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Volumn 46, Issue 4, 2005, Pages 599-602

The first example of magnesium carbenoid 1,3-CH insertion reaction: A novel method for synthesis of cyclopropanes from 1-chloroalkyl phenyl sulfoxides in high yields

Author keywords

C H insertion; Cyclopropane; Magnesium carbenoid; Sulfoxide; Sulfoxide magnesium exchange

Indexed keywords

BENZENE DERIVATIVE; CARBENOID; CYCLOPROPANE DERIVATIVE; MAGNESIUM DERIVATIVE; SULFOXIDE;

EID: 11144302018     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.11.146     Document Type: Article
Times cited : (27)

References (36)
  • 1
    • 0004050551 scopus 로고
    • Academic New York
    • The monographs concerning chemistry of carbenes and carbenoids: W. Kirmse Carbene Chemistry 1971 Academic New York
    • (1971) Carbene Chemistry
    • Kirmse, W.1
  • 31
    • 11144343245 scopus 로고    scopus 로고
    • note
    • 4 to give the desired 8 in high overall yield
  • 32
    • 84860065401 scopus 로고    scopus 로고
    • 1a pp 209-266
    • 1a pp 209-266
  • 33
    • 11144332455 scopus 로고    scopus 로고
    • note
    • 3P to give mono sulfide, which was oxidized with m-chloroperbenzoic acid to give a sulfoxide having a hydroxyl group. The hydroxyl group was protected with dihydropyrane and finally the THP-protected sulfoxide was chlorinated with NCS in THF to give 14 in good yield. The 1-chloroalkyl phenyl sulfoxides 16 and 18 were synthesized from 14
  • 34
    • 11144298636 scopus 로고    scopus 로고
    • note
    • 2: M, 170.1307. Found: m/z 170.1308


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.