
日期:2012.3.15
An efficient one-potsynthesis of β-lactams by the reaction of imines with acetic acid derivatives in the presence of DMF and benzoyl chloride adduct, a cheap reagent, has been described. Optimizat...
Synthesis of Novel N-(4-Ethoxyphenyl) Azetidin-2-ones and Their Oxidative N-Deprotection by Ceric Ammonium Nitrate
作者:Aliasghar Jarrahpour、Maaroof Zarei
DOI:10.3390/12102364
日期:——
It is shown that the N-(p-ethoxyphenyl) group on beta-lactams can be oxidatively removed by ceric ammonium nitrate in good yield. Fourteen newN-(p-ethoxyphenyl)-2-azetidinones 8a-n were synthesized through standard [2+2] ketene-imine cycloadditions (Staudinger reaction). Treatment of these compounds with ceric ammonium nitrate yielded the N-dearylated 2-azetidinones 9a-n in good to excellent yields
From Solution-Phase to ‘On-Column’ N-Dearylation of β-Lactams by Silica-Supported Ceric Ammonium Nitrate (CAN-SiO<sub>2</sub>)
作者:Aliasghar Jarrahpour、Maaroof Zarei
DOI:10.1055/s-2008-1032051
日期:2008.2
It has been shown that N-(4-methoxy or 4-ethoxyphenyl) groups can be oxidatively removed by silica gel supported ceric ammonium nitrate (CAN-SiO2) under mild conditions in solution and on column. The yields in these two methods were good to excellent and purification of products is simpler than the general method by CAN. Especially the ‘on-column’ reaction is mild, easy, efficient, and cheap. The lower mobility of CAN-SiO2 makes it safer to handle.
The Vilsmeier reagent as an efficient acid activator for the synthesis of β-lactams
作者:Aliasghar Jarrahpour、Maaroof Zarei
DOI:10.1016/j.tetlet.2007.10.012
日期:2007.12
The Vilsmeier reagent (chloromethylenedimethylammonium chloride) has been used as an efficient and cheap acid activator for the one-step Staudinger reaction of substituted acetic acids and imines under mild conditions. This reaction is clean and the by-products are DMF and triethylamine hydrochloride which were removed by simple aqueous work-up. (c) 2007 Published by Elsevier Ltd.