ChemInform Abstract: Synthesis of an Enantiomerically Pure Carbocyclic DNA Abasic Site Analogue.
β Scribed by Martial Thomas; Bertrand Castaing; Jean-Louis Fourrey; Charles Zelwer
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Synthesis of Enantiomerically Pure Carbocyclic Ξ±-L-Isomeric Homonucleosides. -The synthesis of hitherto unknown carbocyclic 2',3'-dideoxyhomonucleosides (X)-(XIII) starting from the known chiral lactone (I) is accomplished. The transformation of the (R)-hydroxy group in derivative (IV) to the
## 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 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
Synthesis of an Enantiomerically Pure Serine-Derived Thiazole. -The bulky trityl group is shown to be the N-protecting group of choice in the synthesis of serine-derived thiazole amino acids. The trityl-group serves as a protecting group in the key-step, the conversion of thioamide (V) to the thiaz