ChemInform Abstract: Formal Synthesis of (-)-Neopeltolide Featuring a Highly Stereoselective Oxocarbenium Formation/Reduction Sequence.
β Scribed by Dionicio Martinez-Solorio; Michael P. Jennings
- Book ID
- 102056379
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
A Highly Stereoselective Ξ²-(1β4)-Glycosidic Bond Formation by Reductive Cleavage of Cyclic Orthoesters. -Reduction of the orthoester (I) under the conditions shown provides the desired glycoside (II) with high Ξ²-selectivity. Application of a LiAlH4/AlCl3 reagent to the glycosidic spiro-orthoesters
## 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
## 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