138052-02-5

Upstream product

• 111917-81-8 (1R^*,3S^*,7S^*,8S^*)-7-(tert-Butyldimethylsilyloxy)-2,4-dioxatricyclo<6.2.1.0^3,7>undecan-5-ol 
• 108-98-5 thiophenol 
• 111917-75-0 (1R^*,4R^*,5S^*)-4-Hydroxy-2-oxabicyclo<3.2.1>octan-3-one 
• 111917-76-1 (1R^*,4R^*,5S^*)-4-(tert-Butyldimethylsilyloxy)-2-oxabicyclo<3.2.1>octan-3-one 
• 111917-73-8 (1R^*,3S^*,7R^*,8S^*)-7-Hydroxy-2,4-dioxatricyclo<6.2.1.0^3,7>undec-5-ene 
• 111917-77-2 (1R^*,4S^*,5S^*)-4-(tert-Butyldimethylsilyloxy)-4-(prop-2-enyl)-2-oxabicyclo<3.2.1>octan-3-one 
• 111917-74-9 (1R^*,4S^*,5S^*)-4-(tert-Butyldimethylsilyloxy)-4-(prop-2-enyl)-2-oxabicyclo<3.2.1>octan-3-ol 
• 5724-61-8 2-oxabicyclo[3.2.1]octan-3-one 

Downstream Products

• 111917-83-0 (1R^*,3R^*,7S^*,8S^*)-7-(tert-Butyldimethylsilyloxy)-5-phenylsulphoxide-2,4-dioxatricyclo<6.2.1.0^3,7>undecane 

Relevant academic research and scientific papers

SYNTHESIS OF A HYDROXY DIHYDROFURAN ACETAL RELATED TO AZADIRACHTIN: A POTENT INSECT ANTIFEEDANT

The synthesis of novel hydroxy dihydro and tetrahydrofuran acetals modelled on the insect antifeedant azadirachtin is described.

Chemistry of insect antifeedants from Azadirachta indica (Part 8):1 Synthesis of hydroxydihydrofuran acetal fragments for biological evaluation and azadirachtin total synthesis studies

The work describes a unified strategy towards the preparation of model hydroxydihydrofuran acetal fragments (2) (3) and (45) common to the potent insect antifeedant and growth disruption agent azadirachtin (1). These units, along with other analogues, wer