ChemInform Abstract: An Integrated Chemoenzymatic Synthesis of Enantiopure (-)-(1R,5S)- Cyclosarkomycin: A Sarkomycin Precursor.
β Scribed by L. ANDRAU; J. LEBRETON; P. VIAZZO; V. ALPHAND; R. FURSTOSS
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
An Integrated Chemoenzymatic Synthesis of Enantiopure (-)-(1R,5S)-Cyclosarkomycin: A Sarkomycin Precursor. -The presented five-step sequence to the known title precursor (V) of sarkomycin (VI) is synthesized in 21% overall yield, which is comparable to other procedures. By the use of a new culture medium the known transformation to the optically active lactone (II) is further optimized. The structure of the minor diastereomer (III) is determined by X-ray analysis.
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Chemoenzymatic Synthesis of (2R,5S)-and (2R,5R)-5-(1-Hydroxy-1methylethyl)-2-methyl-2-vinyltetrahydrofuran ('Linalool Oxide'): Preparative Application of a Highly Selective Bacterial Epoxide Hydrolase. -The synthesis of the title compounds (V) and (VI) is based on a chemoenzymatic kinetic resolutio
Application of the Stereoselective Diels-Alder Reaction of Enantiopure 2-Sulfinyl Dienes: Synthesis of (-)-(1S,5R)-Karahana Ether. -The natural karahana ether (VII) is synthesized for the first time by application of sulfinyl derivative (I) as chiral auxiliary in asymmetric Diels-Alder reaction and
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