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Literature DB >> 21979838

Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.

Abstract

This review summarises the accumulated knowledge about the stereochemical courses of biosynthetic reactions to isoprenoids. Important pathways of the primary metabolism (mevalonate pathway, deoxyxylulose phosphate pathway) to the monomeric isoprenoid building blocks, the biosynthesis of the oligomeric linear precursors, and reactions to (poly-)cyclic mono-, sesqui-, and diterpenes are discussed.

Entities: Chemical

Mesh：

Substances：
Terpenes

Year: 2011 PMID： 21979838 DOI： 10.1039/c1np00063b

Source DB: PubMed Journal: Nat Prod Rep ISSN： 0265-0568 Impact factor: 13.423

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Cited

13 in total

1. Terpene cyclization catalysed inside a self-assembled cavity.

Authors: Q Zhang; K Tiefenbacher
Journal: Nat Chem Date: 2015-02-16 Impact factor: 24.427

Review 2. Traversing the fungal terpenome.

Authors: Maureen B Quin; Christopher M Flynn; Claudia Schmidt-Dannert
Journal: Nat Prod Rep Date: 2014-10 Impact factor: 13.423

3. Reducing Challenges in Organic Synthesis with Stereoselective Hydrogenation and Tandem Catalysis.

Authors: Patrick D Parker; Xintong Hou; Vy M Dong
Journal: J Am Chem Soc Date: 2021-04-23 Impact factor: 16.383

Review 4. Bacterial terpenome.

Authors: Jeffrey D Rudolf; Tyler A Alsup; Baofu Xu; Zining Li
Journal: Nat Prod Rep Date: 2021-05-26 Impact factor: 15.111

Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.

1. Terpene cyclization catalysed inside a self-assembled cavity.

Review 2. Traversing the fungal terpenome.

3. Reducing Challenges in Organic Synthesis with Stereoselective Hydrogenation and Tandem Catalysis.

Review 4. Bacterial terpenome.

5. A detailed view on 1,8-cineol biosynthesis by Streptomyces clavuligerus.

Review 6. Propolis Diterpenes as a Remarkable Bio-Source for Drug Discovery Development: A Review.

7. Purification and biochemical characterization of recombinant Persicaria minor β-sesquiphellandrene synthase.

Review 8. An Overview of Biotransformation and Toxicity of Diterpenes.

9. Revisiting the methionine salvage pathway and its paralogues.

10. Exploring natural biodiversity to expand access to microbial terpene synthesis.