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Volumn , Issue 12, 1997, Pages 1467-1474

Hetero Diels-Alder reactions of 2-chloro-1-nitroso-1-phenylethene: Preparation of novel 4-chloro-substituted 1,2-oxazines and subsequent reactions

Author keywords

1,2 Oxazine; Cis dihydroxylation; Hetero Diels Alder reaction; Hydrogenolysis; Silyl enol ether

Indexed keywords

1,2 OXAZINE DERIVATIVE; 2 CHLORO 1 NITROSO 1 PHENYLETHENE; OXAZINE DERIVATIVE; OXIME DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0031450822     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-1373     Document Type: Article
Times cited : (31)

References (63)
  • 35
    • 34548001862 scopus 로고    scopus 로고
    • Dissertation, Technische Universität Dresden
    • Angermann, J. Dissertation, Technische Universität Dresden, 1997.
    • (1997)
    • Angermann, J.1
  • 39
    • 34548000968 scopus 로고    scopus 로고
    • note
    • 3 failed. Only oligo- or polymeric products were observed.
  • 41
  • 44
    • 34548000022 scopus 로고
    • Dissertation, Technische Hochschule Darmstadt
    • Arnold, T. Dissertation, Technische Hochschule Darmstadt, 1992.
    • (1992)
    • Arnold, T.1
  • 47
    • 34548001621 scopus 로고    scopus 로고
    • note
    • A similar reaction of ethyl vinyl ether (4) with trichloro-N-hydroxyacetimidoyl chloride leading to O-(1-ethoxyethyl)-α-chloro-choral oxime was described by Kresze, Viehe et al., see ref. 16.
  • 57
    • 34548001921 scopus 로고
    • Dissertation, Technische Hochschule Darmstadt
    • It should be noted that reduction of 4-azido-5,6-dihydro-4H-1,2-oxazine 25 (cis:trans = 95:5) proceeded under standard conditions as expected. It gave 4-phenylbutane-1,3-diamine as the major product (58 % yield) and as a minor component was formed 3-amino-2-phenylpyrrolidine in 29 % yield as a mixture of two diastereomers (63:37): Paulini, K. Dissertation, Technische Hochschule Darmstadt, 1993.
    • (1993)
    • Paulini, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.