Diastereoselective Titanium Enolate Aldol Reaction for the Total Synthesis of Epothilones
β Scribed by Koch, Guido; Loiseleur, Olivier; Fuentes, Daniel; Jantsch, Andrea; Altmann, Karl-Heinz
- Book ID
- 125546728
- Publisher
- American Chemical Society
- Year
- 2002
- Tongue
- English
- Weight
- 143 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1523-7060
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Aldol reactions of bidentate aldehydes and cis-1-arylsulfonamido-2-indanyl ester derived titanium enolates proceed with excellent syn-diastereoselectivities and good to excellent isolated yields.
## 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 βFull Textβ option. The original article is trackable v
## 1998 hydroxycarboxylic acids hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters P 0280 ## 01 -075 Ester Derived Titanium Enolate Aldol Reaction: Highly Diastereoselective Synthesis of syn-and anti-Aldols. -Titanium enolates derived from esters (I) undergo aldol rea