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  Bypassing stereoselectivity in the early steps of alkaloid biosynthesis

Bernhardt, P., Yerkes, N., & O'Connor, S. E. (2009). Bypassing stereoselectivity in the early steps of alkaloid biosynthesis. Organic & Biomolecular Chemistry, 7(20), 4166-4168. doi:10.1039/b916027m.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0002-A98C-2 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-3D93-D
Genre: Journal Article

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SOC017.pdf (Publisher version), 160KB
 
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https://www.ncbi.nlm.nih.gov/pubmed/19795053 (Postprint)
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 Creators:
Bernhardt, Peter1, Author
Yerkes, Nancy1, Author
O'Connor, Sarah E.1, Author           
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1external, ou_persistent22              

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Free keywords: STRICTOSIDINE GLUCOSIDASE; CATHARANTHUS-ROSEUS; RAUBASINE; SYNTHASE; ENZYME; TETRAHYDROALSTONINE; KEYChemistry;
 Abstract: Total synthesis of glycosylated seco-iridoid stereoisomers allows the identification and bypassing of the stereoselectivity of early steps in monoterpene indole alkaloid biosynthesis.

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Language(s): eng - English
 Dates: 2009
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: Other: SOC017
DOI: 10.1039/b916027m
 Degree: -

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Title: Organic & Biomolecular Chemistry
  Other : Organic and Biomolecular Chemistry
  Abbreviation : Org. Biomol. Chem.
Source Genre: Journal
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Publ. Info: Cambridge : Royal Society of Chemistry
Pages: - Volume / Issue: 7 (20) Sequence Number: - Start / End Page: 4166 - 4168 Identifier: ISSN: 1477-0520
CoNE: https://pure.mpg.de/cone/journals/resource/954925269322