New Advances in Chemical Research in 2021, Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media. 127-63-9, Name is Sulfonyldibenzene, molecular formula is C12H10O2S, belongs to isothiazole compound. In a document, author is Stachel, HD, introduce the new discover, Quality Control of Sulfonyldibenzene.
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]).
Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. If you are hungry for even more, make sure to check my other article about 127-63-9, Quality Control of Sulfonyldibenzene.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com