๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

ChemInform Abstract: Total Synthesis of Epothilone A.

โœ Scribed by Rama M. Hindupur; Bijoy Panicker; Muralikrishna Valluri; Mitchell A. Avery

Publisher
John Wiley and Sons
Year
2010
Weight
23 KB
Volume
33
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of (-)-Epothilone A.
โœ D. SCHINZER; A. LIMBERG; A. BAUER; O. M. BOEHM; M. CORDES ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 30 KB ๐Ÿ‘ 2 views

Total Synthesis of (-)-Epothilone A. -A key step in the synthesis of the title antitumor natural product is the highly stereoselective aldol reaction of the optically active building blocks (I) and (II). Esterification of the product (IV) with the subunit (V) leads to the stereochemically homogeneou

ChemInform Abstract: Total Synthesis of
ChemInform Abstract: Total Synthesis of Epothilone A: The Olefin Metathesis Approach.
โœ Z. YANG; Y. HE; D. VOURLOUMIS; H. VALLBERG; K. C. NICOLAOU ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 29 KB ๐Ÿ‘ 1 views

Total Synthesis of Epothilone A: The Olefin Metathesis Approach. -Starting with the three building blocks (I)-(III) the coupling product (IV) is obtained. It is used for olefin metathesis as the key step in the synthesis of the title compound (VI). -(YANG, Z.;