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Volumn 2002, Issue 8, 2002, Pages 91-111

Generation and cycloaddition of semi-stabilized 2-azaallyllithiums viaelectrocyclic ring-opening or cycloreversion reactions

Author keywords

2 azaallylanion; 2 azaallyllithium; Aziridine; Cycloreversion; Electrocyclic ring opening; Imidazolidine

Indexed keywords

2 (4 PENTENYL) 3 PHENYLAZIRIDINE; 4,5 DIPHENYL 3 (1 METHYLETHYL) 2 (4 METHYL 4 PENTENYL)IMIDAZOLIDINE; 4,5 DIPHENYL 3 (1 METHYLETHYL) 2 (4 PENTENYL)IMIDAZOLIDINE; AZIRIDINE DERIVATIVE; IMIDAZOLIDINE DERIVATIVE; N LITHIO 2,3 DIPHENYLAZIRIDINE; N LITHIOIMIDAZOLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 3242759731     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (25)
  • 1
    • 3242805673 scopus 로고    scopus 로고
    • note
    • Semi-stabilized 2-azaallyl anions are those bearing aryl groups. Non-stabilized versions bear only alkyl or hydrogen substituents, while the presence of groups such as esters, nitriles, and phosphonates denote stabilized 2-azaallyl anions.
  • 8
    • 3242809436 scopus 로고    scopus 로고
    • Royal Society of Chemistry, Cambridge, UK:; pp. Paper #060
    • An initial account of a portion of this work has appeared in an electronic proceeding: Pearson, W. H.; Walters, M. A.; Harter, W. G., in Electron. Conf. Heterocycl. Chem., [Proc.]; Royal Society of Chemistry, Cambridge, UK: 1996; pp. Paper #060 [http://www.ch.ic.ac.uk/ectoc/echet96/ papers/060/index.htm].
    • (1996) Electron. Conf. Heterocycl. Chem., [Proc.]
    • Pearson, W.H.1    Walters, M.A.2    Harter, W.G.3
  • 19
    • 3242744173 scopus 로고    scopus 로고
    • note
    • 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.