Synthesis of indole alkaloid analogues: Novel domino stereoselective electrophile addition - Cyclizations of tryptophan-derived α-amino nitriles
Journal of Organic Chemistry, ISSN: 0022-3263, Vol: 72, Issue: 14, Page: 5395-5398
2007
- 16Citations
- 10Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations16
- Citation Indexes16
- 16
- CrossRef13
- Captures10
- Readers10
- 10
Article Description
(Chemical Equation Presented) The synthesis of new indole alkaloid analogues, containing a 1,2,4,5,10b,10c-hexahy dropyrrolo[1′,2′, 3′:1,9a,9]imidazo-[1,2-a]indole skeleton, via highly stereoselective novel domino cyclative halogenation or prenylation reactions of tryptophan-derived α-amino nitriles, is described. © 2007 American Chemical Society.
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