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Volumn 72, Issue 21, 2007, Pages 8142-8145

Practical and robust method for regio- and stereoselective preparation of (E)-ketene tert-butyl TMS acetals and β-ketoester-derived tert-butyl (1Z,3E)-1,3-bis(TMS)dienol ethers

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTYL METHYL ETHER; TERT-BUTYL ESTERS;

EID: 35348865523     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701456t     Document Type: Article
Times cited : (29)

References (68)
  • 2
    • 35348849775 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
    • (b) Gennari, C. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 2, pp 630-657.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 630-657
    • Gennari, C.1
  • 30
    • 34247266658 scopus 로고    scopus 로고
    • CPME was recently launched by the Zeon group and applied the useful ether solvent in the place of THF, dioxolane, DME, etc. Watanabe, K, Yamagiwa, N, Torisawa, Y. Org. Process Res. Dev. 2007, 11, 251. Appropriate bp 106°C, low solubility in water high separation property, low formation of peroxides, relative stability under acidic and basic conditions, formation of azeotropes with water, a narrow explosion range
    • CPME was recently launched by the Zeon group and applied the useful ether solvent in the place of THF, dioxolane, DME, etc. Watanabe, K.; Yamagiwa, N.; Torisawa, Y. Org. Process Res. Dev. 2007, 11, 251. Appropriate bp 106°C, low solubility in water (high separation property), low formation of peroxides, relative stability under acidic and basic conditions, formation of azeotropes with water, a narrow explosion range.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.