메뉴 건너뛰기




Volumn 2015, Issue 18, 2015, Pages 3899-3904

Vicinal Functionalization of N‐Alkoxyenamines: Tandem Umpolung Phenylation–Nucleophilic Addition Reaction Sequence

Author keywords

Aldehydes; Alkoxyamines; En amines; Imines; Nucleophilic addition; Umpolung

Indexed keywords


EID: 85027950819     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201500308     Document Type: Article
Times cited : (9)

References (59)
  • 1
    • 85128591125 scopus 로고    scopus 로고
    • For reviews on enamine chemistry, see:
    • For reviews on enamine chemistry, see:.
  • 5
    • 85128598033 scopus 로고    scopus 로고
    • For reviews on enamide chemistry, see:
    • For reviews on enamide chemistry, see:.
  • 8
    • 84859101188 scopus 로고    scopus 로고
    • Dake, G.R., Synlett 23 (2012), 814–824.
    • (2012) Synlett , vol.23 , pp. 814-824
    • Dake, G.R.1
  • 13
    • 85128630090 scopus 로고    scopus 로고
    • Selected recent examples for vicinal functionalization of enamides:
    • Selected recent examples for vicinal functionalization of enamides:.
  • 19
    • 85128621667 scopus 로고    scopus 로고
    • Selected examples of intermolecular reactions:
    • Selected examples of intermolecular reactions:.
  • 29
    • 85128611612 scopus 로고    scopus 로고
    • PdII‐assisted intermolecular dialkylation and alkylation/acylation:
    • PdII‐assisted intermolecular dialkylation and alkylation/acylation:.
  • 32
    • 85128684167 scopus 로고    scopus 로고
    • Transition‐metal‐catalyzed cyclization:
    • Transition‐metal‐catalyzed cyclization:.
  • 38
    • 85128642658 scopus 로고    scopus 로고
    • .
  • 43
    • 85128619621 scopus 로고    scopus 로고
    • .
  • 46
    • 85128660011 scopus 로고    scopus 로고
    • .
  • 50
    • 85128600726 scopus 로고    scopus 로고
    • Selected recent examples of cycloaddition reactions utilizing enamines:
    • Selected recent examples of cycloaddition reactions utilizing enamines:.
  • 54
    • 85128595611 scopus 로고    scopus 로고
    • .
  • 58
    • 85128591376 scopus 로고    scopus 로고
    • In the umpolung β‐phenylation of N‐alkoxyenamine, the use of 2‐methylpropanal as α‐branched aldehyde led to the α‐phenylated aldehyde in 46 % yield.
    • In the umpolung β‐phenylation of N‐alkoxyenamine, the use of 2‐methylpropanal as α‐branched aldehyde led to the α‐phenylated aldehyde in 46 % yield.
  • 59
    • 85128682339 scopus 로고    scopus 로고
    • The relative configuration of threo‐7e (major diastereomer) was determined by converting threo‐7e into authentic cis‐15 (see the Supporting Information).
    • The relative configuration of threo‐7e (major diastereomer) was determined by converting threo‐7e into authentic cis‐15 (see the Supporting Information).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.