Reversal of Selectivity in C3-Allylation and Formal [3 + 2]-Cycloaddition of Spiro-epoxyoxindole: Unified Synthesis of Spiro-furanooxindole, (±)-N-Methylcoerulescine, (±)-Physovenine, and 3a-Allylhexahydropyrrolo[2,3-b]indole-Reference-Cited by-同舟云学术

Reversal of Selectivity in C3-Allylation and Formal [3 + 2]-Cycloaddition of Spiro-epoxyoxindole: Unified Synthesis of Spiro-furanooxindole, (±)-N-Methylcoerulescine, (±)-Physovenine, and 3a-Allylhexahydropyrrolo[2,3-b]indole

Published:2017-04-06 Issue:8 Volume:19 Page:1998-2001
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hajra Saumen¹^ORCID,Roy Sayan¹,Maity Subrata¹²

Affiliation:

1. Centre of Biomedical Research, Sanjay Gandhi Post-Graduate Institute of Medical Sciences Campus, Raebareli Road, Lucknow 226014, India

2. Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302, India

Funder

Council of Scientific and Industrial Research

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b00420

Reference41 articles.

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2. bAnthoni, U.; Christophersen, C.; Nielsen, P. H.InAlkaloids: Chemical and Biological Perspectives;Pelletier, S. W., Ed.Pergamon:London, 1999; Vol.13, pp163–236.

3. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit (1999)

4. BMS-204352: A Potassium Channel Opener Developed for the Treatment of Stroke

5. Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters: Synthetic and Mechanistic Studies of the C-Acylation of Silyl Ketene Acetals

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