Alkoxylation Followed by Iodination of Oxindole with Alcohols Mediated by Hypervalent Iodine Reagent in the Presence of Iodine-Reference-Cited by-同舟云学术

Alkoxylation Followed by Iodination of Oxindole with Alcohols Mediated by Hypervalent Iodine Reagent in the Presence of Iodine

Published:2018-08-17 Issue:33 Volume:2018 Page:4556-4564
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Kotagiri Rajendraprasad¹²^ORCID,Adepu Ramesh³

Affiliation:

1. College of Pharmacy; Jinan University; No. 601 Huangpu Avenue West 510632 Guangzhou China

2. Inorganic and Physical Chemistry Division; CSIR-Indian Institute of Chemical Technology; Uppal Road, Tarnaka 500 007 Hyderabad Telangana State India

3. Organic and Biomolecular Chemistry Division; CSIR-Indian Institute of Chemical Technology; 500 007 Hyderabad India

Funder

Jinan University

indian institute of chemical technology

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201800723/fullpdf

Reference52 articles.

1. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

3. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

4. Natürliche Pyrrolidinylspirooxindole als Vorlagen für die Entwicklung medizinischer Wirkstoffe

5. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

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