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Cyclododecane, 1,5,9-trithia

S3BHKN6C12H15, Borate(l-), hydrotris(methi-mazolyl)-, potassium, 33 200 SsCgHig, Cyclododecane, 1,5,9-trithia-, 33 120 S3CrOi5C2iH33, Chromium(III), hexaaqua-, tris(p-toluenesulfonate), 33 97 S3EUF9N8O14C24H34, Europium(lll), l-(4-nitro-benzyl)-4,7,10-tris(carbamoyhnethyl)-1,4,7,10-tetraazacyclododecane-, 33 217 S3Fe09C2iH2i, Iron(III), tris(p-toluene-sulfonate), 33 99... [Pg.273]

For instance, thiacyclobutane, or thietane, can be trimerized into 1,5,9-trithia-cyclododecane in the presence of [Re3( -H)3(w-SCH2CH2CH2)(CO)io] which itself results from the reaction of thietane with [Re3(M-H)3CO)io(NCMe)2]. A simplified catalytic cycle is shown in Scheme 2, where the vertex represents rhenium atoms (bridging hydrides and terminal CO ligands have been omitted for clarity). [Pg.848]

C9H18S3, Cyclododecane, l,5,9-trithia-, 33 120 C11H9NO3, Hydroxamic acid, 3-hydroxy-2-naphtho-, 33 72... [Pg.257]


See also in sourсe #XX -- [ Pg.33 , Pg.120 ]




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