Synthesis and Reactions of Oxazoles

Synthesis and Hetero-Michael Addition Re

Synthesis and Hetero-Michael Addition Reactions of 2-Alkynyl Oxazoles and Oxazolines.

✍ Peter Wipf; Thomas H. Graham 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 39 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

Synthesis and Hetero-Michael Addition Re

Synthesis and Hetero-Michael Addition Reactions of 2-Alkynyl Oxazoles and Oxazolines.

✍ Peter Wipf; Thomas H. Graham 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 34 KB

Tandem Multicomponent/Click Reactions: S

Tandem Multicomponent/Click Reactions: Synthesis of Functionalized Oxazoles and Tetrazoles from Acyl Cyanides.

✍ Isabelle F. Clemencon; Bruce Ganem 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 26 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Synthesis and Reaction of the First Oxaz

Synthesis and Reaction of the First Oxazol-4-ylboronates: Useful Reagents for the Preparation of Oxazole-Containing Biaryl Compounds.

✍ Hiroshi Araki; Tadashi Katoh; Munenori Inoue 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 23 KB

ChemInform Abstract: Synthesis and Fried

ChemInform Abstract: Synthesis and Friedlaender Reactions of 5-Amino-4-cyano-1,3-oxazoles.

✍ M. Carmo Carreiras; Ana Eleuterio; Catarina Dias; M. Alexandra Brito; Dora Brite 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Synthesis and React

ChemInform Abstract: Synthesis and Reactions of a Novel Furo[3,4-d]oxazole.

✍ Stephan Reck; Willy Friedrichsen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Synthesis and Reactions of a Novel Furo [3,4-d]oxazole. -The novel title compound (V), obtained by Rh-catalyzed decomposition of the diazo precursor, undergoes [4 + 2] cycloadditions with usual dienophiles. Density functional theoretical studies are in qualitative agreement with experimental data.