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For a review, see, (in Japanese)
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The palladium-catalyzed cross-coupling reactions of organotin reagents with organic electrophiles
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Stille, J. K., The palladium-catalyzed cross-coupling reactions of organotin reagents with organic electrophiles. Angew. Chem. Int. Ed. Engl., 25, 508-524 (1986).
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Stille, J.K.1
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Mitchell, T. N., Palladium-catalyzed reactions of organotin compounds. Synthesis, 803-815 (1992).
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Mitchell, T.N.1
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7
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For example
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Trost, B.M.1
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Palladium-catalyzed cross coupling of allyl halides with organotin reagents: A method of joining highly functionalized partners regioselectively and stereospecifically
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Sheffy, F. K., Godscalx, J. P., and Stille, J. K., Palladium-catalyzed cross coupling of allyl halides with organotin reagents: A method of joining highly functionalized partners regioselectively and stereospecifically. J. Am. Chem. Soc., 106, 4833-4840 (1984).
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Sheffy, F.K.1
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9
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0002810752
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A new catalytic synthesis of non-con-jugated alkenynes
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Nickel(0) catalyzed coupling of an allylic ester with terminal acetylene was reported
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catalyzed coupling of an allylic ester with terminal acetylene was reported: Gatellani, M., Chiusoli, G. P., Salerno, G., and Dallatomasina, F., A new catalytic synthesis of non-con-jugated alkenynes. J. Organomet. Chem., 146, C19-C22 (1978).
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Gatellani, M.1
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11
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0025048932
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Palladium catalysts in cephalosporin chemistry: General methodology for the synthesis of cephem side chain
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Farina, V., Baker, S. R., Benigni, D. A., Hauck, S. I., and Sapino, Jr., C., Palladium catalysts in cephalosporin chemistry: General methodology for the synthesis of cephem side chain. J. Org. Chem., 55, 5833-5847 (1990).
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84986531866
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Methodologies for Synthesis of Heterocyclic Compounds
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Isobe, M., Nishikawa, T., Yamamoto, N., Tsukiyama, T., Ino, A., and Okita, T., Methodologies for Synthesis of Heterocyclic Compounds. J. Heterocycl. Chem., 29, 619-625 (1992).
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Isobe, M.1
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13
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0003853085
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Synthetic studies toward enediyne antitumor antibiotics
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Krohn, K., Krist, H., and Maag, H. VCH, Weinheim
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Isobe, M., and Nishikawa, T., Synthetic studies toward enediyne antitumor antibiotics. In “Antibiotics and Antiviral Compounds. Chemical Synthesis and Modification,” eds. Krohn, K., Krist, H., and Maag, H. VCH, Weinheim, pp. 281-288 (1993).
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Isobe, M.1
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Synthetic studies on antibiotic dynemicin A. Synthesis of cyclic enediyne model compound of dynemicin A
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Nishikawa, T., Ino, A., and Isobe, M., Synthetic studies on antibiotic dynemicin A. Synthesis of cyclic enediyne model compound of dynemicin A. Tetrahedron, 50, 1449-1468 (1994).
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Nishikawa, T.1
Ino, A.2
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15
-
-
85011238572
-
-
have succeeded in the construction of 10-mem-bered enediyne by using double Stille coupling in their total synthesis of dynemicin A. See
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Danishefsky, D. et al. have succeeded in the construction of 10-mem-bered enediyne by using double Stille coupling in their total synthesis of dynemicin A. See
-
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Danishefsky, D.1
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16
-
-
0027991211
-
A Remarkable cross-coupling reaction to construct the enediyne linkage relevant to dynemicin A: Synthesis of the deprotected ABC system
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Shair, M. D., Yoon, T. Y., and Danishefsky, S. J., A Remarkable cross-coupling reaction to construct the enediyne linkage relevant to dynemicin A: Synthesis of the deprotected ABC system. J. Org. Chem., 59, 3755-3757 (1994).
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Shair, M.D.1
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Danishefsky, S.J.3
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17
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0030001543
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The total synthesis of dynemicin A leading to development of a fully contained bioreductively activated enediyne prodrug
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Shair, M. D., Yoon, T. Y., Mosny, K. K., Chou, T. C., and Danishefsky, S. J., The total synthesis of dynemicin A leading to development of a fully contained bioreductively activated enediyne prodrug. J. Am. Chem. Soc., 118, 9509-9525 (1996).
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18
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0002898647
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Tin (IV) acetylides. An overview
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Tributylstannyl(trimethylsilyl)ethyne (2) was prepared by the reaction of lithium trimethylsilylacetylide with tributyltin chloride. For a review on tinacetylene, see
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Cauletti, C.1
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19
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84989539773
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One-pot synthesis of haloacetylenes from trimethylsilylacetylenes
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Nishikawa, T., Shibuya S., Hosokawa, S., and Isobe, M., One-pot synthesis of haloacetylenes from trimethylsilylacetylenes. Synlett, 482-484 (1994).
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0001528735
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Palladium-catalyzed coupling of allylic acetates with aryl- and vinylstannanes
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Valle, L. D., Stille, J. K., and Hegedus, L. S., Palladium-catalyzed coupling of allylic acetates with aryl- and vinylstannanes. J. Org. Chem., 55, 3019-3023 (1990).
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Valle, L.D.1
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0000931564
-
New synthetic reactions of allyl alkyl carbonates, allyl β-keto carboxylates, and allyl vinylic carbonates catalyzed by palladium complexes
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For a review of allyl carbonates in Pd-catalyzed reactions, see
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For a review of allyl carbonates in Pd-catalyzed reactions, see: Tsuji, J., and Minami, I., New synthetic reactions of allyl alkyl carbonates, allyl β-keto carboxylates, and allyl vinylic carbonates catalyzed by palladium complexes. Acc. Chem. Res., 20, 140-145 (1987).
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Tsuji, J.1
Minami, I.2
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22
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0030565554
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Palladium-catalyzed cross-coupling reaction of allyl carbonates with organostannanes
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The coupling reaction of allyl carbonates with organotin compounds (aryl, vinyl) has recently been reported
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has recently been reported. Castano A. M. and Echavarren, A. M., Palladium-catalyzed cross-coupling reaction of allyl carbonates with organostannanes. Tetrahedron Lett., 37, 6587-6590 (1996).
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Castano, A.M.1
Echavarren, A.M.2
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23
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-
0000076362
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Novel dependency of stereochemistry upon metal, ligand, and solvent in oxidative addition of allylic chloride to Pd(0) and Pt(0) complexes
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This reaction condition was modified from Kurosawa’s conditions
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complexes. J. Am. Chem. Soc., 112, 2813-2814 (1990).
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Kurosawa, H.1
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Ikeda, I.6
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24
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0010399461
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Novel syn oxidative addition of allylic halides to olefin complexes of palladium(O) and platinum(O)
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and platinum(O). J. Am. Chem. Soc., 114, 8417-8424 (1992).
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Kurosawa, H.1
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Murai, S.7
Ikeda, I.8
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