Synlett 2006(3): 0481-0483  
DOI: 10.1055/s-2006-926237
LETTER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Alaremycin

Yong-Gang Wanga, Masaaki Wachib, Yuichi Kobayashi*a
a Department of Biomolecular Engineering, Tokyo Institute of Technology, B-52, Nagatsuta-cho 4259, Midori-ku, Yokohama 226-8501, Japan
Fax: +81(45)9245789; e-Mail: ykobayas@bio.titech.ac.jp;
b Department of Bioengineering, Tokyo Institute of Technology, J2-14, Nagatsuta-cho 4259, Midori-ku, Yokohama 226-8501, Japan
Further Information

Publication History

Received 1 November 2005
Publication Date:
06 February 2006 (online)

Abstract

Methyl 5-azido-4-oxohexanoate was synthesized from 5-hexenoic acid in six steps and converted to the title compound by NaReO4- and CF3SO3H-catalyzed reaction in Ac2O/CCl4 followed by hydrolysis of the methyl ester moiety.

9

Another sequence shown below produced (α-chloro)ethyl ketone i in low yield (Scheme [2] ).

10

Acid 6 is commercially available, but was conveniently prepared from cyclohexanone in 67% yield by oxidative ring cleavage with H2O2, FeSO4, and CuSO4. [11]

13

Although the original procedure [12] uses PEG-2000 as an additive, the reaction in H2O was found to be quite successful.