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Volumn 132, Issue 18, 2010, Pages 6412-6418

Tandem processes identified from reaction screening: Nucleophilic addition to aryl N -phosphinylimines employing La(III)-TFAA activation

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOTYPES; FRIEDEL-CRAFTS; NUCLEOPHILIC ADDITIONS; NUCLEOPHILIC REACTION; TANDEM PROCESS; TRIFLATES; TRIFLUOROACETIC ANHYDRIDES;

EID: 77952026636     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja100346w     Document Type: Article
Times cited : (33)

References (60)
  • 4
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    • For examples of imino-ene reactions, see
    • For examples of imino-ene reactions, see
  • 10
    • 77952084761 scopus 로고    scopus 로고
    • See Supporting Information for complete experimental details
    • See Supporting Information for complete experimental details.
  • 13
    • 77952073063 scopus 로고    scopus 로고
    • For recent examples of aza -Friedel-Crafts alkylations, see
    • For recent examples of aza -Friedel-Crafts alkylations, see
  • 19
    • 77952017729 scopus 로고    scopus 로고
    • For formation of trans -β-methylstyrene from cyclopropyl-benzene, see
    • For formation of trans -β-methylstyrene from cyclopropyl-benzene, see
  • 21
    • 77952016931 scopus 로고    scopus 로고
    • For aza-Prins reactions, see
    • For aza-Prins reactions, see
  • 32
    • 77952022920 scopus 로고    scopus 로고
    • For the formal [3 + 2] addition of alkenes to benzhydrol cations, see
    • For the formal [3 + 2] addition of alkenes to benzhydrol cations, see
  • 39
    • 77952076177 scopus 로고    scopus 로고
    • note
    • 3 afforded a 23% isolated yield of 46.
  • 40
    • 77952066015 scopus 로고    scopus 로고
    • Relative stereochemistry was determined by NMR and X-ray crystallographic analyses
    • Relative stereochemistry was determined by NMR and X-ray crystallographic analyses.
  • 51
    • 77952034191 scopus 로고    scopus 로고
    • note
    • 3/TFAA) did not lead to observable crossover indicating that the retro- aza -Prins process is likely not operative.
  • 52
    • 77952071767 scopus 로고    scopus 로고
    • For reviews of [4 + 3] cyclizations, see
    • For reviews of [4 + 3] cyclizations, see
  • 55
    • 77952039544 scopus 로고    scopus 로고
    • For stepwise addition of dienes to N -aryl imines, see
    • For stepwise addition of dienes to N -aryl imines, see
  • 59
    • 77952078603 scopus 로고    scopus 로고
    • For a review of privileged structures, see
    • For a review of privileged structures, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.