17a-Oxa-17a-homobrassinosteroid Analogues

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Title:17a-Oxa-17a-homobrassinosteroid Analogues
Creators:
Kohout, Ladislav
Slavíková, Barbora
Strnad, Miroslav
Journal or Publication Title:
Collection of Czechoslovak Chemical Communications, 63, 5, pp. 646-654
Uncontrolled Keywords:Brassinolide activity, Brassinolide analogues, Steroids, Brassinosteroid dilactones, Second bean internode bioassay

Abstract

Synthesis of a 17a-oxa-17a-homobrassinosteroids, <i>i.e.</i> brassinosteroids having two lactone rings, is described. In the bean second internode bioassay, dilactone <strong>16</strong> was the most effective of the compounds synthesized. In the same test, the castasterone analogue <strong>12</strong> exhibited a growth-retarding effect.

Title:17a-Oxa-17a-homobrassinosteroid Analogues
Creators:
Kohout, Ladislav
Slavíková, Barbora
Strnad, Miroslav
Uncontrolled Keywords:Brassinolide activity, Brassinolide analogues, Steroids, Brassinosteroid dilactones, Second bean internode bioassay
Divisions:Life and Chemical Sciences > Institute of Organic Chemistry and Biochemistry > Collection of Czechoslovak Chemical Communications
Journal or Publication Title:Collection of Czechoslovak Chemical Communications
Volume:63
Number:5
Page Range:pp. 646-654
ISSN:0010-0765
E-ISSN:1212-6950
Publisher:Institute of Organic Chemistry and Biochemistry
Related URLs:
URLURL Type
http://dx.doi.org/10.1135/cccc19980646UNSPECIFIED
ID Code:1330
Item Type:Article
Deposited On:06 Feb 2009 17:08
Last Modified:06 Feb 2009 16:08

Citation

Kohout, Ladislav; Slavíková, Barbora; Strnad, Miroslav (1998) 17a-Oxa-17a-homobrassinosteroid Analogues. Collection of Czechoslovak Chemical Communications, 63 (5). pp. 646-654. ISSN 0010-0765

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