Synthesis and biological activity of 28-homobrassinolide and analogues
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[1] T. Mcmorris,et al. Improved synthesis of 24-epibrassinolide from ergosterol , 1993 .
[2] R. Peracaula,et al. Use of dihydroquinidine 9-O-(9'-phenanthryl) ether in osmium-catalyzed asymmetric dihydroxylation in the synthesis of brassinosteroids , 1992 .
[3] M. Baker,et al. Effect of brassinolide on gene expression in elongating soybean epicotyls. , 1992, Plant physiology.
[4] Jens Hartung,et al. The Osmium-Catalyzed Asymmetric Dihydroxylation: A New Ligand Class and a Process Improvement , 1992 .
[5] P. Ciuffreda,et al. A convenient isomerization of 6-oxo-3α,5-cyclo-5α-steroids to 6-oxo-Δ2-5α-steroids , 1985, Steroids.
[6] T. Mcmorris,et al. A novel synthesis of brassinolide , 1984 .
[7] W. Lusby,et al. Synthesis of brassinosteroids and relationship of structure to plant growth-promoting effects , 1982, Steroids.
[8] J. Yopp,et al. Brassinolide, a growth-promoting steroidal lactone. I. Activity in selected auxin bioassays , 1981 .
[9] E. Mosettig,et al. The Solvolysis of Stigmasteryl Tosylate , 1963 .
[10] S. Takatsuto,et al. Structure-activity relationship of brassinosteroids , 1983 .
[11] K. Mori,et al. Synthesis of (22S, 23S)-homobrassinolide and brassinolide from stigmasterol , 1982 .