phytoestrogens and 5-6-11-12-17-18-hexahydrocyclononatriindole

phytoestrogens has been researched along with 5-6-11-12-17-18-hexahydrocyclononatriindole* in 1 studies

Other Studies

1 other study(ies) available for phytoestrogens and 5-6-11-12-17-18-hexahydrocyclononatriindole

Article	Year
Convenient synthesis of 5,6,11,12,17,18- hexahydrocyclononal[1,2-b:4,5-b':7,8-b'']triindole, a novel phytoestrogen. The Journal of organic chemistry, 2003, Jan-10, Volume: 68, Issue:1 An efficient one-pot synthesis is described of 5,6,11,12,17,18-hexahydrocyclononal[1,2-b:4,5-b':7,8-b'']triindole (CTr), a potent estrogen agonist from food plants. For the procedure, gramine is treated with dimethyl sulfate and sodium in ethanol at room temperature. Quenching of the reaction with water and workup of the product provides CTr in approximately 75% yield. Topics: Brassica; Catalysis; Estrogens, Non-Steroidal; Indoles; Isoflavones; Magnetic Resonance Spectroscopy; Molecular Structure; Phytoestrogens; Plant Preparations; Receptors, Estrogen; Structure-Activity Relationship; Temperature; Water	2003

Article

Year

Convenient synthesis of 5,6,11,12,17,18- hexahydrocyclononal[1,2-b:4,5-b':7,8-b'']triindole, a novel phytoestrogen.

The Journal of organic chemistry, 2003, Jan-10, Volume: 68, Issue:1

An efficient one-pot synthesis is described of 5,6,11,12,17,18-hexahydrocyclononal[1,2-b:4,5-b':7,8-b'']triindole (CTr), a potent estrogen agonist from food plants. For the procedure, gramine is treated with dimethyl sulfate and sodium in ethanol at room temperature. Quenching of the reaction with water and workup of the product provides CTr in approximately 75% yield.

Topics: Brassica; Catalysis; Estrogens, Non-Steroidal; Indoles; Isoflavones; Magnetic Resonance Spectroscopy; Molecular Structure; Phytoestrogens; Plant Preparations; Receptors, Estrogen; Structure-Activity Relationship; Temperature; Water

2003