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Volumn 40, Issue 11, 1999, Pages 2145-2148

Efficient synthesis of 2,3-trans-tetrahydropyrans and oxepanes: Rearrangement-ring expansion of cyclic ethers having a chloromethanesulfonate

Author keywords

Oxepanes; Rearrangements; Stereocontrol; Tetrahydropyrans

Indexed keywords

METHYL CHLORIDE; OXEPANE DERIVATIVE; TETRAHYDROPYRAN DERIVATIVE;

EID: 0033548555     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00134-3     Document Type: Article
Times cited : (38)

References (19)
  • 14
    • 0013579787 scopus 로고    scopus 로고
    • 2 (Tf)
    • 2 (Tf).
  • 16
    • 0013631621 scopus 로고    scopus 로고
    • 2O (50 °C, 6 h, 69%; reflux, 2 h, 88%)
    • 2O (50 °C, 6 h, 69%; reflux, 2 h, 88%).
  • 17
    • 0013608122 scopus 로고    scopus 로고
    • 3 2 equiv, 9h, 63% (4a: 40%, 4c: 23%
    • 3 (2 equiv, 9h, 63% (4a: 40%, 4c: 23%).
  • 18
    • 0013577721 scopus 로고    scopus 로고
    • The 1,3-diaxial repulsion by the substituents would cause an acceleration of this rearrangement
    • The 1,3-diaxial repulsion by the substituents would cause an acceleration of this rearrangement.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.