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  2. Ribosomally synthesized and post-translationally modified ...

    en.wikipedia.org/wiki/Ribosomally_synthesized...

    Ribosomally synthesized and post-translationally modified peptides (RiPPs), also known as ribosomal natural products, are a diverse class of natural products of ribosomal origin. [1] Consisting of more than 20 sub-classes, RiPPs are produced by a variety of organisms , including prokaryotes , eukaryotes , and archaea , and they possess a wide ...

  3. Natural product - Wikipedia

    en.wikipedia.org/wiki/Natural_product

    In addition, natural products are prepared by organic synthesis, to provide confirmation of their structure, or to give access to larger quantities of natural products of interest. In this process, the structure of some natural products have been revised, [140] [141] [142] and the challenge of synthesising natural products has led to the ...

  4. Biomimetic synthesis - Wikipedia

    en.wikipedia.org/wiki/Biomimetic_synthesis

    Biomimetic synthesis is an area of organic chemical synthesis that is specifically biologically inspired. The term encompasses both the testing of a "biogenetic hypothesis" (conjectured course of a biosynthesis in nature) through execution of a series of reactions designed to parallel the proposed biosynthesis, as well as programs of study where a synthetic reaction or reactions aimed at a ...

  5. Dynamic kinetic resolution in asymmetric synthesis - Wikipedia

    en.wikipedia.org/wiki/Dynamic_Kinetic_Resolution...

    Dynamic kinetic resolution has also been applied to the total synthesis of a variety of natural products. After Bäckvall's discoveries in 2007, he employed another enzyme-metal coupled reaction to synthesize the natural product (R)-Bufuralol. [18] Condensed reaction scheme for (R)-Bufuralol showing the key DKR step in the synthetic pathway.

  6. Ullmann reaction - Wikipedia

    en.wikipedia.org/wiki/Ullmann_reaction

    Aryl-Aryl bond formation is a fundamental tool in modern organic synthesis, with applications spanning natural product synthesis, pharmaceuticals, agrochemicals, and the development of commercial dyes and polyaromatics. With over a century of history, the Ullmann reaction has been one of the first to use a transition metal, primarily copper, in ...

  7. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    Its applications include pharmaceuticals, natural products, organic materials, and nanomaterials. [1] Specific examples include its use in the synthesis of tazarotene , [ 2 ] which is a treatment for psoriasis and acne , and in the preparation of SIB-1508Y, also known as Altinicline , [ 3 ] a nicotinic receptor agonist .

  8. Simmons–Smith reaction - Wikipedia

    en.wikipedia.org/wiki/Simmons–Smith_reaction

    The β-lactamase inhibitor Cilastatin provides an instructive example of Simmons-Smith reactivity in natural products synthesis. An allyl substituent on the starting material is Simmons-Smith cyclopropanated, and the carboxylic acid is subsequently deprotected via ozonolysis to form the precursor .

  9. Negishi coupling - Wikipedia

    en.wikipedia.org/wiki/Negishi_coupling

    The Negishi coupling was implemented in the synthesis of δ-trans-tocotrienoloic acid by Hecht and Maloney coupling the sp 3 homopropargyl zinc reagent 8 with sp 2 vinyl iodide 9. [43] The reaction proceeded with quantitative yield, coupling fragments mid-synthesis en route to the stereoselectively synthesized natural product δ-trans ...

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