Advances in synthetic approach to and antifungal activity of triazoles

• Kumari Shalini,
• Nitin Kumar,
• Sushma Drabu and
• Pramod Kumar Sharma

Beilstein J. Org. Chem. 2011, 7, 668–677, doi:10.3762/bjoc.7.79

• nitrogen atoms. However, flash vacuum pyrolysis at 500 °C leads to loss of molecular nitrogen (N2) to produce aziridine. Certain triazoles are relatively easy to cleave by ring–chain tautomerism. Synthesis of triazoles Substituted 1,2,3-triazoles can be produced by the azide–alkyne Huisgen cycloaddition in

A biphasic oxidation of alcohols to aldehydes and ketones using a simplified packed- bed microreactor

• Andrew Bogdan and
• D. Tyler McQuade

Beilstein J. Org. Chem. 2009, 5, No. 17, doi:10.3762/bjoc.5.17

• catalysts functionalized with an acetylene moiety can be tethered to AO using a Huisgen cycloaddition [39]. Azide-functionalized AO resin (AO-N3, 2) was prepared by treating AO with sodium azide (Scheme 1) [41]. The coupling of 4-hydroxy-TEMPO 3 with propargyl bromide (4) using sodium hydride yielded the

Synthesis of 2-substituted 9-oxa-guanines {5-aminooxazolo[5,4-d]pyrimidin- 7(6H)-ones} and 9-oxa-2-thio- xanthines {5-mercaptooxazolo[5,4-d]pyrimidin- 7(6H)-ones}

• Subrata Mandal,
• Wen Tai Li,
• Yan Bai,
• Jon D. Robertus and
• Sean M. Kerwin

Beilstein J. Org. Chem. 2008, 4, No. 26, doi:10.3762/bjoc.4.26

• with benzyl azide or 2-morpholinoethyl azide in the presence of catalytic CuSO4 and sodium ascorbate to afford the triazoles 9 and 10, respectively, in good yield (Figure 5). The copper-catalyzed Huisgen cycloaddition of terminal alkynes and alkyl azides favors formation of the 1,4-triazole