Simple exploration of Sulfonyldibenzene

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 127-63-9. Category: isothiazole.

Chemistry, like all the natural sciences, Category: isothiazole, begins with the direct observation of nature¡ª in this case, of matter.127-63-9, Name is Sulfonyldibenzene, SMILES is O=S(C1=CC=CC=C1)(C2=CC=CC=C2)=O, belongs to isothiazole compound. In a document, author is Stachel, HD, introduce the new discover.

Fused 1,2-dithioles – Part VII – Synthesis and reactions of 4H-1,2-dithiolo[4,3-c]isothiazoles

The 1,2-dithiolosultam derivative 14 was obtained from the (alpha-bromoalkylidene)propenesultam derivative 9 (Scheme 1). Regioselective cleavage of the two ester groups ( -> 1b or 2b) allowed the preparation of derivatives with different substituents at C(3) in the dithiole ring (see 27 and 28) as well as at C(6) in the isothiazole ring (see 17 – 21; Scheme 2). Curtitis rearrangement of the 6-carbonyl azide 21 in Ac2O afforded the 6-acetamide 22, and saponification and decarboxylation of the latter yielded ‘sulfothiolutin’ (30). Hydride reductions of two of the bicyclic sultams resulted in ring opening of the sultam ring and loss of the sulfonyl group. Thus the reduction of the dithiolosultam derivative 14 yielded the alkylidenethiotetronic acid derivative 33 (tetronic acid = furan-2,4(3H,4H)-dione), and the lactam-sultam derivative 10 gave the alkylidenctetramic acid derivative 35 (tetramic acid= 1,5-dihvdro-4-hydroxy-2H-pyrrol-2-one) (Scheme 3). Some of the new compounds (14, 22, 26, and 30) exhibited antimycobacterial activity. The oxidative addition of 1 equiv. of [pt(eta(2)-C2H4)L-2] (36a, L – PPh3; 36b, L = 1/2 dppf; 36c, L = 1/2 (R,R)-diop) into the S-S bond of 14 led to the cis(dithiolato)platinum(II) complexes 37a-c. (dppf=1,1′-bis(diphenylphosphino)ferrocene; (R,R)-diop([(4R,5R)-2,2-demithyl-1,3-dioxolane-4,5-diyl]bis(iiiethylene)bis(diphenylphosphine]).

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 127-63-9. Category: isothiazole.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com