-
1
-
-
20544450502
-
-
De Meijere, A, Diederich, F, Eds, Wiley-VCH: Weinheim
-
(a) De Meijere, A., Diederich, F., Eds. Metal-Catalyzed Cross-Coupling Reactions; Wiley-VCH: Weinheim, 2004.
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
-
-
-
2
-
-
27844611828
-
-
Tsuji, J, Ed, Springer-Verlag: Berlin
-
(b) Tsuji, J., Ed. Topics in Organometallic Chemistry; Springer-Verlag: Berlin 2005; Vol. 14.
-
(2005)
Topics in Organometallic Chemistry
, vol.14
-
-
-
4
-
-
0001038733
-
-
(b) Wolfe, J. P.; Wagaw, S.; Marcoux, J.; Buchwald, S. L. Acc. Chem. Res. 1998, 31, 805.
-
(1998)
Acc. Chem. Res
, vol.31
, pp. 805
-
-
Wolfe, J.P.1
Wagaw, S.2
Marcoux, J.3
Buchwald, S.L.4
-
5
-
-
0034677864
-
-
(c) Beller, M.; Eckert, M. Angew. Chem., Int. Ed. 2000, 39, 1010.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 1010
-
-
Beller, M.1
Eckert, M.2
-
6
-
-
35548985485
-
-
2 and other element-element bonds: Makabe, H.; Negishi, E. Handb. Organopalladium Chem. Org. Synth. 2002, 2, 2789.
-
2 and other element-element bonds: Makabe, H.; Negishi, E. Handb. Organopalladium Chem. Org. Synth. 2002, 2, 2789.
-
-
-
-
7
-
-
35548971704
-
-
For reviews of C-O oxidative addition: (a) Yamamoto, A. Advances in Organometallic Chemistry; Academic Press: San Diego, 1992; 34.
-
For reviews of C-O oxidative addition: (a) Yamamoto, A. Advances in Organometallic Chemistry; Academic Press: San Diego, 1992; Vol. 34.
-
-
-
-
8
-
-
0003464697
-
-
Murai, S, Ed, Springer-Verlag: Berlin
-
(b) Lin, Y. S.; Yamamoto, A. Topics in Organometallic Chemstry; Murai, S., Ed.; Springer-Verlag: Berlin, 1999; Vol. 3.
-
(1999)
Topics in Organometallic Chemstry
, vol.3
-
-
Lin, Y.S.1
Yamamoto, A.2
-
9
-
-
0032496954
-
-
(a) van der Boom, M. E.; Liou, S. Y.; Ben-David, Y.; Shimon, L. J. W.; Milstein, D. J. J. Am. Chem. Soc. 1998, 120, 6531.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 6531
-
-
van der Boom, M.E.1
Liou, S.Y.2
Ben-David, Y.3
Shimon, L.J.W.4
Milstein, D.J.5
-
10
-
-
0001426376
-
-
(b) Yamamoto, T.; Akimoto, M.; Saito, O.; Yamamoto, A. Organometallics 1986, 5, 1559.
-
(1986)
Organometallics
, vol.5
, pp. 1559
-
-
Yamamoto, T.1
Akimoto, M.2
Saito, O.3
Yamamoto, A.4
-
11
-
-
35548986326
-
-
Allylic ethers: (a) Acemoglu, L.; Williams, J. M. J. Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley: Weinhiem, 2002; pp 1689.
-
Allylic ethers: (a) Acemoglu, L.; Williams, J. M. J. Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley: Weinhiem, 2002; pp 1689.
-
-
-
-
13
-
-
0032499992
-
-
(c) Cacchi, S.; Fabrizi, G.; Moro, L. Tetrahedron Lett. 1998, 39, 5101.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 5101
-
-
Cacchi, S.1
Fabrizi, G.2
Moro, L.3
-
14
-
-
0141741339
-
-
Others
-
(d) Pal, M.; Parasuraman, K.; Yeleswarapu, R. Org. Lett. 2003, 5, 349. Others:
-
(2003)
Org. Lett
, vol.5
, pp. 349
-
-
Pal, M.1
Parasuraman, K.2
Yeleswarapu, R.3
-
15
-
-
1542377701
-
-
(e) Kakiuchi, F.; Usui, M.; Uedo, S.; Chatani, N.; Murai, S. J. Am. Chem. Soc. 2004, 126, 2706.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 2706
-
-
Kakiuchi, F.1
Usui, M.2
Uedo, S.3
Chatani, N.4
Murai, S.5
-
16
-
-
0034674275
-
-
(a) Sajiki, H.; Hattori, K.; Hirota, K. Chem. Eur. J. 2000, 6, 2200.
-
(2000)
Chem. Eur. J
, vol.6
, pp. 2200
-
-
Sajiki, H.1
Hattori, K.2
Hirota, K.3
-
18
-
-
0033590532
-
-
Including amidocarbonylation (ref 2c) and the Monsanto acid process: Yang, J.; Haynes, A.; Maitlis, P. M. Chem. Commun. 1999, 179.
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Including amidocarbonylation (ref 2c) and the Monsanto acid process: Yang, J.; Haynes, A.; Maitlis, P. M. Chem. Commun. 1999, 179.
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-
-
19
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0037433246
-
-
(a) Dhawan, R.; Dghaym, R. D.; Arndtsen, B. A. J. Am. Chem. Soc. 2003, 125, 1474.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 1474
-
-
Dhawan, R.1
Dghaym, R.D.2
Arndtsen, B.A.3
-
22
-
-
33748931448
-
-
(d) Dhawan, R.; Dghaym, R. D.; St. Cyr, D. J.; Arndtsen, B. A. Org. Lett. 2006, 8, 3927.
-
(2006)
Org. Lett
, vol.8
, pp. 3927
-
-
Dhawan, R.1
Dghaym, R.D.2
St. Cyr, D.J.3
Arndtsen, B.A.4
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25
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35548967230
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This ionization suggests 2a is better considered as an intermediate in an ionic oxidative addition, rather than a formal oxidative addition product
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This ionization suggests 2a is better considered as an intermediate in an ionic oxidative addition, rather than a formal oxidative addition product.
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26
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35548991558
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3.
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3.
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27
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35549011579
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The use of phenoxyamides 1 also obviates the need for a second step of addition of alcohols to the in situ generated münchnone ref 9a, making this an operationally more straightforward amino acid synthesis
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The use of phenoxyamides 1 also obviates the need for a second step of addition of alcohols to the in situ generated münchnone (ref 9a), making this an operationally more straightforward amino acid synthesis.
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