Total Synthesis of the Bacterial <i>ortho</i>-Quinol (+)-Strepantibin A through Iodyl-Type λ<sup>5</sup>-Iodane-Promoted Asymmetric Hydroxylative Phenol Dearomatization-Reference-Cited by-同舟云学术

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Total Synthesis of the Bacterial ortho-Quinol (+)-Strepantibin A through Iodyl-Type λ⁵-Iodane-Promoted Asymmetric Hydroxylative Phenol Dearomatization

Published:2024-07-11 Issue:29 Volume:26 Page:6086-6091
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wloch Morgan¹,Sun Zhaozhao¹,Valzer Emmanuel¹,Pouységu Laurent¹,Quideau Stéphane¹²^ORCID

Affiliation:

1. Université de Bordeaux, ISM (CNRS-UMR 5255), 351 cours de la Libération, 33405 Talence Cedex, France

2. Institut Universitaire de France, 1 rue Descartes, 75231 Paris Cedex 05, France

Funder

Minist?re de l'Enseignement sup?rieur, de la Recherche et de l'Innovation

Agence Nationale de la Recherche

Centre National de la Recherche Scientifique

China Scholarship Council

Institut Universitaire de France

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01653

Reference27 articles.

1. Strepantibins A–C: Hexokinase II Inhibitors from a Mud Dauber Wasp Associated Streptomyces sp.

2. ortho ‐Quinols in (Bio)Synthesis of Natural Products

3. Humulus lupulus- a story that begs to be told. A review

4. Total Synthesis of Wasabidienones B1 and B0 via SIBX-Mediated Hydroxylative Phenol Dearomatization

5. Bispericyclic Diels–Alder Dimerization of ortho ‐Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6‐Step Synthesis of (+)‐Maytenone

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