-
1
-
-
0004294109
-
-
Viehe, H. G. Marcel Dekker: New York
-
Winterfeldt, E.; Julia, M.; Gutmann, H.; Lindlar, H.; Wotiz, J. H.; Fuks, R.; Viehe, H. G. In Chemistry of Acetylenes; Viehe, H. G., Ed.; Marcel Dekker: New York, 1969; pp 265-588.
-
(1969)
Chemistry of Acetylenes
, pp. 265-588
-
-
Winterfeldt, E.1
Julia, M.2
Gutmann, H.3
Lindlar, H.4
Wotiz, J.H.5
Fuks, R.6
Viehe, H.G.7
-
8
-
-
0000595175
-
-
Fleming, I.; Barbero, A.; Walter, D. Chem. Rev. 1997, 97, 2063
-
(1997)
Chem. Rev.
, vol.97
, pp. 2063
-
-
Fleming, I.1
Barbero, A.2
Walter, D.3
-
10
-
-
77951169903
-
-
Denmark, S. E.; Liu, J. H.-C. Angew. Chem., Int. Ed. 2010, 49, 2978
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 2978
-
-
Denmark, S.E.1
Liu, J.H.-C.2
-
11
-
-
57249103666
-
-
Nishimoto, Y.; Kajioka, M.; Saito, T.; Yasuda, M.; Baba, A. Chem. Commun. 2008, 6396
-
(2008)
Chem. Commun.
, pp. 6396
-
-
Nishimoto, Y.1
Kajioka, M.2
Saito, T.3
Yasuda, M.4
Baba, A.5
-
13
-
-
77951165523
-
-
Liu, L.; Floreancig, P. E. Angew. Chem., Int. Ed. 2010, 49, 3069
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 3069
-
-
Liu, L.1
Floreancig, P.E.2
-
15
-
-
33748937863
-
-
Murakami, M.; Sakita, K.; Igawa, K.; Tomooka, K. Org. Lett. 2006, 8, 4023
-
(2006)
Org. Lett.
, vol.8
, pp. 4023
-
-
Murakami, M.1
Sakita, K.2
Igawa, K.3
Tomooka, K.4
-
16
-
-
44949233104
-
-
Igawa, K.; Sakita, K.; Murakami, M.; Tomooka, K. Synthesis 2008, 1641
-
(2008)
Synthesis
, pp. 1641
-
-
Igawa, K.1
Sakita, K.2
Murakami, M.3
Tomooka, K.4
-
17
-
-
79951906222
-
-
Igawa, K.; Kawasaki, Y.; Tomooka, K. Chem. Lett. 2011, 40, 233
-
(2011)
Chem. Lett.
, vol.40
, pp. 233
-
-
Igawa, K.1
Kawasaki, Y.2
Tomooka, K.3
-
18
-
-
22244480386
-
-
Trost et al. reported an efficient approach for oxy-functionalized compounds from Z -silylalkenes by Ru-catalyzed hydrosilylation of alkynes
-
Trost et al. reported an efficient approach for oxy-functionalized compounds from Z -silylalkenes by Ru-catalyzed hydrosilylation of alkynes: Trost, B. M.; Ball, Z. T.; Laemmerhold, K. M. J. Am. Chem. Soc. 2005, 127, 10028
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10028
-
-
Trost, B.M.1
Ball, Z.T.2
Laemmerhold, K.M.3
-
19
-
-
0001237287
-
-
Tamao, K.; Maeda, K.; Tanaka, T.; Ito, Y. Tetrahedoron Lett. 1988, 29, 6955
-
(1988)
Tetrahedoron Lett.
, vol.29
, pp. 6955
-
-
Tamao, K.1
Maeda, K.2
Tanaka, T.3
Ito, Y.4
-
23
-
-
0037134173
-
-
Itami, K.; Mitsudo, K.; Nishino, A.; Yoshida, J. J. Org. Chem. 2002, 67, 2645
-
(2002)
J. Org. Chem.
, vol.67
, pp. 2645
-
-
Itami, K.1
Mitsudo, K.2
Nishino, A.3
Yoshida, J.4
-
25
-
-
40849112912
-
-
Hamze, A.; Provot, O.; Brion, J.-D.; Alami, M. Tetrahedoron Lett. 2008, 49, 2429
-
(2008)
Tetrahedoron Lett.
