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Volumn 76, Issue 5, 2011, Pages 1499-1502

Synthesis of tetrahydrofurans by cyclization of homoallylic alcohols with iodine/iodine(III)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYTIC AMOUNTS; CYCLOFUNCTIONALIZATION; ELECTROPHILIC ADDITIONS; HOMOALLYLIC ALCOHOL; RING EXPANSION; TETRA-HYDROFURAN; TETRAHYDROFURANS;

EID: 79952168202     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo102413u     Document Type: Article
Times cited : (25)

References (57)
  • 43
    • 79952130731 scopus 로고    scopus 로고
    • Conditions tested were the following: 1 equiv of DIB, MeOH, rt, 30 min
    • Conditions tested were the following: 1 equiv of DIB, MeOH, rt, 30 min
  • 44
    • 79952158379 scopus 로고    scopus 로고
    • 1 equiv of DIB, MeCN, rt (3 d), reflux (7 h)
    • 1 equiv of DIB, MeCN, rt (3 d), reflux (7 h)
  • 45
    • 79952153252 scopus 로고    scopus 로고
    • 1 equiv of DIB, 3.0 equiv of KOH, MeOH, rt, 4 d.
    • 1 equiv of DIB, 3.0 equiv of KOH, MeOH, rt, 4 d.
  • 51
    • 0038445018 scopus 로고    scopus 로고
    • Reactivities, Properties and Structures, in Hypervalent Iodine Chemistry: Modern Developments in Organic Synthesis
    • It was estimated that the I(III) is a better leaving group than I by a factor of 10 (13, 14). For a discussion, see:,-68
    • It was estimated that the I(III) is a better leaving group than I by a factor of 10 (13, 14). For a discussion, see: Ochiai, M. Reactivities, Properties and Structures, in Hypervalent Iodine Chemistry: Modern Developments in Organic Synthesis Top. Curr. Chem. 2003, 5-68
    • (2003) Top. Curr. Chem. , pp. 5
    • Ochiai, M.1
  • 57
    • 79952145064 scopus 로고    scopus 로고
    • See the Supporting Information for additional conditions.
    • See the Supporting Information for additional conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.