ChemInform Abstract: A Metal-Mediated Diastereoselective Synthesis of Precursors to the Aphid Pigment Derivatives.
β Scribed by R. G. F. GILES; C. A. JOLL; M. V. SARGENT; D. M. G. TILBROOK
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Oxazaphosphorinane Precursors to the Diastereoselective Synthesis of DNA Phosphorothioates. -The chiral phosphorothioate (VIII) is diastereoselectively synthesized from the oxazaphosphorinane (VII) containing xylose as chiral auxiliary. In contrast, the cholesterol and camphor derivatives (III) and
Precursor to 25-Hydroxyvitamin D3. -The target vitamin D precursor (X) is synthesized in six steps with 31% overall yield. -(MICHALAK, K.;
## 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
Diastereoselective SmI 2 -Mediated Cascade Radical Cyclizations of Methylenecyclopropane Derivatives -A Synthesis of Paeonilactone B. -Using the title cascade reaction from (VII) to (IX) as key step the natural product paeonilactone B (XIV) is synthesized in an efficient manner. The relative stereoc
## 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 of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v