A Tandem Semipinacol Rearrangement/Aldehyde Arylation or Alkylation of Trisubstituted 2,3-Epoxy Alcohols with Grignard Reagents for Functionalized 1,3-Diols-Reference-Cited by-同舟云学术

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A Tandem Semipinacol Rearrangement/Aldehyde Arylation or Alkylation of Trisubstituted 2,3-Epoxy Alcohols with Grignard Reagents for Functionalized 1,3-Diols

Published:2022-06-09 Issue:12 Volume:87 Page:7696-7711
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kumar Amit¹,Sharma Gaurav²³,Shukla Sanjeev K.²³,Panda Gautam¹³^ORCID

Affiliation:

1. Medicinal & Process Chemistry Division, CSIR-Central Drug Research Institute, Sector 10, Jankipuram extension, Sitapur Road, Lucknow 226031, UP, India

2. Sophisticated Analytical Instrument Facility & Research, CSIR-Central Drug Research Institute, Sector 10, Jankipuram extension, Sitapur Road, Lucknow 226031, UP, India

3. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India

Funder

Council of Scientific and Industrial Research

Research Grants Council, University Grants Committee

Department of Biotechnology , Ministry of Science and Technology

Department of Science and Technology, Ministry of Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00267

Reference49 articles.

1. Enantioselective synthesis of .beta.-hydroxy .delta.-lactones: a new approach to the synthetic congeners of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors

2. Diastereoselective synthesis of syn-3,5-dihydroxyesters via ruthenium-catalyzed asymmetric transfer hydrogenation

3. Homogeneous asymmetric hydrogenation of functionalized ketones

4. Ruthenium-catalyzed asymmetric reduction of 1,3-diketones using transfer hydrogenation

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