Synthetic Studies toward 1,2,3,3a,4,8b-Hexahydropyrrolo[3,2-<i>b</i>]indole Core. Unusual Fragmentation with 1,2-Aryl Shift-Reference-Cited by-同舟云学术

Synthetic Studies toward 1,2,3,3a,4,8b-Hexahydropyrrolo[3,2-b]indole Core. Unusual Fragmentation with 1,2-Aryl Shift

Published:2022-01-06 Issue:2 Volume:87 Page:1434-1444
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Aksenov Alexander V.¹^ORCID,Aleksandrova Elena V.¹^ORCID,Aksenov Dmitrii A.¹,Aksenova Anna A.¹,Aksenov Nicolai A.¹,Nobi Mezvah A.²,Rubin Michael¹²^ORCID

Affiliation:

1. Department of Chemistry, North Caucasus Federal University, 1a Pushkin St., Stavropol 355009, Russian Federation

2. Department of Chemistry, University of Kansas, 1567 Irving Hill Road, Lawrence, Kansas 66045, United States

Funder

Russian Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02753

Reference22 articles.

1. Inhibition on cholinesterase and tyrosinase by alkaloids and phenolics from Aristotelia chilensis leaves

2. Chemical study and anti-inflammatory, analgesic and antioxidant activities of the leaves of Aristotelia chilensis (Mol.) Stuntz, Elaeocarpaceae

3. Alkaloids Purified from Aristotelia chilensis Inhibit the Human α3β4 Nicotinic Acetylcholine Receptor with Higher Potencies Compared with the Human α4β2 and α7 Subtypes

4. Synthesis of Isoindoles by One-Electron Reductions of Dibenzo[1,4]diazocines

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