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Volumn 64, Issue 49, 2008, Pages 11086-11095

Investigation of oxacycle formation by base-promoted endo-mode ring-closing reaction of allenes

Author keywords

Allenes; endo Mode ring closure; Oxacycles; Tandem reaction

Indexed keywords

2 [1 (BENZYLOXY)ETHYLIDENE] 4 BUTANOLIDE; 2 [1 (BENZYLOXY)ETHYLIDENE] 5 PENTANOLIDE; ALLENE DERIVATIVE; BENZYL 2 METHYL 4,5 DIHYDROFURAN 3 CARBOXYLATE; BENZYL 2 METHYL 4,5,6,7 TETRAHYDROOXEPIN 3 CARBOXYLATE; BENZYL 4 HYDROXY 2 VINYLIDENEBUTANOATE; BENZYL 5 HYDROXY 2 VINYLIDENEPENTANOATE; BENZYL 6 HYDROXY 2 VINYLIDENEHEXANOATE; BENZYL 7 HYDROXY 2 VINYLIDENEHEPTANOATE; BENZYL 8 METHYL 3,4,5,6 TETRAHYDRO 2H OXOCIN 7 CARBOXYLATE; BENZYLOXYCABONYLALLENE; SULFONYLALLENE; UNCLASSIFIED DRUG;

EID: 54549120166     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.09.069     Document Type: Article
Times cited : (16)

References (49)
  • 6
    • 54549105790 scopus 로고    scopus 로고
    • For exo-mode ring-closing reaction of allenyl sulfoxide derivatives, see:
    • For exo-mode ring-closing reaction of allenyl sulfoxide derivatives, see:
  • 9
    • 54549103496 scopus 로고    scopus 로고
    • For exo-mode ring-closing reaction of allenyl sulfone derivatives, see:
    • For exo-mode ring-closing reaction of allenyl sulfone derivatives, see:
  • 11
    • 54549093882 scopus 로고    scopus 로고
    • For exo-mode ring-closing reaction of allenylphosphonate derivatives, see:
    • For exo-mode ring-closing reaction of allenylphosphonate derivatives, see:
  • 17
    • 54549091183 scopus 로고    scopus 로고
    • For other examples of endo-mode ring-closing reaction of allenyl ester derivatives, see:
    • For other examples of endo-mode ring-closing reaction of allenyl ester derivatives, see:
  • 20
    • 54549109131 scopus 로고    scopus 로고
    • For our other studies on the endo-mode ring-closing reaction of allenic compounds, see:
    • For our other studies on the endo-mode ring-closing reaction of allenic compounds, see:
  • 29
    • 54549100454 scopus 로고    scopus 로고
    • Yoshimoto and Kishida reported that the treatment of 2-butynyl phenyl sulfone and substituted benzaldehyde with NaH afforded many products derived from γ-adduct (based on the condensation of allenyl anion with aldehyde). See:
    • Yoshimoto and Kishida reported that the treatment of 2-butynyl phenyl sulfone and substituted benzaldehyde with NaH afforded many products derived from γ-adduct (based on the condensation of allenyl anion with aldehyde). See:
  • 32
    • 38349042210 scopus 로고    scopus 로고
    • Hammond and co-worker reported that propargyl or allenyl esters reacted with aldehydes in the presence of 2 equiv of TBAF to produce γ-adduct. See:
    • Hammond and co-worker reported that propargyl or allenyl esters reacted with aldehydes in the presence of 2 equiv of TBAF to produce γ-adduct. See:. Xu B., and Hammond G.B. Angew. Chem., Int. Ed. 47 (2008) 689-692
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 689-692
    • Xu, B.1    Hammond, G.B.2
  • 33
    • 54549122665 scopus 로고    scopus 로고
    • For condensation of allenyl esters or allenyl ketones with aldehydes or imines based on Baylis-Hillman reaction, see:
    • For condensation of allenyl esters or allenyl ketones with aldehydes or imines based on Baylis-Hillman reaction, see:
  • 36
    • 54549102346 scopus 로고    scopus 로고
    • For examples, see:
    • For examples, see:
  • 46


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.