## Abstract An efficient and reliable multiโstep synthesis of 251 natural productโlike [5.5]โspiroketals on solid supports has been developed. As central key step, a double intramolecular heteroโMichael (DIHMA) reaction to alkynones was applied. The sequence allows for introduction of numerous subs
Solid-Phase Synthesis of 2-Amino-5-sulfanylthiazoles
โ Scribed by Marie Grimstrup; Florencio Zaragoza
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 148 KB
- Volume
- 2002
- Category
- Article
- ISSN
- 1434-193X
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โฆ Synopsis
A solid-phase synthesis that provides easy access to 2-amino-5-sulfanylthiazoles with variable substituents at C-2, C-4, and C-5 has been developed. The key step of this synthesis is a new C-sulfanylation of resin-bound 2-aminothiazoles by mixtures of various sulfur-containing building blocks and iodine. The resulting 2-amino-5-sulfanylthiazoles were obtained in high purities and yields after cleavage from the
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