Formal Synthesis of (−)-Quinagolide: Diastereoselective Ring Expansion via a Bicyclic Aziridinium Ion Strategy to Access the Octahydrobenzo[g]quinoline Architecture-Reference-Cited by-同舟云学术

Formal Synthesis of (−)-Quinagolide: Diastereoselective Ring Expansion via a Bicyclic Aziridinium Ion Strategy to Access the Octahydrobenzo[g]quinoline Architecture

Published:2021-07-06 Issue:14 Volume:86 Page:9344-9352
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chavan Subhash P.¹²^ORCID,Kawale Sanket A.¹²,Pisal Mahesh M.¹²,Kadam Appasaheb L.¹²,Gonnade Rajesh G.²³^ORCID

Affiliation:

1. Division of Organic Chemistry, CSIR-National Chemical Laboratory, Pune 411008, India

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

3. Physical and Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India

Funder

Council of Scientific and Industrial Research, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c00603

Reference34 articles.

1. Dopamine Agonist Therapy for Hyperprolactinemia

2. Dopamine Agonist Therapy in Prolactinomas: When Can Treatment Be Discontinued?

3. Quinagolide – a valuable treatment option for hyperprolactinaemia

4. Prolactin (PRL) and Its Receptor: Actions, Signal Transduction Pathways and Phenotypes Observed in PRL Receptor Knockout Mice

5. Hyperprolactinemia

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