共查询到20条相似文献,搜索用时 500 毫秒
1.
Qi Qin Xin-Lian Liu Dr. Ai-Jun Ma Dr. Xiang-Zhi Zhang Prof. Dr. Jin-Bao Peng 《化学:亚洲杂志》2021,16(23):3890-3894
An efficient method for the stereoselective synthesis of (Z)-3-((arylamino)methylene)indoline-2-thiones have been developed via a novel multicomponent reaction of indoles, CS2 and nitroarenes. A range of functionalized indoline-2-thiones were prepared in moderate to good yields from easily available starting materials. The indoline-2-thione products can be easily derivatized to give biologically active thieno[2,3-b]indole and thiopyrano[2,3-b]indole skeletons in high yields. 相似文献
2.
《Tetrahedron letters》2014,55(51):7043-7046
A facile synthesis of indole annulated 2H-thiopyran-2-ones has been developed by condensation of indoline-2-thiones with acetoacetic esters in the presence of borontrifluoride etherate (BF3 etherate) using microwave irradiation. This one-step operationally simple methodology leads to thiopyrano[2,3-b]indol-2-ones in good yields. 相似文献
3.
The photochemical synthesis of indole derivatives starting from the indoline-2-thiones 1 is described. Irradiation of indoline-2-thiones 1 in the presence of alkenes 3 gave 2-alkyl-3H-indoles 4 – 7 or 2-alkylindoles 8 – 22 through the ring cleavage of the intermediates, spirocyclic amino-thietanes, initially derived by [2 + 2] cycloaddition of the C?S bond of 1 and the C?C bond of 3 . Irradiation of 1 in the presence of trialkylamines 26 gave desulfurization products 27 – 32 and unexpected 3-alkylindoles 33 – 40 . N-Acylindoline-2-thiones 11 - p yielded the deacylated products, indoline-2-thiones 1a - b , and ethyl esters 43 through γ-H abstraction by the excited thioamide S-atom when irradiated in CDC13/EtOH or benzene/EtOH. Oxygen analogues 2a - d also underwent intramolecular H abstraction to give the indolin-2-ones 2e – f and ethyl esters 43 in a similar way. 相似文献
4.
An efficient method for the synthesis of thiazolidine-2-thiones is described via regiospecific iodocyclization of an allyl amine, carbon disulfide, and iodine. Dehydrohalogenation of the iodo-derivatives gives thiazole-2(3H)-thiones. In addition, nucleophilic substitution of the iodine in the products is accomplished using NaN3, thiophenol, or dithiocarbamate. 相似文献
5.
Zhen LiLongcheng Hong Ruiting LiuJianzhong Shen Xigeng Zhou 《Tetrahedron letters》2011,52(12):1343-1347
The copper-catalyzed chalcogenoamination of 2-alkynylanilines with dichalcogenides has been achieved under mild reaction conditions using the weak base Cs2CO3 in combination with air oxidant, providing a convenient and efficient method for synthesis of 3-sulfenylindoles and 3-selenylindoles, including complex products bearing two attached 3-sulfenylindole rings. 相似文献
6.
Salman Taheri Ali Asghar Mohammadi Reza Ahdenov Robab Azarlak 《Journal of the Iranian Chemical Society》2016,13(7):1301-1306
An efficient one-pot synthesis of fused dihydrothiopyrano[2,3-b]indole-3-carbonitriles has been developed through ultrasound mediated reaction by simply combining malononitrile and various aldehydes with two indoline-2(3H)-thiones. The method has the advantages of high yields, short reaction time, good functional group tolerance and green reaction conditions. 相似文献
7.
Reduction of indolin-2-ones with lithium aluminium hydride (LAH) or diisobutylaluminum hydride (DIBAL) and desulfurization of indoline-2-thiones with Raney-Ni were investigated. Treatment of indoline-2-ones 1 with LAH or DIBAL yield indoles 4 and/or indolines 3 in moderate-to high yield depending on the substituents at N and C(3) of 1 . Indoline-2-thiones 2 were desulfurized with Raney-Ni to give indoles 4 and/or indolines 3 . 相似文献
8.
A versatile synthesis of symmetrically and unsymmetrically substituted thiopyrano[2,3-b:6,5-b′]diindoles has been developed by the condensation of 2-(alkylthio)-indole-3-carbaldehydes with indoline-2-thiones in the presence of catalytic amount of ethylenediamine diacetate (EDDA). The EDDA mediated condensation leads to a spontaneous cyclization followed by aromatization to form thiopyrano[2,3-b:6,5-b′]diindoles in quantitative yields. 相似文献
9.
Frank Hochberger-Roa Perla H. García-Ríos Jos G. Lpez-Corts M. Carmen Ortega-Alfaro Jean-Claude Daran Maryse Gouygou Martine Urrutigoïty 《Molecules (Basel, Switzerland)》2022,27(3)
A new synthetic alternative to the synthesis of 3-methyl indoles and 3-methyl indoline-2-ols with an excellent atomic economy is presented in this study. It is demonstrated that the intramolecular interrupted hydroaminomethylation (HAM) reaction is a powerful tool for the formation of these compounds, which exhibit wide-ranging biological activity. Several N-Protected-2-vinyl anilines were synthesized and involved in the reaction producing the corresponding 3-methylindole or 3-methyl indoline-2-ol depending on the nature of the N-protecting groups. 相似文献
10.
A. D. Shutalev E. N. Komarova L. A. Ignatova 《Chemistry of Heterocyclic Compounds》1993,29(10):1182-1191
A convenient method for the synthesis of hexahydropyrimidine-2-thiones by the reduction of the readily accessible 4-hydroxy(alkoxy)hexahydropyrimidine-2-thiones and 1,2,3,6-tetrahydropyrimidine-2-thiones by the NaBH4-CF3COOH system was proposed.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1378–1388, October, 1993. 相似文献
11.
