2007
DOI: 10.1016/j.tet.2006.11.063
|View full text |Cite
|
Sign up to set email alerts
|

Stereoselective synthesis and moulting activity of integristerone A and analogues

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2007
2007
2012
2012

Publication Types

Select...
4
2

Relationship

0
6

Authors

Journals

citations
Cited by 7 publications
(2 citation statements)
references
References 10 publications
0
2
0
Order By: Relevance
“…Initially, a 20-hydroxyecdysone derivative bearing a 1,2-unsaturation was prepared [25]. Tritiation of this compound was performed by Moravek Biochemicals Inc. (Brea, CA92821, USA) using 10% Pd/C as catalyst with tritium gas (EtOH solution, 1 h, ratio of compound/catalyst 3:1) and yielded 50 mCi [1␣,2␣-3 H]2-deoxy-20-hydroxyecdysone (spec.…”
Section: Preparation Of [1˛2˛-3 H 2 ]20ementioning
confidence: 99%
“…Initially, a 20-hydroxyecdysone derivative bearing a 1,2-unsaturation was prepared [25]. Tritiation of this compound was performed by Moravek Biochemicals Inc. (Brea, CA92821, USA) using 10% Pd/C as catalyst with tritium gas (EtOH solution, 1 h, ratio of compound/catalyst 3:1) and yielded 50 mCi [1␣,2␣-3 H]2-deoxy-20-hydroxyecdysone (spec.…”
Section: Preparation Of [1˛2˛-3 H 2 ]20ementioning
confidence: 99%
“…[242][243][244][245] The synthesis and moulting hormone activity of integristerone A (1b,20-dihydroxyecdysone) 55 has been reported. 246 A number of ponasterone A derivatives have been prepared and their binding to the ecdysone receptor has been evaluated. 247 Over sixty brassinosteroids are known.…”
Section: Cholestanesmentioning
confidence: 99%