Catalytic asymmetric synthesis of tetrahydrocarbazoles
Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The ad...
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| Published in | Chemical communications (Cambridge, England) Vol. 55; no. 44; pp. 6151 - 6164 |
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| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
England
Royal Society of Chemistry
28.05.2019
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The advent of asymmetric catalysis provides a powerful platform to assemble chiral THC motifs and great efforts have been devoted to this field over the past decades. In this feature article, we summarise recent advances in catalytic asymmetric synthesis of THCs, with particular emphases on reaction types and reaction mechanism.
This feature article summarises recent advances in catalytic asymmetric synthesis of THCs, with emphases on reaction type and reaction mechanism. |
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| AbstractList | Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The advent of asymmetric catalysis provides a powerful platform to assemble chiral THC motifs and great efforts have been devoted to this field over the past decades. In this feature article, we summarise recent advances in catalytic asymmetric synthesis of THCs, with particular emphases on reaction types and reaction mechanism.Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The advent of asymmetric catalysis provides a powerful platform to assemble chiral THC motifs and great efforts have been devoted to this field over the past decades. In this feature article, we summarise recent advances in catalytic asymmetric synthesis of THCs, with particular emphases on reaction types and reaction mechanism. Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The advent of asymmetric catalysis provides a powerful platform to assemble chiral THC motifs and great efforts have been devoted to this field over the past decades. In this feature article, we summarise recent advances in catalytic asymmetric synthesis of THCs, with particular emphases on reaction types and reaction mechanism. Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The advent of asymmetric catalysis provides a powerful platform to assemble chiral THC motifs and great efforts have been devoted to this field over the past decades. In this feature article, we summarise recent advances in catalytic asymmetric synthesis of THCs, with particular emphases on reaction types and reaction mechanism. This feature article summarises recent advances in catalytic asymmetric synthesis of THCs, with emphases on reaction type and reaction mechanism. |
| Author | Cheng, Hong-Gang Tan, Fen |
| AuthorAffiliation | Wuhan University College of Chemistry and Molecular Sciences Hubei Key Laboratory of Purification and Application of Plant Anti-cancer Active Ingredients Hubei University of Education |
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| Author_xml | – sequence: 1 givenname: Fen surname: Tan fullname: Tan, Fen – sequence: 2 givenname: Hong-Gang surname: Cheng fullname: Cheng, Hong-Gang |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31093637$$D View this record in MEDLINE/PubMed |
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| Notes | Hong-Gang Cheng was born in Jiangxi, P. R. China. He received his PhD degree under the supervision of Prof. Wen-Jing Xiao from Central China Normal University in 2014. Then he joined Prof. Sh Kobayashi's group as a postdoctoral fellow at the University of Tokyo and worked there for one year. Since February 2016, he has worked at Wuhan University. His research interest focuses on the development of new synthetic methodologies. Fen Tan was born in Hubei, P. R. China. She obtained her BSc degree from Dezhou University in 2008 and received her PhD degree in 2014 under the supervision of Prof. Wen-Jing Xiao at Central China Normal University. Since August 2014, she has worked at Hubei University of Education. Her research interests focus on asymmetric catalysis and green synthetic chemistry. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
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| Snippet | Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of... |
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| SubjectTerms | Alkaloids Alkylation Asymmetry bioactive properties Carbazoles - chemical synthesis Carbazoles - chemistry Catalysis catalytic activity chemical reactions Chemical synthesis Cycloaddition Reaction drugs indole alkaloids Indoles - chemistry Lewis Acids - chemistry Molecular Structure Reaction mechanisms Stereoisomerism stereoselective synthesis |
| Title | Catalytic asymmetric synthesis of tetrahydrocarbazoles |
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