Solid phase synthesis of hydantoin library using a novel cyclization and traceless cleavage step
โ Scribed by Sang Woong Kim; Sang Youl Ahn; Jong Sung Koh; Jin Ho Lee; Seonggu Ro; Hae Yeon Cho
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 165 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The variety of N, N-disubstituted hydantoin libraries were constructed using derivatives of amino acids, aromatic aldehydes, and isocyanates. The cyclization step of hydantoin was a novel, fast, and clean reaction and completed within five minutes to I hour with neat diisopropylamine. All library compounds were obtained in excellent yield with high purity even after 5 steps.
๐ SIMILAR VOLUMES
N-Methyloctadepsipeptides attached to an oxime resin were cyclized by heating them in refluxing ethyl acetate for 2 days to give cyclooctadepsipeptide PFI022A analogs.