Proton-Sensitive Free-Radical Dimer Evolution Is a Critical Control Point for the Synthesis of Δ2,2′-Bibenzothiazines-Reference-Cited by-同舟云学术

Proton-Sensitive Free-Radical Dimer Evolution Is a Critical Control Point for the Synthesis of Δ2,2′-Bibenzothiazines

Published:2020-08-26 Issue:17 Volume:85 Page:11440-11448
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Valgimigli Luca¹^ORCID,Alfieri Maria Laura²,Amorati Riccardo¹^ORCID,Baschieri Andrea¹,Crescenzi Orlando²^ORCID,Napolitano Alessandra²^ORCID,d’Ischia Marco²^ORCID

Affiliation:

1. Department of Chemistry “Giacomo Ciamician”, University of Bologna, Bologna I-40126, Italy

2. Department of Chemical Sciences, University of Naples Federico II, Naples I-80126, Italy

Funder

Kao Corporation

Universit? di Bologna

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01520

Reference37 articles.

1. Zinc-Catalyzed Oxidation of 5-S-Cysteinyldopa to 2,2‘-Bi(2H-1,4-benzothiazine): Tracking the Biosynthetic Pathway of Trichochromes, the Characteristic Pigments of Red Hair

2. Oxidative Polymerization of the Pheomelanin Precursor 5-Hydroxy-1,4-benzothiazinylalanine: A New Hint to the Pigment Structure

3. A New Insight in the Biosynthesis of Pheomelanins: Characterization of a Labile 1,4-Benzothiazine Intermediate

4. Red Hair Benzothiazines and Benzothiazoles: Mutation-Inspired Chemistry in the Quest for Functionality

5. Trichocyanines: a Red-Hair-Inspired Modular Platform for Dye-Based One-Time-Pad Molecular Cryptography

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