메뉴 건너뛰기




Volumn 346, Issue 7, 2004, Pages 713-716

Fluoride ion-promoted α-ketol rearrangement during unmasking of silyl-protected medium-ring dihydroxy ketones

Author keywords

ketols; Desilylation; Fluoride ion; Medium sized rings; MM3 calculations; Rearrangement

Indexed keywords

BASE; CARBONYL DERIVATIVE; FLUORIDE; HEPTANE DERIVATIVE; HYDROXYL GROUP; KETOL; KETONE DERIVATIVE; OCTANE; OXYGEN; SILICON;

EID: 4143069092     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200404002     Document Type: Article
Times cited : (6)

References (19)
  • 12
    • 0344148449 scopus 로고    scopus 로고
    • and relevant references cited therein
    • L. A. Paquette, P. C. Lobben, J. Org. Chem. 1998, 63, 5604 and relevant references cited therein.
    • (1998) J. Org. Chem. , vol.63 , pp. 5604
    • Paquette, L.A.1    Lobben, P.C.2
  • 18
    • 0002202998 scopus 로고
    • It is well recognized that anionicaly accelerated rearrangements are capable of proceeding at significantly lower temperatures: a) S. R. Wilson, Org. React. 1993, 43, 93; b) L. A. Paquette, Tetrahedron 1997, 53, 7403.
    • (1993) Org. React. , vol.43 , pp. 93
    • Wilson, S.R.1
  • 19
    • 4143067542 scopus 로고    scopus 로고
    • It is well recognized that anionicaly accelerated rearrangements are capable of proceeding at significantly lower temperatures: a) S. R. Wilson, Org. React. 1993, 43, 93; b) L. A. Paquette, Tetrahedron 1997, 53, 7403.
    • (1997) Tetrahedron , vol.53 , pp. 7403
    • Paquette, L.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.