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Volumn , Issue 4, 1999, Pages 444-446

Stereoselectivity in amidyl radical cyclisations: Alkyl mode cyclisations

Author keywords

Amidyl radicals; Cyclisation; Hydroxamic acid derivatives; Pyrrolidinones; Stereochemistry

Indexed keywords

HYDROXAMIC ACID DERIVATIVE; RADICAL;

EID: 0032895121     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2640     Document Type: Article
Times cited : (26)

References (26)
  • 15
    • 85069246121 scopus 로고    scopus 로고
    • note
    • Yield 53% is given for an inseparable mixture of cyclised compounds 7e, 8e and reduced compound 9e.
  • 16
    • 85069254977 scopus 로고    scopus 로고
    • note
    • The best approach to remove excess tin residues before chromatography was to partition the crude reaction mixture between cyclohexane and acetonitrile and then evaporate the acetonitrile layer to furnish purified cyclised materials.
  • 19
    • 85069254738 scopus 로고    scopus 로고
    • note
    • 3) 169.5, 135.8, 128.7, 128.3, 126.4, 53.6, 53.0, 41.6, 30.7, 28.9, 21.7, 18.8
  • 21
  • 22
    • 85069255412 scopus 로고    scopus 로고
    • note
    • 25,26 gradient corrections. Basis sets were STO triple-ζ + polarisation on all atoms.
  • 24
    • 0004314111 scopus 로고    scopus 로고
    • Theoretical Chemistry, Vrije Universiteit, Amsterdam
    • ADF version 2.3.0, Theoretical Chemistry, Vrije Universiteit, Amsterdam, 1997.
    • (1997) ADF Version 2.3.0


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.