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1
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Ed, S. Patai, Wiley, New York, Chapter 10;
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a) J.-L. Moreau, The Chemistry of Ketenes, Alienes, and Related Compounds, (Ed.: S. Patai), Wiley, New York, 1980, Chapter 10;
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The Chemistry of Ketenes, Alienes, and Related Compounds
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Moreau, J.-L.1
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2
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0003399091
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Elsevier; Amsterdam, Chapter III;
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b) L. Brandsma, H. D. Verkruijsse, Synthesis of Acetylenes, Alienes and Cumulenes, Elsevier; Amsterdam, 1981, Chapter III;
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(1981)
Synthesis of Acetylenes, Alienes and Cumulenes
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Brandsma, L.1
Verkruijsse, H.D.2
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3
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0003716367
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Ed, B. M. Trost, Pergamon Press, Oxford, Chapter 1.3
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c) H. Yamamoto, Comprehensive Organic Synthesis, Vol. 2, (Ed.: B. M. Trost), Pergamon Press, Oxford, 1991, Chapter 1.3.
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(1991)
Comprehensive Organic Synthesis
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Yamamoto, H.1
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4
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0010646875
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For examples: a
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For examples: a) N. R. Pearson, G. Hahn, G. Zweifel, J. Org. Chem. 1982, 47, 3364-3366;
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(1982)
J. Org. Chem
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Pearson, N.R.1
Hahn, G.2
Zweifel, G.3
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5
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0000498840
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b) M. Ishiguro, N. Ikeda, H. Yamamoto, J. Org. Chem. 1982, 47, 2225-2227;
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(1982)
J. Org. Chem
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Ishiguro, M.1
Ikeda, N.2
Yamamoto, H.3
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6
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0010690719
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c)K. K. Wang, S. S. Nikam, C. D. Ho, J. Org. Chem. 1983, 48, 5376-5377;
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(1983)
J. Org. Chem
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Wang, K.K.1
Nikam, S.S.2
Ho, C.D.3
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7
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0000986355
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d) K. Furuta, M. Ishiguro, R. Haruta, N. Ikeda, H. Yamamoto, Bull. Chem. Soc. Jpn. 1984, 57, 2768-2776;
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(1984)
Bull. Chem. Soc. Jpn
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Furuta, K.1
Ishiguro, M.2
Haruta, R.3
Ikeda, N.4
Yamamoto, H.5
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9
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0001429190
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f) C. Meyer, I. Marek, G. Courtemanche, J.-F. Normant, J. Org. Chem. 1995, 60, 863-871;
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(1995)
J. Org. Chem
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Meyer, C.1
Marek, I.2
Courtemanche, G.3
Normant, J.-F.4
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12
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0142248461
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i) T. P. Hoffman, J. D. Trenkle, T. F. Jamison, Tetrahedron 2003, 59, 8913-8917;
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(2003)
Tetrahedron
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Hoffman, T.P.1
Trenkle, J.D.2
Jamison, T.F.3
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14
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17444428902
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j) S. Ma, Q. He, X. Zhang, J. Org. Chem. 2005, 70, 3336-3338.
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(2005)
J. Org. Chem
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Ma, S.1
He, Q.2
Zhang, X.3
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15
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0032494413
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Palladium-catalyzed C-C bond formation of acetylenes via allenes giving substituted alkenes was reported. For recent examples: a I. Kadota, A. Shibuya, Y. S. Gyoung, Y Yamamoto, J. Am. Chem. Soc. 1998, 120, 10262-10263;
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Palladium-catalyzed C-C bond formation of acetylenes via allenes giving substituted alkenes was reported. For recent examples: a) I. Kadota, A. Shibuya, Y. S. Gyoung, Y Yamamoto, J. Am. Chem. Soc. 1998, 120, 10262-10263;
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16
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4143123249
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b) N. T. Patil, I. Kadota, A. Shibuya, Y. S. Gyoung, Y. Yamamoto, Adv. Synth. Catai. 2004, 346, 800-804;
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(2004)
Adv. Synth. Catai
, vol.346
, pp. 800-804
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Patil, N.T.1
Kadota, I.2
Shibuya, A.3
Gyoung, Y.S.4
Yamamoto, Y.5
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17
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5644300523
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c) N. T. Patil, F. N. Khan, Y. Yamamoto, Tetrahedron Lett. 2004, 45, 8497-8499.
