Highly Stereoselective Diels–Alder-Based Strategy for the Synthesis of 3-<i>epi</i>-Formicin A and 1-<i>epi</i>-Formicin B-Reference-Cited by-同舟云学术

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Highly Stereoselective Diels–Alder-Based Strategy for the Synthesis of 3-epi-Formicin A and 1-epi-Formicin B

Published:2024-04-29 Issue:18 Volume:26 Page:3961-3965
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Khamkar Sunil L.¹²,Handore Kishor L.¹³^ORCID,Shinde Harish M.²,Reddy D. Srinivasa¹⁴^ORCID

Affiliation:

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

2. BASF Innovation Campus Mumbai, BASF Chemicals India Pvt. Ltd., Plot No. 12, TTC Area Thane Belapur Road, Turbhe, Navi Mumbai 400705, India

3. Organic Chemistry Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, India

4. Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India

Funder

Science and Engineering Research Board

BASF Chemicals India Pvt. Ltd.

BASF Innovation Campus Mumbai

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01209

Reference44 articles.

1. Formicins, N-Acetylcysteamine-Bearing Indenone Thioesters from a Wood Ant-Associated Bacterium

2. The LKB1 tumor suppressor negatively regulates mTOR signaling

3. Targeting LKB1 in cancer – exposing and exploiting vulnerabilities

4. Loss of the tumor suppressor LKB1 promotes metabolic reprogramming of cancer cells via HIF-1

5. Structural analysis of the dual-function thioesterase SAV606 unravels the mechanism of Michael addition of glycine to an α,β-unsaturated thioester

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