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Volumn , Issue 12, 2001, Pages 2221-2228

Stereoselective lateral functionalization of monosubstituted [2.2]paracyclophanes by directed ortho-metalation-homologous anionic fries rearrangement

Author keywords

Cyclophanes; Directed metalation; Fries rearrangement; Lateral functionalization; Stereoselective synthesis

Indexed keywords

4 HYDROXY N,N DIIDOPROPYL 5 TRIETHYLSILYL 2 [2.2]PARACYCLOPHANECARBOXAMIDE; N TERT BUTYL 4 [2.2]PARACYCLOPHANECARBOXAMIDE; PARACYCLOPHANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034971736     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200106)2001:12<2221::AID-EJOC2221>3.0.CO;2-3     Document Type: Article
Times cited : (25)

References (26)
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  • 10
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  • 11
    • 0004811174 scopus 로고    scopus 로고
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  • 12
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    • note
    • [2] However, the process was not optimized at that time.
  • 14
    • 0004769602 scopus 로고    scopus 로고
    • Dissertation, Technische Universität Braunschweig
    • For an alternate route to 4-oxazolinyl-[2.2]paracyclophane see Chr. Schulz, Dissertation, Technische Universität Braunschweig, 2000.
    • (2000)
    • Schulz, Chr.1
  • 19
    • 0002994828 scopus 로고
    • Lateral metalation is a well-established reaction in ortho-alkyl-substituted aromatics: R. D. Clark, R. Jahangir, Org. React. 1995, 47, 1-314.
    • (1995) Org. React. , vol.47 , pp. 1-314
    • Clark, R.D.1    Jahangir, R.2
  • 21
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.