메뉴 건너뛰기




Volumn , Issue 6, 1998, Pages 557-565

It takes alkynes to make a world - New methods for dehydrobenzoannulene synthesis

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001083913     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-5736     Document Type: Article
Times cited : (72)

References (75)
  • 16
    • 0039160738 scopus 로고
    • (b) Simpson, M. New Sci. 1988, 117(1603), 50.
    • (1988) New Sci. , vol.117 , Issue.1603 , pp. 50
    • Simpson, M.1
  • 25
    • 0001529667 scopus 로고    scopus 로고
    • For an alternate cyclooligomerization synthesis of 4 (three steps from phenylacetylene, 24% overall yield) and numerous references of its use as a ligand in organometallic chemistry, see: Solooki, D.; Ferrara, J. D.; Malaba, D.; Bradshaw, J. D.; Tessier, C. A.; Youngs, W. J. Inorg. Synth. 1997, 31, 122.
    • (1997) Inorg. Synth. , vol.31 , pp. 122
    • Solooki, D.1    Ferrara, J.D.2    Malaba, D.3    Bradshaw, J.D.4    Tessier, C.A.5    Youngs, W.J.6
  • 27
    • 0001350591 scopus 로고
    • Stang, P. J.; Diederich, F. (Eds.); VCH: Weinheim
    • (b) Diederich, F. in Modern Acetylene Chemistry, Stang, P. J.; Diederich, F. (Eds.); VCH: Weinheim, 1995, p 443.
    • (1995) Modern Acetylene Chemistry , pp. 443
    • Diederich, F.1
  • 29
    • 0001854116 scopus 로고
    • Stang, P. J.; Diederich, F. (Eds.); VCH: Weinheim
    • (b) Young, J. K.; Moore, J. S. in Modern Acetylene Chemistry, Stang, P. J.; Diederich, F. (Eds.); VCH: Weinheim, 1995, p 415.
    • (1995) Modern Acetylene Chemistry , pp. 415
    • Young, J.K.1    Moore, J.S.2
  • 36
    • 26844476617 scopus 로고    scopus 로고
    • note
    • Josh Kehoe, Ryan Petersen, and Charles Johnson were the unfortunate souls to have gotten stuck with all the variations towards 8b. I gratefully acknowledge their many efforts.
  • 37
    • 26844546104 scopus 로고    scopus 로고
    • note
    • Robert Schneidmiller of Professor David Johnson's laboratory at Oregon has kindly provided us with all of the needed DSC results over the last 2+ years.
  • 40
    • 26844447047 scopus 로고    scopus 로고
    • note
    • Adam Matzger, the talented graduate student who prepared 19, joined Peter's group just as I left for Oregon; thus, I was unaware of the projects Peter had him exploring.
  • 41
    • 0003833714 scopus 로고
    • Martinus Nijhoff: Boston
    • (a) Polydiacetylenes, Bloor, D.; Chance, R. R. (Eds.); Martinus Nijhoff: Boston, 1985, and references therein.
    • (1985) Polydiacetylenes
    • Bloor, D.1    Chance, R.R.2
  • 44
    • 0001547013 scopus 로고    scopus 로고
    • The first edition of reference 17a contained the preparation of the parent molecule, but stated that the diyne proved to be very unstable. Other groups have reported similar problems using free phenylbutadiynes in synthesis; see: Godt, A. J. Org. Chem. 1997, 62, 7471.
    • (1997) J. Org. Chem. , vol.62 , pp. 7471
    • Godt, A.1
  • 46
    • 26844543490 scopus 로고    scopus 로고
    • note
    • Work on macrocycles 23 and 24 is currently in progress by Stephen Brand.
  • 49
    • 0000464034 scopus 로고
    • Although the synthesis of phenylhexatriynes has been previously reported, no yields were included in the paper. The only identification of the products was by UV spectroscopy. See: Eastmond, R.; Walton, D. M. R. Tetrahedron 1972, 28, 4591.
    • (1972) Tetrahedron , vol.28 , pp. 4591
    • Eastmond, R.1    Walton, D.M.R.2
  • 59
    • 26844544275 scopus 로고    scopus 로고
    • manuscript in preparation
    • Pak, J. J.; Haley, M. M., manuscript in preparation.
    • Pak, J.J.1    Haley, M.M.2
  • 73
    • 26844443315 scopus 로고    scopus 로고
    • note
    • Semi-empirical calculations (AM1, PM3) were performed on a SGI workstation using Spartan molecular modelling software (Version 4.1.1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.