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)
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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).
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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2,2-Dimethoxypropane
CAS:77-76-9 |
C5H12O2 |
|
Delivery of therapeutic protein for prevention of neurodegen...
2015-01-01 [Exp. Neurol. 263 , 79-90, (2014)] |
|
Acetonation of L-pentoses and 6-deoxy-L-hexoses under kineti...
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 ...
1999-01-01 [Biotech. Histochem. 74(1) , 20-6, (1999)] |
|
Direct transesterification of lipids in mammalian tissue for...
1977-07-01 [J. Lipid Res. 18(4) , 540-3, (1977)] |
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