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PREPARATION OF ETHERS, EPOXIDES AND THIOETHERS

ETHERS, EPOXIDES, AND THIOETHERS FROM ACID DERIVATIVES [Pg.325]

Harkal, S. Kumar, K. Michalik, D. Zapf, A. Jackstell, R. Rataboul, F. Riermeier, T. Monsees, A. Beller, M. Tetrahedron Lett. 2005, 46, 3237. [Pg.329]

Nishibayashi, Y. Milton, M.D. Inada, Y. Yoshikawa, M. Wakiji, I. Hidai, M. Uemura, S. [Pg.329]

5% Ir-complex, toluene 20% 1 -phenyl-1 -propyne, K3PO4, rt, 22h pj  [Pg.331]

SECTION 129 ETHERS, EPOXIDES, AND THIOETHERS FROM ETHERS, EPOXIDES, AND THIOETHERS [Pg.332]

SECTION 121 ETHERS, EPOXIDES AND THIOETHERS FROM ALKYNES [Pg.188]

Sansoulet, J. Dlez-Bana, E. Carrillo. J.R. Synth. Conunun., 1991, 21, 1465. [Pg.185]

SECTION 121 Ethers, Epoxides, and Thioethers from Acetylenes [Pg.164]

J Evans Jr., S.A. J Org Chan, (1986), 51, 5490 SECTION 124 Ethers, Epoxides, and Thioethers from Aldehydes CHO [Pg.167]

SECTION 125 Ethers, Epoxides, Thioethers from Alkyls, Methylenes, and Aryls [Pg.168]

Miniere, S. Reboul. V. Metzner.P. Fochi, M. Bonini, B.F. Tetrahedron Asymmetry 2004,15, 3275. [Pg.231]

Ootsuka, K. Suda, S. Nishikari, H. Hosomi. A. Synlett 2002,313. [Pg.231]

Nagayama, S. Mizutani, K. Hiori, R. Miyoshi, N. Chem. Lett. 2002,248. [Pg.231]

Zolfigol. M.A. Mohammadpor-Baltork, I. Habibi.D. Mirjalili, B.F. Bamoniri, A. Tetrahedron Lett. 2003, 44, 8165. [Pg.233]

Nakavama. J. Takahashi, K. Watanabe, T. Sugihara, Y. Ishii, A. Tetrahedron Lett., 2000, 41, 8349. [Pg.335]

Hirano, T. Kitano, Y. Tada, M. Chem. Commun., 1999, 691. [Pg.338]

DMBQ = 2,6-dimethyl-l,4-benzoquinone Shintou, T. Kikuchi, W. Mukaiyama, T. Chem. Lett. 2003,32,22. ClPPh, [Pg.229]

Fischer, S. Groth.U. Jeske, M. Schiltz, T. Synlett2002,1922. BiCk, Eton, EtjSiH [Pg.231]

The preparation of novel triazole-containing 20-22 membered macrocyclic azacrown ether-thioethers was reported <96JCR(S)182> and the first selective synthetic method fra the synthesis of dicyanotriazolehemiporhyrazines was published <96JOC6446>. 1,2,4-Triazole-containing polyimide beads were prepared and employed as Mo(VI) epoxidation catalyst supports, liie 1,2,4-nitronyl nitroxide 29 was also synthesized and found to have remarkable magnetic properties <96AM60>. [Pg.163]

See other pages where PREPARATION OF ETHERS, EPOXIDES AND THIOETHERS is mentioned: [Pg.156]    [Pg.19]    [Pg.164]    [Pg.156]    [Pg.227]    [Pg.335]    [Pg.127]    [Pg.127]    [Pg.188]    [Pg.325]    [Pg.156]    [Pg.184]    [Pg.227]    [Pg.156]    [Pg.19]    [Pg.164]    [Pg.156]    [Pg.227]    [Pg.335]    [Pg.127]    [Pg.127]    [Pg.188]    [Pg.325]    [Pg.156]    [Pg.184]    [Pg.227]    [Pg.17]    [Pg.17]    [Pg.590]    [Pg.816]    [Pg.683]    [Pg.730]    [Pg.16]    [Pg.188]    [Pg.12]    [Pg.14]   


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Epoxides preparation

Epoxides thioethers

Ethere preparation

Ethers and Epoxides

Ethers preparation

Ethers thioethers

Of thioethers

Preparation of Thioethers

Preparing Ethers

Thioether epoxides

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