Total Synthesis of (−)‐Salinosporamide A via a Late Stage C−H Insertion-Reference-Cited by-同舟云学术

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Total Synthesis of (−)‐Salinosporamide A via a Late Stage C−H Insertion

Published:2019-07-22 Issue:30 Volume:58 Page:10110-10113
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Gholami Hadi¹^ORCID,Kulshrestha Aman¹,Favor Olivia K.¹,Staples Richard J.¹,Borhan Babak¹^ORCID

Affiliation:

1. Department of ChemistryMichigan State University E. Lansing MI 48824 USA

Funder

National Institute of General Medical Sciences

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201900340

Reference58 articles.

1. Salinosporamide A: A Highly Cytotoxic Proteasome Inhibitor from a Novel Microbial Source, a Marine Bacterium of the New Genus Salinospora

2.

3. Salinosporamide Natural Products: Potent 20 S Proteasome Inhibitors as Promising Cancer Chemotherapeutics

4. Salinosporamid-Naturstoffe: potente Inhibitoren des 20S-Proteasoms als vielversprechende Krebs-Chemotherapeutika

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1. Organocatalytic Stereoselective Decarboxylative Addition of α‐Amido Malonic Acid Half Oxyesters to Isatins;Advanced Synthesis & Catalysis;2024-01-16

2. First Asymmetric Total Synthesis of Salinosporamides D and I Using Memory of Chirality and Dynamic Kinetic Resolution;European Journal of Organic Chemistry;2023-09-18

3. Evolution of a Strategy for Concise Enantioselective Total Synthesis of the Salinosporamide Family of Natural Products;Angewandte Chemie International Edition;2022-09-02

4. Evolution of a Strategy for Concise Enantioselective Total Synthesis of the Salinosporamide Family of Natural Products;Angewandte Chemie;2022-09-02

5. Radical Allylation, Vinylation, Allenylation, Alkynylation, and Propargylation Reactions Using Tin Reagents;Organic Reactions;2022-06-13

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