Regioselective and Stereoselective Reductive Aziridinium Ring Cleavage Leading to Azabicyclodecane Architecture: Enantioselective Synthesis of (+)-Subincanadine F-Reference-Cited by-同舟云学术

Regioselective and Stereoselective Reductive Aziridinium Ring Cleavage Leading to Azabicyclodecane Architecture: Enantioselective Synthesis of (+)-Subincanadine F

Published:2018-08-30 Issue:19 Volume:83 Page:12164-12170
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kalshetti Manojkumar G.¹²,Argade Narshinha P.¹²^ORCID

Affiliation:

1. Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India

2. Academy of Scientific and Innovative Research (AcSIR), New Delhi 110 025, India

Funder

Council of Scientific and Industrial Research

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b02113

Reference52 articles.

1. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

2. Occurrence, Biogenesis, and Synthesis of Biologically Active Carbazole Alkaloids

3. Marine Indole Alkaloids

4. Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi

5. Subincanadines A−C, Novel Quaternary Indole Alkaloids from Aspidosperma subincanum

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