A Pentenyl Dianion Based Strategy for Convergent Synthesis of Ene-1,5-diols.
β Scribed by Adilah B. Bahadoor; Alec Flyer; Glenn C. Micalizio
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 29 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
A ready asymmetric synthesis of 3Π-oxathionucleosides has overall yield and considerable enantiomeric excesses. It represents a general synthetic path to prepare a wide range been accomplished in three main steps from benzoyloxyethanal. The synthesis is characterized by high of heterosubstituted sul
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## Abstract The [1,1β²βbiisoquinoline]β4,4β²βdiol (**4a**), which was obtained as hydrochloride **4a**β 2β HCl in two steps starting from the methoxymethyl (MOM)βprotected 1βchloroisoquinoline **8** (__Schemeβ 3__), opens access to further Oβfunctionalized biisoquinoline derivatives. Compound **4a**β 2β H