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One-Pot Conversion of Trimethylsilyl Ethers into Urethanes Using Chlorosulfonyl Isocyanate: Application to the Synthesis of a Novel Neuromodulator Carisbamate
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  • One-Pot Conversion of Trimethylsilyl Ethers into Urethanes Using Chlorosulfonyl Isocyanate: Application to the Synthesis of a Novel Neuromodulator Carisbamate
  • One-Pot Conversion of Trimethylsilyl Ethers into Urethanes Using Chlorosulfonyl Isocyanate: Application to the Synthesis of a Novel Neuromodulator Carisbamate
저자명
Dong. Guang-Ri,Li. Qing-Ri,Woo. Seol-Hee,Kim. In-Su,Jung. Young-Hoon
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2008년|31권 11호|pp.1393-1398 (6 pages)
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대한약학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

This paper reports a novel synthetic method for the preparation of various urethanes and the application to the synthesis of carisbamate. The reaction of primary (2a, 2e and 2f) or secondary (2g-2i) trimethylsilyl ethers with chlorosulfonyl isocyanate afforded the corresponding urethanes in good yields without affecting the olefin moiety. However, in the case of secondary benzylic trimethylsilyl ether 2j, the corresponding urethane 3j was obtained in low yield. From the difference in reactivity between the primary and secondary benzylic trimethylsilyl ethers, the one-pot synthesis of carisbamate 1 from bis-trimethylsilyl ether 21 was achieved.