The first synthesis of a diynone from Echinacea pallida

George A. Kraus; Jaehoon Bae; Jessica Schuster

doi:10.1055/s-2005-918418

The first synthesis of a diynone from Echinacea pallida

George A. Kraus, Jaehoon Bae, Jessica Schuster

Research output: Contribution to journal › Article › peer-review

25 Scopus citations

Abstract

In order to provide an authentic standard and to generate pure material for biological testing, an efficient synthetic route to 1 was developed. This represents the first total synthesis of a major bioactive diynone from E. pallida.

Original language	English (US)
Article number	M01805SS
Pages (from-to)	3502-3504
Number of pages	3
Journal	Synthesis
Issue number	20
DOIs	https://doi.org/10.1055/s-2005-918418
State	Published - Dec 20 2005
Externally published	Yes

Keywords

Coupling reaction
Diynones
Selective alkyne reduction
Selective desilylation

Access

10.1055/s-2005-918418

OpenUrl availability

Full text

Cite this

@article{1ab7aa6a7add479bac4897f03dc6e841,

title = "The first synthesis of a diynone from Echinacea pallida",

abstract = "In order to provide an authentic standard and to generate pure material for biological testing, an efficient synthetic route to 1 was developed. This represents the first total synthesis of a major bioactive diynone from E. pallida.",

keywords = "Coupling reaction, Diynones, Selective alkyne reduction, Selective desilylation",

author = "Kraus, {George A.} and Jaehoon Bae and Jessica Schuster",

year = "2005",

month = dec,

day = "20",

doi = "10.1055/s-2005-918418",

language = "English (US)",

pages = "3502--3504",

journal = "Synthesis",

issn = "0039-7881",

publisher = "Georg Thieme Verlag",

number = "20",

}

TY - JOUR

T1 - The first synthesis of a diynone from Echinacea pallida

AU - Kraus, George A.

AU - Bae, Jaehoon

AU - Schuster, Jessica

PY - 2005/12/20

Y1 - 2005/12/20

N2 - In order to provide an authentic standard and to generate pure material for biological testing, an efficient synthetic route to 1 was developed. This represents the first total synthesis of a major bioactive diynone from E. pallida.

AB - In order to provide an authentic standard and to generate pure material for biological testing, an efficient synthetic route to 1 was developed. This represents the first total synthesis of a major bioactive diynone from E. pallida.

KW - Coupling reaction

KW - Diynones

KW - Selective alkyne reduction

KW - Selective desilylation

UR - http://www.scopus.com/inward/record.url?scp=29744468601&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=29744468601&partnerID=8YFLogxK

U2 - 10.1055/s-2005-918418

DO - 10.1055/s-2005-918418

M3 - Article

AN - SCOPUS:29744468601

SN - 0039-7881

SP - 3502

EP - 3504

JO - Synthesis

JF - Synthesis

IS - 20

M1 - M01805SS

ER -

The first synthesis of a diynone from Echinacea pallida

Abstract

Keywords

Access

OpenUrl availability

Other files and links

Fingerprint

Cite this