(Q46536414)

English

Conformational energetics of cationic backbone rearrangements in triterpenoid biosynthesis provide an insight into enzymatic control of product

scientific article published on 18 June 2008

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

Conformational energetics of cationic backbone rearrangements in triterpenoid biosynthesis provide an insight into enzymatic control of product (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

Elias James Corey

3

object named as

E J Corey

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

author name string

László Kürti

1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

Rong-Jie Chein

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

language of work or name

0 references

publication date

18 June 2008

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

130

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

28

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

9031-9036

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

A case study in biomimetic total synthesis: polyolefin carbocyclizations to terpenes and steroids

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Enzyme Mechanisms for Polycyclic Triterpene Formation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Mechanistic insights into triterpene synthesis from quantum mechanical calculations. Detection of systematic errors in B3LYP cyclization energies

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

On the origins of triterpenoid skeletal diversity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Balancing Kinetic and Thermodynamic Control: the Mechanism of Carbocation Cyclization by Squalene Cyclase

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Q-Chem 2.0: a high-performanceab initio electronic structure program package

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Concerted nature of AB ring formation in the enzymatic cyclization of squalene to hopenes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Studies on the Substrate Binding Segments and Catalytic Action of Lanosterol Synthase. Affinity Labeling with Carbocations Derived from Mechanism-Based Analogs of 2,3-Oxidosqualene and Site-Directed Mutagenesis Probes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Concomitant C-ring Expansion and D-ring formation in lanosterol biosynthesis from squalene without violation of Markovnikov's rule

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

An oxidosqualene cyclase makes numerous products by diverse mechanisms: a challenge to prevailing concepts of triterpene biosynthesis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Formation of the C ring in the lanosterol biosynthesis from squalene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Methodology for the Preparation of Pure RecombinantS. cerevisiaeLanosterol Synthase Using a Baculovirus Expression System. Evidence That Oxirane Cleavage and A-Ring Formation Are Concerted in the Biosynthesis of Lanosterol from 2,3-Oxidosqualene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA800980H

Identifiers

10.1021/JA800980H

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18558677

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q46536414&oldid=2116915870"