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Volumn 71, Issue 13, 2006, Pages 4937-4942

Synthesis of substituted benzoxacycles via a domino ortho-alkylation/heck coupling sequence

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLIDENE BENZOXACYCLES; BENZOXACYCLES; HECK REACTION; NORBORNENE;

EID: 33745478478     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060552l     Document Type: Article
Times cited : (51)

References (45)
  • 1
    • 15944396476 scopus 로고    scopus 로고
    • Choromans are typically found as the core of the tocopherols, most importantly Vitamin E (α-tocopherol). For the subtype-specific translocation and activation of diacylglycerol kinase α by D-α-tocopherol, see: (a) Fukunaga-Takenaka, R.; Shirai, Y.; Yagi, K.; Adachi, N.; Sakai, N.; Merino, E.; Merida, I.; Saito, N. Genes Cells 2005, 10, 311-319.
    • (2005) Genes Cells , vol.10 , pp. 311-319
    • Fukunaga-Takenaka, R.1    Shirai, Y.2    Yagi, K.3    Adachi, N.4    Sakai, N.5    Merino, E.6    Merida, I.7    Saito, N.8
  • 3
    • 33745444560 scopus 로고    scopus 로고
    • WO 2004103985, 2004
    • For the use of chromans in the treatment of cancer and inflammation, see: (c) Salvatore, B. A.; Solis, F. C. WO 2004103985, 2004.
    • Salvatore, B.A.1    Solis, F.C.2
  • 28
    • 0035323796 scopus 로고    scopus 로고
    • For a review of the use of tri(2-furyl)phosphine in transition metal mediated reactions, see: Andersen, N. G.; Keay, B. G. Chem. Rev. 2001, 101, 997-1030.
    • (2001) Chem. Rev. , vol.101 , pp. 997-1030
    • Andersen, N.G.1    Keay, B.G.2
  • 29
    • 33745451637 scopus 로고
    • Small Ring Heterocycles; Hassner, A., Ed.; John Wiley & Sons: Toronto, Canada
    • Hassner, A. In Heterocyclic Compounds; Vol. 42, Part 3, Small Ring Heterocycles; Hassner, A., Ed.; John Wiley & Sons: Toronto, Canada, 1985; pp 3-152.
    • (1985) Heterocyclic Compounds , vol.42 , Issue.PART 3 , pp. 3-152
    • Hassner, A.1
  • 30
    • 33745439995 scopus 로고    scopus 로고
    • We have preliminary results for a domino ortho-alkylation/aromatic amination reaction
    • We have preliminary results for a domino ortho-alkylation/aromatic amination reaction.
  • 31
    • 21144468068 scopus 로고
    • For synthetic applications of Weinreb amides, see: (a) Sibi, M. P. Org. Prep. Proc. Int. 1993, 25, 15-42.
    • (1993) Org. Prep. Proc. Int. , vol.25 , pp. 15-42
    • Sibi, M.P.1
  • 34
    • 0001454786 scopus 로고
    • For a discussion on the effect of electron donating and withdrawing groups on the rate of oxidative addition, see: Amatore, C.; Pflüger, F. Organometallics 1990, 9, 2276-2282.
    • (1990) Organometallics , vol.9 , pp. 2276-2282
    • Amatore, C.1    Pflüger, F.2
  • 38
    • 0347985383 scopus 로고    scopus 로고
    • In Sonogashira coupling, particularly with ortho-substituted aryl chlorides, see: (c) Gelman, D.; Buchwald, S. L. Angew. Chem., Int. Ed. 2003, 42, 5993-5996.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5993-5996
    • Gelman, D.1    Buchwald, S.L.2
  • 39
    • 0030878818 scopus 로고    scopus 로고
    • In Suzuki-Miyaura coupling, see: (d) Shen, W. Tetrahedron Lett. 1997, 38, 5575-5578.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5575-5578
    • Shen, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.