7α-Alkoxyestra-1,3,5(10)-trienes

Takumi Yasuda; Yuji Shima; Keiko Ideta; Cristina Das Neves Oliveira; Thies Thiemann

doi:10.3184/030823408X287140

7α-Alkoxyestra-1,3,5(10)-trienes

Takumi Yasuda
, Yuji Shima
, Keiko Ideta
, Cristina Das Neves Oliveira
, Thies Thiemann

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

2 Citations (Scopus)

Abstract

α-Alkoxyestradiols were prepared through LiAlH₄ reduction of a suitably protected 6α,7α-epoxyestra-1,3,5(10)-trien-3-ol-17- one, alkylation of the resultant 7α-hydroxyestra-1,3,5(10)-trien-3-ol-17- one derivative and subsequent transformation of the C17 functionality.

Original language	English
Pages (from-to)	32-37
Number of pages	6
Journal	Journal of Chemical Research
Issue number	1
DOIs	https://doi.org/10.3184/030823408X287140
Publication status	Published - Jan 2008
Externally published	Yes

Keywords

Estradiol
Ethers
Steroids

ASJC Scopus subject areas

General Chemistry

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10.3184/030823408X287140

Cite this

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title = "7α-Alkoxyestra-1,3,5(10)-trienes",

abstract = "α-Alkoxyestradiols were prepared through LiAlH4 reduction of a suitably protected 6α,7α-epoxyestra-1,3,5(10)-trien-3-ol-17- one, alkylation of the resultant 7α-hydroxyestra-1,3,5(10)-trien-3-ol-17- one derivative and subsequent transformation of the C17 functionality.",

keywords = "Estradiol, Ethers, Steroids",

author = "Takumi Yasuda and Yuji Shima and Keiko Ideta and \{Das Neves Oliveira\}, Cristina and Thies Thiemann",

year = "2008",

month = jan,

doi = "10.3184/030823408X287140",

language = "English",

pages = "32--37",

journal = "Journal of Chemical Research",

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publisher = "Scientific Reviews 2000 Ltd.",

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T1 - 7α-Alkoxyestra-1,3,5(10)-trienes

AU - Yasuda, Takumi

AU - Shima, Yuji

AU - Ideta, Keiko

AU - Das Neves Oliveira, Cristina

AU - Thiemann, Thies

PY - 2008/1

Y1 - 2008/1

N2 - α-Alkoxyestradiols were prepared through LiAlH4 reduction of a suitably protected 6α,7α-epoxyestra-1,3,5(10)-trien-3-ol-17- one, alkylation of the resultant 7α-hydroxyestra-1,3,5(10)-trien-3-ol-17- one derivative and subsequent transformation of the C17 functionality.

AB - α-Alkoxyestradiols were prepared through LiAlH4 reduction of a suitably protected 6α,7α-epoxyestra-1,3,5(10)-trien-3-ol-17- one, alkylation of the resultant 7α-hydroxyestra-1,3,5(10)-trien-3-ol-17- one derivative and subsequent transformation of the C17 functionality.

KW - Estradiol

KW - Ethers

KW - Steroids

UR - https://www.scopus.com/pages/publications/42349097797

UR - https://www.scopus.com/pages/publications/42349097797#tab=citedBy

U2 - 10.3184/030823408X287140

DO - 10.3184/030823408X287140

M3 - Article

AN - SCOPUS:42349097797

SN - 0308-2342

SP - 32

EP - 37

JO - Journal of Chemical Research

JF - Journal of Chemical Research

IS - 1

ER -

7α-Alkoxyestra-1,3,5(10)-trienes

Abstract

Keywords

ASJC Scopus subject areas

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