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Volumn 62, Issue 14, 1997, Pages 4568-4569

Novel Coupling Reactions of Dithioacetals with Organocuprate Reagents. Propargylic Dithioacetal as an Allene-1,3-Zwitterion Synthon

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EID: 0000162191     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970700v     Document Type: Article
Times cited : (21)

References (25)
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    • For reviews, see: (a) Naso, F. Pure Appl. Chem. 1988, 60, 79. (b) Fiandanese, V. Pure Appl. Chem. 1990, 62, 1987.
    • (1988) Pure Appl. Chem. , vol.60 , pp. 79
    • Naso, F.1
  • 2
    • 0000204040 scopus 로고
    • For reviews, see: (a) Naso, F. Pure Appl. Chem. 1988, 60, 79. (b) Fiandanese, V. Pure Appl. Chem. 1990, 62, 1987.
    • (1990) Pure Appl. Chem. , vol.62 , pp. 1987
    • Fiandanese, V.1
  • 4
    • 0000250430 scopus 로고
    • For reviews, see: (a) Luh, T.-Y. Acc. Chem. Res. 1991, 24, 257. (b) Luh, T.-Y.; Leung, M.-K. In Advances in the Use of Synthons in Organic Chemistry; Dondoni, A., Ed.; JAI: London, 1995; Vol. 2, 129. Luh, T.-Y. Pure Appl. Chem. 1996, 68, 105.
    • (1991) Acc. Chem. Res. , vol.24 , pp. 257
    • Luh, T.-Y.1
  • 5
    • 0000250430 scopus 로고
    • Dondoni, A., Ed.; JAI: London
    • For reviews, see: (a) Luh, T.-Y. Acc. Chem. Res. 1991, 24, 257. (b) Luh, T.-Y.; Leung, M.-K. In Advances in the Use of Synthons in Organic Chemistry; Dondoni, A., Ed.; JAI: London, 1995; Vol. 2, 129. Luh, T.-Y. Pure Appl. Chem. 1996, 68, 105.
    • (1995) Advances in the use of Synthons in Organic Chemistry , vol.2 , pp. 129
    • Luh, T.-Y.1    Leung, M.-K.2
  • 6
    • 0000956140 scopus 로고    scopus 로고
    • For reviews, see: (a) Luh, T.-Y. Acc. Chem. Res. 1991, 24, 257. (b) Luh, T.-Y.; Leung, M.-K. In Advances in the Use of Synthons in Organic Chemistry; Dondoni, A., Ed.; JAI: London, 1995; Vol. 2, 129. Luh, T.-Y. Pure Appl. Chem. 1996, 68, 105.
    • (1996) Pure Appl. Chem. , vol.68 , pp. 105
    • Luh, T.-Y.1
  • 16
    • 1542585956 scopus 로고
    • Schlosser, M., Ed.; Wiley: Chichester;, Chapter 4
    • HMPA was essential for the alkylation with MeI or allyl bromide under these conditions (Table 1, entries 7 and 8). The yield was otherwise much lower. (Cf. Lipshutz, B. H. In Organometallics in Synthesis; Schlosser, M., Ed.; Wiley: Chichester, 1994; Chapter 4.)
    • (1994) Organometallics in Synthesis
    • Lipshutz, B.H.1


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