Recent developments in syntheses of the post-secodine indole alkaloids. Part III: Rearranged alkaloid types

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F11%3A10132966" target="_blank" >RIV/00216208:11310/11:10132966 - isvavai.cz</a>
Result on the web
<a href="http://cccc.uochb.cas.cz/76/12/2023/" target="_blank" >http://cccc.uochb.cas.cz/76/12/2023/</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1135/cccc2011099" target="_blank" >10.1135/cccc2011099</a>

Result language
angličtina
Original language name
Recent developments in syntheses of the post-secodine indole alkaloids. Part III: Rearranged alkaloid types
Original language description
The third part of a planned review on developments in the field of total and formal total synthesis of the post-secodine indole alkaloids focuses on types of rearranged alkaloids, i.e. on the skeletons with altered connectivities next to the indol(e)inemoiety, especially with a new bond to N-1. It reviews the synthesis of melodane, goniomitine, chippiine/dippinine, lirofoline and tronocarpine alkaloids, as well as alkaloids of secoschizozygane/vallesamidine, schizozygane and isoschizozygane type. It covers the literature from approximately 1991 up to May 2011. A review with 115 references.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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