Chiral Functionalization of 2(3H)-Thiazolone. New Route to Chiral Synthons for 2-Amino Thiols.
β Scribed by Hirokazu Isozumi; Shigeki Hoshimoto; Hirofumi Matsunaga; Takehisa Kunieda
- Book ID
- 101948360
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 158 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
For Abstract see ChemInform Abstract in Full Text.
π SIMILAR VOLUMES
## Abstract The heterospirocyclic __N__βmethylβ__N__βphenylβ5βoxaβ1βazaspiro[2.4]heptβ1βe nβ2βamine **(6**) and __N__β(5βoxaβ1βazaspiro[2.4]heptβ1βenβ2βyl)β(__S__)βproline methyl ester (**7**) were synthesized from the corresponding heterocyclic thiocarboxamides **12** and **10**, respectively, by
Enantioselective Synthesis of Benzylbutyrolactones from 5-Hydroxyfuran-2(5H)-one. New Chiral Synthons for Dibenzylbutyrolactone Lignans by a Chemoenzymatic Route. -Ongoing interest in lignan chemistry leads to the development of an efficient approach to the chiral acetate (R)-(III). In this proces
Binaphthyl derivatives 1-5, substituted in the 2-or 2,2Πpositions are used in palladium-catalyzed Suzuki coupling reactions. The mono-and bis-borylated coupling components 2, 4 and 5 can easily be prepared and purified, are air-stable and are therefore interesting starting materials for Suzuki coupl