Stereoselective Synthesis of the Naturally Occurring 2-Pyranone Dodoneine

Stereoselective Syntheses of Naturally O

Stereoselective Syntheses of Naturally Occurring 5,6-Dihydropyran-2-ones

✍ J. Alberto Marco; Miguel Carda; Juan Murga; Eva Falomir 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 11 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.

Stereoselective Synthesis of the Core of

Stereoselective Synthesis of the Core of Naturally Occurring anti-HIV Isolitseane B.

✍ Paul Bremond; Elodie Girardeau; Yoann Coquerel; Jean Rodriguez 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 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, please click on HTML or PDF.

The Synthesis of Naturally Occurring ()-

The Synthesis of Naturally Occurring ()-Calyculin A

✍ Dr. Norihiko Tánimoto; Dr. Samuel W. Gerritz; Dr. Akiyoshi Sawabe; Dr. Takeshi N 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 355 KB 👁 2 views

Stereoselective Synthesis of Isomers of

Stereoselective Synthesis of Isomers of the Naturally Occurring 13-Hydroxy-2,4,9-tetracatrienoic Acid. Part 2.

✍ Antje Huefner; Christa Hoeller; Gottfried Reznicek 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 146 KB

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

Stereoselective Synthesis of the Natural

Stereoselective Synthesis of the Naturally Occurring Lactones (−)-Osmundalactone and (−)-Muricatacine Using Ring-Closing Metathesis

✍ Miguel Carda; Santiago Rodríguez; Florenci González; Encarnación Castillo; Alici 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 1 views

The stereoselective synthesis of the naturally occurring lactones osmundalactone (-)-1 and muricatacin (-)-2 is described. The key steps in each synthesis are the stereoselective addition of a Grignard reagent to a suitably protected αhydroxy aldehyde and a ring-closing metathesis.

Stereoselective Synthesis of the Natural

Stereoselective Synthesis of the Naturally Occurring Lactones(−)-Osmundalactone and (−)-Muricatacine Using Ring-Closing Metathesis

✍ Miguel Carda; Santiago Rodríguez; Florenci González; Encarnación Castillo; Alici 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 27 KB 👁 1 views

The structure of the metathesis catalyst 10 depicted in Scheme 2 on page 2650 is not correct; instead, it should read PhCHϭRuCl 2 (PCy 3 ) 2 (Cy ϭ cyclohexyl).