| 2. |
- Shirani, Hamid
(författare)
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Application of metalation reactions for synthesis of sulfur/selenium-containing heterocyclic compounds
- 2009
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- This thesis deals mainly with the synthesis of various sulfur/selenium-containing heterocyclic compounds, many of which include structural features present in several biologically active molecules, with particular emphasis on compounds of synthetic importance, such as indoles, as well as other heteroaromatic species. In the first part, an efficient procedure toward synthesis of new 3-(arylthio)indoles based on reactions of aryl Grignard reagents or lithiated heteroaromatics with protected 3,3′-dithiobisindoles is described. In addition, the heterocyclic core of the marine alkaloid echinosulfone A, namely 3,3′-bis(indolyl) sulfone, was obtained by treatment of a 3-lithioindole derivative with bis(phenylsulfonyl) sulfide. These methodologies offer convenient synthetic routes toward a wide range of 3-(arylthio)indoles in good yields. In an extension, the sulfonation of 1-(phenylsulfonyl)indoles and pyrroles using chlorosulfonic acid in acetonitrile has been studied, leading to development of a simple and clean protocol for synthesis of the corresponding 1-phenylsulfonyl-1H-indole-3-sulfonyl chlorides and 1-phenylsulfonyl-1H-pyrrole-3-sulfonyl chlorides. In the second part, a new practical approach is described toward the synthesis of several biologically active indolothiopyrans and related selenopyrans, as analogues of indolocarbazoles. The target compounds were accessed via treatment of C-2 metalated indoles with bis(phenylsulfonyl) sulfide or selenide, followed by cyclization of the intermediate 2,2′-di(indolyl) sulfide/selenides, involving for example triethyl orthoformate under acidic conditions. The final section of this thesis describes a new method for synthesis of dibenzo[b,f]thiepins and related fused systems via ortho-metalation of aromatic acetals, followed by treatment with bis(phenylsulfonyl) sulfide, initially giving symmetrical diaryl-sulfides, which were subjected to deacetalization, and finally McMurry coupling. The method could also be extended to preparation of thiepin analogues such as 1-sila-, 1-germa- and 1-selenacyclohepta-2,4,6-trienes containing two fused aromatic or heterocyclic units.
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| 3. |
- Shirani, Hamid, et al.
(författare)
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New routes to 3-(Arylthio)indoles : Application to the synthesis of the 3,3 '-bis(indolyl) sulfone core of the marine alkaloid echinosulfone A
- 2006
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Ingår i: Synlett. - : Georg Thieme Verlag KG. - 0936-5214 .- 1437-2096. ; :15, s. 2459-2463
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Tidskriftsartikel (refereegranskat)abstract
- A new approach to 3-(arylthio)indoles and related compounds has been developed, based on the reactions of aryl Grignard reagents or lithiated heteroaroinatics with a phenylsulfonyl-protected 3,3'-bis(indolyl) disulfide. In addition, a rational approach to the 3,3'-bis(indolyl) sulfone core of the alkaloid echinosulfone A has been accomplished, involving treatment of a 3-lithioindole with bis(phenylsulfonyl) sulfide as the key step.
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