Regio- and stereoselective Hydrosilylation of Terminal Alkynes Using Grubbs′ First-Generation Olefin-Metathesis Catalyst.

An Efficient Ring-Closing Metathesis Rea

An Efficient Ring-Closing Metathesis Reaction of Geminally Disubstituted Olefins Using First Generation Grubbs′ Catalyst: Enantiospecific Synthesis of Pacifigorgianes.

✍ A. Srikrishna; Dattatraya H. Dethe 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 126 KB

New Approach to the Synthesis of Macrocy

New Approach to the Synthesis of Macrocyclic Tetralactones via Ring-Closing Metathesis Using Grubbs′ First-Generation Catalyst.

✍ Sengodagounder Muthusamy; Boopathy Gnanaprakasam; Eringathodi Suresh 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 23 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.

Highly Chemo- and Stereoselective Interm

Highly Chemo- and Stereoselective Intermolecular Coupling of Diazoacetates To Give cis-Olefins by Using Grubbs Second-Generation Catalyst

✍ David M. Hodgson; Deepshikha Angrish 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 214 KB

Highly Chemo- and Stereoselective Interm

Highly Chemo- and Stereoselective Intermolecular Coupling of Diazoacetates to Give cis-Olefins by Using Grubbs′ Second-Generation Catalyst.

✍ David M. Hodgson; Deepshikha Angrish 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 36 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.