메뉴 건너뛰기




Volumn 13, Issue 8, 2011, Pages 1996-1999

Cyclopropane-Aldehyde annulations at quaternary donor sites: Stereoselective access to highly substituted tetrahydrofurans

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; CYCLOPROPANE; CYCLOPROPANE DERIVATIVE; FURAN DERIVATIVE;

EID: 79955453983     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200395e     Document Type: Article
Times cited : (93)

References (29)
  • 22
    • 79955367382 scopus 로고    scopus 로고
    • The reaction showed broad solvent and Lewis acid tolerance, but the high reactivity observed with Sn(OTf)2 and 1,2-DCE led us to to use this combination for most substrates
    • The reaction showed broad solvent and Lewis acid tolerance, but the high reactivity observed with Sn(OTf)2 and 1,2-DCE led us to to use this combination for most substrates.
  • 23
    • 79955414364 scopus 로고    scopus 로고
    • Significant aldehyde decomposition was observed when isobutyraldehyde was used in combination with slower-reacting cyclopropanes (4d, 4e, and 4 g)
    • Significant aldehyde decomposition was observed when isobutyraldehyde was used in combination with slower-reacting cyclopropanes (4d, 4e, and 4 g).
  • 24
    • 79955401443 scopus 로고    scopus 로고
    • For examples of Lewis acid catalyzed THF ring opening, see
    • For examples of Lewis acid catalyzed THF ring opening, see.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.