112424-06-3

Upstream product

• 17534-15-5 Benzene-1,2-dithiol 
• 39078-11-0 cis-trisoxirane 
• 39234-86-1 3,5-bis(trifluoromethyl)benzenesulfonyl chloride 
• 112424-03-0 (1α,2β,3β,4α,5α,6α)-5,6-Epoxy-2,3-S-(1,2-phenylen)-2,3-dithio-1,2,3,4-cyclohexantetrol 

Downstream Products

• 112424-09-6 DL-(1α,2α,3α,4α,5β,6β)-1,2:3,4-Bis-S-(1,2-phenylen)-1,2,3,4-tetrathio-1,2,3,4,5,6-cyclohexanhexol-5-<3,5-bis(trifluormethyl)benzolsulfonat> 
• 112424-11-0 DL-(1α,2α,3α,4α,5β,6β)-6-O-(Methylsulfonyl)-1,2:3,4-bis-S-(1,2-phenylen)-1,2,3,4-tetrathio-1,2,3,4,5,6-cyclohexanhexol-5-<3,5-bis(trifluormethyl)benzolsulfonat> 
• 112424-10-9 (1α,2α,3α,4α,5β,6β)-1,2:3,4-Bis-S-(1,2-phenylen)-1,2,3,4-tetrathio-1,2,3,4,5,6-cyclohexanhexol-5,6-bis-<3,5-bis(trifluormethyl)benzolsulfonat> 

Relevant academic research and scientific papers

cis-/trans--Trithia- and trans--Hexathia-tris-?-homobenzenes

Starting from the cis- and trans-benzene trioxides 2/7 the cis-/trans--Trithia-tris-?-homobenzenes 1/6 and the trans-dioxathia-/oxadithia analogs 19/21 are synthesized by regioselective epoxide opening reactions with appropriate S-nucleophiles.Under the influence of heat and light cis-trisulfide 1 quickly looses sulfur and does not undergo ?2+?2+?2>cycloreversion.Attempts to build up cis--tris-?-homobenzenes from 2 by threefold six-membered ring anellation, in the special case of 1,2-benzenedithiol as 1,4-dinucleophil, led preferably to the trans--hexathia-tris-?-homobenzene 44 (X-ray analysis) manifesting effective S-neighbouring group participation. cis-Trisulfide 1 is a poor tridentate ligand: only with Ni(ClO4)2 a 2:1 complex (presumably octahedral, 48) is formed.