77128-57-5Relevant academic research and scientific papers
PHOTOCHEMICAL RING CLOSURE OF α,α-BISULFENYLATED CARBONYL COMPOUNDS STEREOSELECTIVE FORMATION OF CIS-DIHYDROBENZOTHIOPHENES
Sasaki, Tadashi,Hayakawa, Kenji,Nishida, Sumio
, p. 75 - 83 (2007/10/02)
Photochemistry of α,α-bisulfenylated ketone has been investigated.Irradiation of 2-phenylthiodihydrothiophen-3-one (1) in benzene gave the radical recombination products 9 (63percent) and 10 (49percent).In a polar solvent, the ionic chemistry became predominant.Brief irradiation of 1 in acetonitrile and methanol gave the cis-fused dihydrothiophene 11 as the major product in 43percent and 20percent yields, respectively.The stereoselective photocyclization was generally observed for other ketones (2-8) in acetonitrile solution (Table 1).The photoproducts were easily dehydrated by treating with boron trifluoride etherate to give the corresponding benzothiophenes in high yields.Simple α-phenylthioketones are photoinert under the same conditions.The mechanism of this novel photocyclization of bisulfenylated ketones is also discussed.
-SIGMATROPIC REARRANGEMENT OF ALLYL 2-BENZOTHIENYL SULFIDE
Anisimov, A. V.,Babaitsev, V. S.,Grobovenko, S. Ya.,Danilova, T. A.,Viktorova, E. A.
, p. 447 - 450 (2007/10/02)
Allyl 2-benzothienyl sulfide at 20-120 deg C undergoes a -sigmatropic rearrangement to give 3-allylbenzothiophene-2-thiol.The kinetic parameters of the reaction were studied.Under the experimental conditions the thiol undergoes cyclization to give 2-methyl-2,3-dihydrobenzothienothiophene, 2-methylbenzothienothiophene, and benzothienodihydrothiopyran.Allyl 3-methyl-2-benzothienyl sulfide does not form a thiol even at 150-190 deg C but rather forms only bis(3-methyl-2-benzothienyl) disulfide.
