Practical synthesis of α-aminoalkyl-α′-chloromethylketone derivatives. Part 2: Chloromethylation of N-imine-protected amino acid esters
✍ Scribed by Tomoyuki Onishi; Takashi Nakano; Naoko Hirose; Masakazu Nakazawa; Kunisuke Izawa
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 87 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Chloromethylation of N-imine-protected amino acid esters followed by acid hydrolysis gave a-aminoalkyl-a%chloromethylketone as a HCl salt form in good yield without racemization. The amino group was conveniently protected with carbamate protecting reagents to give various useful intermediates for the protease inhibitors.
📜 SIMILAR VOLUMES
Moc; Methoxycarbonyloxy group 3 1) TMSCl, n BuLi 2) BrCH 2 Cl, n BuLi 3 steps, 76% 3) H +
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