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(2004)
Tetrahedron Lett
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, pp. 8497-8499
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Patil, N.T.1
Khan, F.N.2
Yamamoto, Y.3
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18
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0001353318
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Lanthanum- and cerium-catalyzed cyclodimerization of methyl acetylenes via propargyl activation was reported: H. J. Heeres, A. Heeres, J. H. Teuben, Organometallics 1990, 9, 1508-1510
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Lanthanum- and cerium-catalyzed cyclodimerization of methyl acetylenes via propargyl activation was reported: H. J. Heeres, A. Heeres, J. H. Teuben, Organometallics 1990, 9, 1508-1510.
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19
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20444503312
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R. Amemiya. K. Suwa, J. Toriyama, Y. Nishimura, M. Yamaguchi, J. Am. Chem. Soc. 2005, 127, 8252-8253.
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(2005)
J. Am. Chem. Soc
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Amemiya, R.1
Suwa, K.2
Toriyama, J.3
Nishimura, Y.4
Yamaguchi, M.5
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20
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0142025030
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3: a R. Amemiya, A. Fujii, M. Arisawa, M. Yamaguchi, J. Organomet. Chem. 2003, 686, 94-100;
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3: a) R. Amemiya, A. Fujii, M. Arisawa, M. Yamaguchi, J. Organomet. Chem. 2003, 686, 94-100;
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21
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0037167002
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b) K. Kobayashi, M. Arisawa, M. Yamaguchi, J. Am. Chem. Soc. 2002, 124, 8528-8529;
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(2002)
J. Am. Chem. Soc
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, pp. 8528-8529
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Kobayashi, K.1
Arisawa, M.2
Yamaguchi, M.3
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22
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2342497222
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c) R. Amemiya, A. Fujii, M. Yamaguchi, Tetrahedron Lett. 2004, 45, 4333-4335;
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(2004)
Tetrahedron Lett
, vol.45
, pp. 4333-4335
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Amemiya, R.1
Fujii, A.2
Yamaguchi, M.3
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24
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32244437968
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also see, the direct ethynylation reaction of ketone using a catalytic amount of trialkylgallium: Y. Nishimura, R. Amemiya, M. Yamaguchi, Tetrahedron Lett. 2006, 47, 1797-1800.
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also see, the direct ethynylation reaction of ketone using a catalytic amount of trialkylgallium: Y. Nishimura, R. Amemiya, M. Yamaguchi, Tetrahedron Lett. 2006, 47, 1797-1800.
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25
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0030848347
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3 was reported in our previous works: a M. Yamaguchi, Y. Kido, A. Hayashi, M. Hirama, Angew. Chem. Int. Ed. 1997, 36, 1313-1315;
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3 was reported in our previous works: a) M. Yamaguchi, Y. Kido, A. Hayashi, M. Hirama, Angew. Chem. Int. Ed. 1997, 36, 1313-1315;
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26
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0032765847
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b) Y. Kido, S. Yoshimura, M. Yamaguchi, T. Uchimaru, Bull. Chem. Soc. Jpn., 1999, 72, 1445-1458.
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(1999)
Bull. Chem. Soc. Jpn
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, pp. 1445-1458
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Kido, Y.1
Yoshimura, S.2
Yamaguchi, M.3
Uchimaru, T.4
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27
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0001514241
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The low-field shift of silylacetylene by metal complexation is known for Ti and Zr derivatives: a A. Ohff, P. Kosse, W. Baumann, A. Tillack, R. Kempe, H. Görls, V. V. Burlakov, U. Rosenthal, J. Am. Chem. Soc. 1995, 117, 10399-10400;
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The low-field shift of silylacetylene by metal complexation is known for Ti and Zr derivatives: a) A. Ohff, P. Kosse, W. Baumann, A. Tillack, R. Kempe, H. Görls, V. V. Burlakov, U. Rosenthal, J. Am. Chem. Soc. 1995, 117, 10399-10400;
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28
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0031665039
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b) N. Peulecke, A. Ohff, P. Kosse, A. Tillack, A. Spannenberg, R. Kempe, W. Baumann, V. V. Burlakov, U. Rosenthal . Chem. Eur. J. 1998, 4, 1852-1861.
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(1998)
Chem. Eur. J
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, pp. 1852-1861
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Peulecke, N.1
Ohff, A.2
Kosse, P.3
Tillack, A.4
Spannenberg, A.5
Kempe, R.6
Baumann, W.7
Burlakov, V.V.8
Rosenthal, U.9
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