Intramolecular thiomaleimide [2 + 2] photocycloadditions: stereoselective control for disulfide stapling and observation of excited state intermediates by transient absorption spectroscopy
Author:
Affiliation:
1. Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK
2. Department of Chemistry, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK
Abstract
Funder
Engineering and Physical Sciences Research Council
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/SC/D1SC06804K
Reference46 articles.
1. Chemical Modification of Proteins at Cysteine: Opportunities in Chemistry and Biology
2. Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation
3. Cysteine-Based Coupling: Challenges and Solutions
4. An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy
5. Antibody–drug conjugates: targeted drug delivery for cancer
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1. Chemical technology principles for selective bioconjugation of proteins and antibodies;Chemical Society Reviews;2024
2. A Light‐Induced Decarboxylative‐Elimination of Substituted Maleimides as a Strategy Towards Triggered Photorelease;European Journal of Organic Chemistry;2023-04-27
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