Stereochemical investigations of the Tetrahymena cyclase, a model system for euphane/tirucallane biosynthesis-Reference-Cited by-同舟云学术

Stereochemical investigations of the Tetrahymena cyclase, a model system for euphane/tirucallane biosynthesis

Published:2017 Issue:13 Volume:15 Page:2823-2830
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Giner José-Luis¹²³⁴⁵^ORCID,Feng Ju¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. State University of New York

3. College of Environmental Science and Forestry

4. Syracuse

5. USA

Abstract

The squalene cyclase of Tetrahymena pyriformis cyclizes 2,3-dihydrosqualene to euph-7-ene; after truncation of the substrate, “tirucall-7-enes” are formed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00296C

Reference18 articles.

1. Zur Kenntnis der Triterpene. 182. Mitteilung. Konstitution und Konfiguration von Euphol und iso-Euphenol

2. Zur Kenntnis der Triterpene. 183. Mitteilung. Über die Konstitution und Konfiguration von Tirucallol, Euphorbol und Elemadienolsäure

3. Zur Kenntnis der Triterpene. 190. Mitteilung. Eine stereochemische Interpretation der biogenetischen Isoprenregel bei den Triterpenen

4. Revisited after 50 Years: The ‘Stereochemical Interpretation of the Biogenetic Isoprene Rule for the Triterpenes’

5. Enyzmatic cyclization of 2,3-dihydrosqualene into euph-7-ene by a cell-free system from the protozoon Tetrahymena pyriformis

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