Steroids 2010-01-01

Preparation and synthetic application of partially protected brassinosteroids.

Vladimir A Khripach, Vladimir N Zhabinskii, Yuliya Y Zhiburtovich, Galina V Ivanova, Olga V Konstantinova, Dmitrii V Tsavlovskii, Sybille Lorenz, Bernd Schneider

Index: Steroids 75(1) , 27-33, (2010)

Full Text: HTML

Abstract

Preparation of partially protected brassinosteroids is achieved through the reaction of the source material (24-epicastasterone and 24-epibrassinolide) with diol-specific reagents (2,2-dimethoxypropane and methylboronic acid). The obtained products were shown to be useful synthetic intermediates for further preparation of minor representatives of this class of natural phytohormones (such as 3,24-diepicastasterone and 3-dehydro-24-epibrassinolide).


Related Compounds

Related Articles:

Delivery of therapeutic protein for prevention of neurodegenerative changes: comparison of different CSF-delivery methods.

2015-01-01

[Exp. Neurol. 263 , 79-90, (2014)]

Acetonation of L-pentoses and 6-deoxy-L-hexoses under kinetic control using heterogeneous acid catalysts.

2010-07-19

[Carbohydr. Res. 345(11) , 1548-54, (2010)]

Chemical dehydration for rapid paraffin embedding.

1994-09-01

[Biotech. Histochem. 69(5) , 289-90, (1994)]

Chemical dehydration of specimens with 2,2-dimethoxypropane (DMP) for paraffin processing of animal tissues: practical and economic advantages over dehydration in ethanol.

1999-01-01

[Biotech. Histochem. 74(1) , 20-6, (1999)]

Direct transesterification of lipids in mammalian tissue for fatty acid analysis via dehydration with 2,2'-dimethoxypropane.

1977-07-01

[J. Lipid Res. 18(4) , 540-3, (1977)]

More Articles...