, vol.49
, pp. 2429
-
-
Hamze, A.1
Provot, O.2
Brion, J.-D.3
Alami, M.4
-
26
-
-
44949261091
-
-
Berthon-Gelloz, G.; Schumers, J.-M.; Bo, G. D.; Markó, I. E. J. Org. Chem. 2008, 73, 4190
-
(2008)
J. Org. Chem.
, vol.73
, pp. 4190
-
-
Berthon-Gelloz, G.1
Schumers, J.-M.2
Bo, G.D.3
Markó, I.E.4
-
27
-
-
65749115629
-
-
Blug, M.; Goff, X.-F. L.; Mézailles, N.; Floch, P. L. Organometallics 2009, 28, 2360
-
(2009)
Organometallics
, vol.28
, pp. 2360
-
-
Blug, M.1
Goff, X.-F.L.2
Mézailles, N.3
Floch, P.L.4
-
28
-
-
84555183293
-
-
U.S. Patent 3419593
-
Willing, D. N. U.S. Patent 3419593, 1968.
-
(1968)
-
-
Willing, D.N.1
-
29
-
-
84555182094
-
-
U.S. Patent 3775452
-
Karstedt, B. D. U.S. Patent 3775452, 1973.
-
(1973)
-
-
Karstedt, B.D.1
-
30
-
-
18944383666
-
-
Lewis, L. N.; Sy, K. G.; Bryant., G. L., Jr.; Donahue, P. E. Organometallics 1991, 10, 3750
-
(1991)
Organometallics
, vol.10
, pp. 3750
-
-
Lewis, L.N.1
Sy, K.G.2
Bryant Jr., G.L.3
Donahue, P.E.4
-
31
-
-
0000665822
-
-
Stork, G.; Jung, M. E.; Colvin, E.; Noel, Y. J. Am. Chem. Soc. 1974, 96, 3684
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 3684
-
-
Stork, G.1
Jung, M.E.2
Colvin, E.3
Noel, Y.4
-
33
-
-
36749010679
-
-
Brookhart et al. reported Co-catalyzed intramolecular hydrogen transfer from an amine moiety to a DMVS group and proposed that DMVS acts as a DG
-
Brookhart et al. reported Co-catalyzed intramolecular hydrogen transfer from an amine moiety to a DMVS group and proposed that DMVS acts as a DG: Bolig, A. D.; Brookhart, M. J. Am. Chem. Soc. 2007, 129, 14544
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 14544
-
-
Bolig, A.D.1
Brookhart, M.2
-
34
-
-
1842607439
-
-
Miller, K. M.; Luanphaisarnnont, T.; Molinaro, C.; Jamison, T. F. J. Am. Chem. Soc. 2004, 126, 4130
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 4130
-
-
Miller, K.M.1
Luanphaisarnnont, T.2
Molinaro, C.3
Jamison, T.F.4
-
36
-
-
33745420514
-
-
Moslin, R. M.; Miller, K. M.; Jamison, T. F. Tetrahedron 2006, 62, 7598
-
(2006)
Tetrahedron
, vol.62
, pp. 7598
-
-
Moslin, R.M.1
Miller, K.M.2
Jamison, T.F.3
-
38
-
-
33645801391
-
-
Tsipis and Kefalidis reported a pioneering theoretical study on alkyne hydrosilylation using a Pt(0) catalyst, where acetylene and phosphane were used as substrate and ligand, respectively
-
Tsipis and Kefalidis reported a pioneering theoretical study on alkyne hydrosilylation using a Pt(0) catalyst, where acetylene and phosphane were used as substrate and ligand, respectively: Tsipis, C. A.; Kefalidis, C. E. Organometallics 2006, 25, 1696
-
(2006)
Organometallics
, vol.25
, pp. 1696
-
-
Tsipis, C.A.1
Kefalidis, C.E.2
-
39
-
-
0001900153
-
-
These results clearly indicate that hydrosilylation of TBS ether 7 is faster than that of alkyne 16. Regarding the substituent effect of the oxy-functional group at the propargylic position, Tsipis reported that hydrosilylation of propargylic alcohols is faster than that of non-substituted alkynes
-
These results clearly indicate that hydrosilylation of TBS ether 7 is faster than that of alkyne 16. Regarding the substituent effect of the oxy-functional group at the propargylic position, Tsipis reported that hydrosilylation of propargylic alcohols is faster than that of non-substituted alkynes: Tsipis, C. A. J. Organomet. Chem. 1980, 188, 53
-
(1980)
J. Organomet. Chem.
, vol.188
, pp. 53
-
-
Tsipis, C.A.1
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