A series of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes

Thies Thiemann; Kuniharu Umeno; Eiko Inohae; Masao Imai; Yuji Shima; Shuntaro Mataka

doi:10.3184/030823402103170312

A series of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes

Thies Thiemann, Kuniharu Umeno, Eiko Inohae, Masao Imai, Yuji Shima, Shuntaro Mataka

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

10 Citations (Scopus)

Abstract

A number of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes as potential ligands for the estrogen receptor ERα have been prepared using either a conjugate addition of α,ω-iodoalkanenitriles or a Michael addition to steroidal ketone 3 as the key step.

Original language	English
Pages (from-to)	1-3
Number of pages	3
Journal	Journal of Chemical Research - Part S
Issue number	1
DOIs	https://doi.org/10.3184/030823402103170312
Publication status	Published - 2002
Externally published	Yes

Keywords

Conjugate addition
Estrogens
Estrone
Phase transfer catalysis
Phosphorane
Shapiro reaction
Steroids
Wittig-olefination

ASJC Scopus subject areas

General Chemistry

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10.3184/030823402103170312

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abstract = "A number of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes as potential ligands for the estrogen receptor ERα have been prepared using either a conjugate addition of α,ω-iodoalkanenitriles or a Michael addition to steroidal ketone 3 as the key step.",

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T1 - A series of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes

AU - Thiemann, Thies

AU - Umeno, Kuniharu

AU - Inohae, Eiko

AU - Imai, Masao

AU - Shima, Yuji

AU - Mataka, Shuntaro

PY - 2002

Y1 - 2002

N2 - A number of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes as potential ligands for the estrogen receptor ERα have been prepared using either a conjugate addition of α,ω-iodoalkanenitriles or a Michael addition to steroidal ketone 3 as the key step.

AB - A number of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes as potential ligands for the estrogen receptor ERα have been prepared using either a conjugate addition of α,ω-iodoalkanenitriles or a Michael addition to steroidal ketone 3 as the key step.

KW - Conjugate addition

KW - Estrogens

KW - Estrone

KW - Phase transfer catalysis

KW - Phosphorane

KW - Shapiro reaction

KW - Steroids

KW - Wittig-olefination

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A series of 7-ω-carboxamidoalkyl-substituted estra-1,3,5(10),6-tetraenes

Abstract

Keywords

ASJC Scopus subject areas

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