𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A stereocontrolled approach to (±)-nonactic acid

✍ Scribed by Yuedong Zhou; Qiongfeng Xu; Hongbin Zhai


Book ID
104095564
Publisher
Elsevier Science
Year
2008
Tongue
French
Weight
147 KB
Volume
49
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Racemic nonactic acid was efficiently constructed in a convergent, stereocontrolled fashion (7 steps, 27%). The present synthesis features a stereocontrolled 1,3-dione reduction with NaBH 4 /Et 2 B(OMe) and an acid-promoted stereospecific cyclization in the formation of 7.


📜 SIMILAR VOLUMES


ChemInform Abstract: Stereocontrolled Ap
✍ Hiroshi Nakagawa; Tsutomu Sugahara; Kunio Ogasawara 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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

A general and stereoselective approach t
✍ Gérard Mandville; Christian Girard; Robert Bloch 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 569 KB

A total synthesis of (+)-methyl nonactate from a chiral synthon obtained by enantioselective enzymatic transesterification is described. This new approach involves stereoselective reactions of aldolisation, reduction and intramolecular Michael addition and appears to be quite general since it could

ChemInform Abstract: A General and Stere
✍ G. MANDVILLE; C. GIRARD; R. BLOCH 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 2 views

A General and Stereoselective Approach to Nonactate Esters and Isomers: A Versatile Synthesis of (+)-Methyl Nonactate. -The title compound (XIII), which is a subunit of the macrotetrolide antibiotic nonactin, is stereoselectively synthesized from the chiral hydroxyacetate (I) in 11 steps and 6.4% o