Biological formation of pyrroles: Nature's logic and enzymatic machinery-Reference-Cited by-同舟云学术

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Biological formation of pyrroles: Nature's logic and enzymatic machinery

Published:2006 Issue:4 Volume:23 Page:517
ISSN:0265-0568
Container-title:Natural Product Reports
language:en
Short-container-title:Nat. Prod. Rep.

Author:

Walsh Christopher T.,Garneau-Tsodikova Sylvie,Howard-Jones Annaleise R.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2006/NP/B605245M

Reference96 articles.

1. Proof by synthesis that unrearranged hydroxymethylbilane is the product from deaminase and the substrate for cosynthetase in the biosynthesis of uro'gen-III

2. Microbial biosynthesis of halometabolites

3. Biosynthesis of pyrrolnitrin and other phenylpyrrole derivatives by bacteria (up to mid-1999)

4. Conversion of L-Proline to Pyrrolyl-2-Carboxyl-S-PCP during Undecylprodigiosin and Pyoluteorin Biosynthesis

5. Analysis of the prodiginine biosynthesis gene cluster of Streptomyces coelicolor A3(2): new mechanisms for chain initiation and termination in modular multienzymes

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2. Allostreptopyrroles A–E, β-alkylpyrrole derivatives from an actinomycete Allostreptomyces sp. RD068384;Beilstein Journal of Organic Chemistry;2024-08-13

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4. Depolymerization of tubulin as the main molecular mechanism of the cytotoxic and antitumor activity of pyrrole-containing heterocyclic compounds;Advances in Molecular Oncology;2024-06-28

5. Modular Access to Tetrasubstituted N−H Pyrroles by Catalytic 1,3‐Dipolar Cycloaddition of Azomethine Ylides and α,β‐Ynones;European Journal of Organic Chemistry;2024-06-10

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