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Volumn 10, Issue 10, 1971, Pages 743-744

The Arenology Principle

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84981915238     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.197107431     Document Type: Article
Times cited : (23)

References (18)
  • 1
    • 84981968109 scopus 로고    scopus 로고
    • Protophanes and Polyarenes, Part 4.‐ Part 3: [2].
  • 6
    • 0001274286 scopus 로고
    • Neuere Methoden der präparativen organischen Chemie IV Synthesen mit heterocyclischen Amiden (Azoliden)
    • (1962) Angewandte Chemie , vol.74 , pp. 407
    • Staab, H.A.1
  • 15
    • 84981936888 scopus 로고    scopus 로고
    • Strong Lewis acids presumably can be used for activation in several cases.
  • 16
    • 84981909200 scopus 로고    scopus 로고
    • This order is not intended to state that the two types of functional groups correspond best when the heteroatoms correspond.
  • 17
    • 84981933071 scopus 로고    scopus 로고
    • In the sense of column 3 of Table 2, i. e. not semiarenologous.
  • 18
    • 84981936941 scopus 로고    scopus 로고
    • The pyridine nucleus reacts with nucleophiles analogously to a carbonyl group with good negative leaving groups. Only with bad negative leaving groups (aldehydes, ketones) does the carbonyl group behave differently (addition instead of substitution).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.