(Q40549126)

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Conformational Analysis, Thermal Rearrangement, and EI-MS Fragmentation Mechanism of (1(10)E,4E,6S,7R)-Germacradien-6-ol by (13)C-Labeling Experiments

scientific article published on 11 September 2015

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Europe PubMed Central

PubMed publication ID

21 September 2017

Conformational Analysis, Thermal Rearrangement, and EI-MS Fragmentation Mechanism of (1(10)E,4E,6S,7R)-Germacradien-6-ol by (13)C-Labeling Experiments (English)

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Europe PubMed Central

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21 September 2017

(+)-(1(10)E,4E,6S,7R)-germacradien-6-ol

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ChEBI release 2020-05-28

Jeroen S. Dickschat

8

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Jeroen S Dickschat

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Europe PubMed Central

PubMed publication ID

21 September 2017

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Patrick Rabe

1

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21 September 2017

Lena Barra

2

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21 September 2017

Jan Rinkel

3

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21 September 2017

Ramona Riclea

4

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21 September 2017

Christian A Citron

5

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21 September 2017

Tim A Klapschinski

6

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21 September 2017

Aron Janusko

7

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21 September 2017

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11 September 2015

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21 September 2017

Angewandte Chemie International Edition

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54

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21 September 2017

45

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21 September 2017

13448-13451

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21 September 2017

Terpenoids are widespread in actinomycetes: a correlation of secondary metabolism and genome data

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Volatiles from nineteen recently genome sequenced actinomycetes

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Identification and characterization of the linalool/nerolidol synthase from Streptomyces clavuligerus.

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Characterization of a novel sesquiterpene cyclase involved in (+)-caryolan-1-ol biosynthesis in Streptomyces griseus

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An improved technique for the rapid chemical characterisation of bacterial terpene cyclases.

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Terpene synthases are widely distributed in bacteria.

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Computational-guided discovery and characterization of a sesquiterpene synthase from Streptomyces clavuligerus

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Consequences of conformational preorganization in sesquiterpene biosynthesis: theoretical studies on the formation of the bisabolene, curcumene, acoradiene, zizaene, cedrene, duprezianene, and sesquithuriferol sesquiterpenes

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Pentalenene synthase. Analysis of active site residues by site-directed mutagenesis

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Terpenoid biosynthesis and the stereochemistry of enzyme-catalysed allylic addition—elimination reactions

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Effect of isotopically sensitive branching on product distribution for pentalenene synthase: support for a mechanism predicted by quantum chemistry

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Conformational Analysis of (+)-Germacrene A by Variable Temperature NMR and NOE Spectroscopy

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Identifiers

10.1002/ANIE.201507615

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

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