(Q64996430)

English

Spirodionic acid, a novel metabolite from Streptomyces sp., part 2: total synthesis through a twofold michael addition as a selective spiroannelation strategy.

scientific article published in January 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

Spirodionic acid, a novel metabolite from Streptomyces sp., part 2: total synthesis through a twofold michael addition as a selective spiroannelation strategy. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

1 reference

Spirodionic acid

1 reference

Stephanie Grond

3

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

author name string

Jürgen Siewert

1

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

Adriana Textor

2

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

Paultheo von Zezschwitz

4

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

publication date

1 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

Chemistry—A European Journal

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

13

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

26

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

7424-7431

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

Synthesis of (-)-acorone and related spirocyclic sesquiterpenes

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CHEM.200601688

Lanthanide Triflates as Water-Tolerant Lewis Acids. Activation of Commercial Formaldehyde Solution and Use in the Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous Media

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CHEM.200601688

Structures of two remarkable dimerization products of sarkomycin

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CHEM.200601688

A general method of preparing functionalized spirocycles. Synthesis of spirovetivane sesquiterpenes

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CHEM.200601688

A phosphine-catalyzed [3+2] cycloaddition strategy leading to the first total synthesis of (-)-hinesol

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CHEM.200601688

Ozonolysis. II.1The Effect of Pyridine on the Ozonolysis of 4,22-Stigmastadien-3-one2

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/CHEM.200601688

Identifiers

10.1002/CHEM.200601688

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 July 2019

http://europepmc.org/abstract/MED/17583902

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