The Experts below are selected from a list of 177 Experts worldwide ranked by ideXlab platform
Erik V. Van Der Eycken - One of the best experts on this subject based on the ideXlab platform.
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Gold(I)-Catalyzed Post-Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles.
ChemInform, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:An efficient intramolecular hydroarylation reaction to the corresponding title heterocycles under mild reaction conditions is developed.
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Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones
Synthesis, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A post-Ugi late-transition-metal-catalyzed intramolecular hydroarylation approach opens a new gateway for the synthesis of diversely substituted pyrrolopyridinones, pyrroloazepinones thiophenoazepinones, Azepinoindoles, and azepinobenzothiophenes applying mild reaction conditions. A detailed investigation of the scope of this strategy is discussed.
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Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles
European Journal of Organic Chemistry, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A diversity-oriented approach comprising a Ugi four-component reaction and gold(I)-catalyzed hydroarylation under very mild reaction conditions has been elaborated. This gives direct access to the synthesis of biologically important heterocycles such as pyrrolopyridines, pyridoindoles, and Azepinoindoles in very good yields. The influence of the nucleophilicity of the heterocycle and the mode of ring closure are discussed.
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synthesis of the Azepinoindole framework via oxidative heck fujiwara moritani cyclization
ChemInform, 2011Co-Authors: Pavel A. Donets, Erik V. Van Der EyckenAbstract:The cyclization of 3-indoleacetic amides provides Azepinoindole derivatives in moderate yields.
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Synthesis of the Azepinoindole Framework via Oxidative Heck (Fujiwara—Moritani) Cyclization.
ChemInform, 2011Co-Authors: Pavel A. Donets, Erik V. Van Der EyckenAbstract:The cyclization of 3-indoleacetic amides provides Azepinoindole derivatives in moderate yields.
Amit Kumar - One of the best experts on this subject based on the ideXlab platform.
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Gold(I)-Catalyzed Post-Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles.
ChemInform, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:An efficient intramolecular hydroarylation reaction to the corresponding title heterocycles under mild reaction conditions is developed.
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Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones
Synthesis, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A post-Ugi late-transition-metal-catalyzed intramolecular hydroarylation approach opens a new gateway for the synthesis of diversely substituted pyrrolopyridinones, pyrroloazepinones thiophenoazepinones, Azepinoindoles, and azepinobenzothiophenes applying mild reaction conditions. A detailed investigation of the scope of this strategy is discussed.
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Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles
European Journal of Organic Chemistry, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A diversity-oriented approach comprising a Ugi four-component reaction and gold(I)-catalyzed hydroarylation under very mild reaction conditions has been elaborated. This gives direct access to the synthesis of biologically important heterocycles such as pyrrolopyridines, pyridoindoles, and Azepinoindoles in very good yields. The influence of the nucleophilicity of the heterocycle and the mode of ring closure are discussed.
Virinder S. Parmar - One of the best experts on this subject based on the ideXlab platform.
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Gold(I)-Catalyzed Post-Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles.
ChemInform, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:An efficient intramolecular hydroarylation reaction to the corresponding title heterocycles under mild reaction conditions is developed.
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Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones
Synthesis, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A post-Ugi late-transition-metal-catalyzed intramolecular hydroarylation approach opens a new gateway for the synthesis of diversely substituted pyrrolopyridinones, pyrroloazepinones thiophenoazepinones, Azepinoindoles, and azepinobenzothiophenes applying mild reaction conditions. A detailed investigation of the scope of this strategy is discussed.
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Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles
European Journal of Organic Chemistry, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A diversity-oriented approach comprising a Ugi four-component reaction and gold(I)-catalyzed hydroarylation under very mild reaction conditions has been elaborated. This gives direct access to the synthesis of biologically important heterocycles such as pyrrolopyridines, pyridoindoles, and Azepinoindoles in very good yields. The influence of the nucleophilicity of the heterocycle and the mode of ring closure are discussed.
Sunil K. Sharma - One of the best experts on this subject based on the ideXlab platform.
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Gold(I)-Catalyzed Post-Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles.
ChemInform, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:An efficient intramolecular hydroarylation reaction to the corresponding title heterocycles under mild reaction conditions is developed.
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Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones
Synthesis, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A post-Ugi late-transition-metal-catalyzed intramolecular hydroarylation approach opens a new gateway for the synthesis of diversely substituted pyrrolopyridinones, pyrroloazepinones thiophenoazepinones, Azepinoindoles, and azepinobenzothiophenes applying mild reaction conditions. A detailed investigation of the scope of this strategy is discussed.
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Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles
European Journal of Organic Chemistry, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A diversity-oriented approach comprising a Ugi four-component reaction and gold(I)-catalyzed hydroarylation under very mild reaction conditions has been elaborated. This gives direct access to the synthesis of biologically important heterocycles such as pyrrolopyridines, pyridoindoles, and Azepinoindoles in very good yields. The influence of the nucleophilicity of the heterocycle and the mode of ring closure are discussed.
Dipak D. Vachhani - One of the best experts on this subject based on the ideXlab platform.
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Gold(I)-Catalyzed Post-Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles.
ChemInform, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:An efficient intramolecular hydroarylation reaction to the corresponding title heterocycles under mild reaction conditions is developed.
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Post Ugi Gold(I)- and Platinum(II)-Catalyzed Alkyne Activation: Synthesis of Diversely Substituted Fused Azepinones and Pyridinones
Synthesis, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A post-Ugi late-transition-metal-catalyzed intramolecular hydroarylation approach opens a new gateway for the synthesis of diversely substituted pyrrolopyridinones, pyrroloazepinones thiophenoazepinones, Azepinoindoles, and azepinobenzothiophenes applying mild reaction conditions. A detailed investigation of the scope of this strategy is discussed.
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Gold(I)‐Catalyzed Post‐Ugi Hydroarylation: An Approach to Pyrrolopyridines and Azepinoindoles
European Journal of Organic Chemistry, 2013Co-Authors: Amit Kumar, Dipak D. Vachhani, Sachin G. Modha, Sunil K. Sharma, Virinder S. Parmar, Erik V. Van Der EyckenAbstract:A diversity-oriented approach comprising a Ugi four-component reaction and gold(I)-catalyzed hydroarylation under very mild reaction conditions has been elaborated. This gives direct access to the synthesis of biologically important heterocycles such as pyrrolopyridines, pyridoindoles, and Azepinoindoles in very good yields. The influence of the nucleophilicity of the heterocycle and the mode of ring closure are discussed.