A nucleophile-catalyzed Michael addition/proton transfer/lactonization (NCMPL) organocascade process of chiral α,β-unsaturated acylammonium salts and indoline-2-thiones is described, which delivers the indolo[2,3-b]dihydrothiopyranone motifs in high yields (up to 97%) with good to excellent enantioselectivities (up to 98% ee). 相似文献
12.
Mrityunjaya Asthana Neha SharmaRitush Kumar Jay Bahadur SinghRadhey M. Singh 《Tetrahedron letters》2014
I2-catalyzed base-free reactions of 3-homoallylquinoline-2-thiones have been described for the synthesis of tetracyclic quinolines, tetrahydrofuro [2′,4′:4,6]thiopyrano[2,3-b]quinolines in excellent yields. Similarly, I2-catalyzed reactions could proceed to tricyclic quinolines from hydroxyl group protected 3-homoallylquinoline-2-thiones. However, deprotection of group in tricyclic quinoline with HI again transformed into tetracyclic quinoline. The sulfonium salt intermediate has been proposed to explain these reactions. 相似文献
13.
Rajiv Kumar VermaGirijesh K. Verma Keshav RaghuvanshiMaya Shankar Singh 《Tetrahedron》2011,67(3):584-589
A convenient and one-pot synthesis of 3-aroyl/heteroaroyl-2H-chromene-2-thiones and benzo[f]2H-chromene-2-thiones has been developed by the condensation of β-oxodithioesters and salicylaldehydes/α-hydroxynaphthaldehydes in the presence of indium trichloride under solvent-free conditions. The reaction is operationally facile, readily scalable, and offers rapid entry into differentially substituted chromene-2-thione scaffolds. 相似文献
14.
Alkyl and acyl derivatives of 3,4-dihydropyrimidin-2(1H)-thiones were synthesized in good to excellent yields in the presence of Cs2CO3, a mild base. The method evidences a selective S-alkylation when using acyl chlorides as efficient acylating agents at room temperature on the 2-thioxo-dihydropyrimidone moiety. A possible mechanistic interpretation of the different selectivities in case of alkylation and acylation was done with the help of a geometry optimization process. 相似文献
15.
Vladimir V. Kouznetsov Josué S. Bello Forero Diego F. Amado Torres 《Tetrahedron letters》2008,49(41):5855-5857
An easy, fast, and cheap way for the synthesis of the new 4′-(4-hydroxy-3-methoxyphenyl)-3′-methyl-3′,4′-dihydro-1′H-spiro[indoline-3,2′-quinolin]-2-ones using BF3 OEt2-promoted imino Diels-Alder cycloaddition between ketimine-isatin derivatives and trans-isoeugenol. 相似文献
16.
A reaction method is described for selective reductive cleavage of 2-(phenylthio)pyrimidines using Pd(OAc)2 and Et3SiH to produce 2-(H)pyrimidines. The reaction proceeds efficiently with a wide range of 2-(phenylthio)pyrimidines. Considering the ready availability of 2-(arylthio)pyrimidines derived from oxidative CS cross coupling of 3,4-dihydropyrimidin-1H-2-thiones (DHPMs), this method unambiguously provides a shortcut to the preparation of 2-(H)pyrimidines with unprecedented diversity. 相似文献
17.
A. N. Kravchenko V. V. Baranov Yu. V. Nelyubina G. A. Gazieva I. V. Svitan’ko 《Russian Chemical Bulletin》2012,61(1):64-73
Studies on the synthesis of 4,5-dihydroxyimidazolidin-2-ones (-thiones) based on the condensation of ureas or thioureas with glyoxal or 1,2-dioxo-1,2-diphenylethane showed high diastereoselectivity in the formation of racemates (trans-diastereomers) of 4,5-dihydroxyimidazolidin-2-ones (-thiones) and meso-forms (cis-diastereomers) of 4,5-dihydroxy-4,5-diphenyl-1,3-dialkylimidazolidine-2-thiones; plausible mechanisms of their formation were suggested. X-ray diffraction studies confirmed structures of diastereomers for separate examples of racemates and meso-forms of 4,5-dihydroxyimidazolidin-2-ones (-thiones). 相似文献
18.
L. A. Rodinovskaya A. E. Fedorov A. M. Shestopalov P. A. Belyakov K. G. Nikishin 《Russian Chemical Bulletin》2013,62(10):2214-2226
A simple and convenient preparative method for the synthesis of 3-cyano-4-difluoro- and -trifluoromethylpyridine-2(1H)-thiones was developed. During studies of synthetic potential of these compounds, approaches to the synthesis of a number of annulated heterocyclic systems were suggested. 相似文献
19.
An easy, efficient, and simple one-pot approach for the synthesis of 1,3-thiazolidine-2-thiones via multicomponent reaction is reported. The reaction of a primary amine with carbon disulfide in the presence of dibenzoylacetylene or bis(4-methyl-1-benzoyl)acetylene in a mixture of CH2Cl2 and H2O after 5 h, afforded the title compound as alkene diastereomers. 相似文献
20.
B. V. Lichitsky R. M. Belyi A. N. Komogortsev A. A. Dudinov M. M. Krayushkin 《Russian Chemical Bulletin》2013,62(4):1026-1031
A method for the synthesis of 2,5′-dioxo-3′-phenyl-5′,6′-dihydro-4′H-spiro[indoline-3,7′-thieno[3,2-b]pyridine]-2′-carboxylic acids was elaborated based on the three-component condensation of 3-aminothiophenes, Meldrum’s acid, and isatines. 相似文献