Towards a Step-Economical and Waste-Free [hmim]Br-Catalyzed Deprotection of β-Sulfido Carbonyl Groups into (E )-Enones and Mechanistic Insights-Reference-Cited by-同舟云学术

Towards a Step-Economical and Waste-Free [hmim]Br-Catalyzed Deprotection of β-Sulfido Carbonyl Groups into (E )-Enones and Mechanistic Insights

Published:2017-11-02 Issue:12 Volume:6 Page:1867-1875
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Thopate Yogesh¹²,Singh Richa¹,Sharma Tanuj³,Siddiqi Mohammad I.³,Sinha Arun K.¹²

Affiliation:

1. Medicinal and Process Chemistry Division; CSIR-Central Drug Research Institute, Sector 10, Jankipuram Extension; Sitapur Road Lucknow 226031 India

2. Academy of Scientific and Innovative Research; Anusandhan Bhawan, 2 Rafi Marg New Delhi 110001 India

3. Molecular and Structural Biology Division; CSIR-Central Drug Research Institute, Sector 10, Jankipuram Extension; Sitapur Road Lucknow 226031 India

Funder

UGC

CSIR, New Delhi

SAIF-CDRI

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajoc.201700409/fullpdf

Reference92 articles.

1. In Situ Protection Methodology in Carbonyl Chemistry

2. Dialkylaluminum N,O-Dimethylhydroxylamine Complex as a Reagent to Mask Reactive Carbonyl Groups in Situ from Nucleophiles

3. Total synthesis of confertin via metal-promoted cyclization-lactonization

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