211738-25-9Relevant academic research and scientific papers
Exploring an alternative approach to the synthesis of arylalkyl and indolylmethyl glucosinolates
Cassel, Stephanie,Casenave, Brigitte,Deleris, Gerard,Latxague, Laurent,Rollin, Patrick
, p. 8515 - 8524 (1998)
A new approach to the elaboration of hydroximoyl chlorides - key- compounds in the synthesis of glucosinolates - based on nitrovinyl intermediates was explored in the case of arylalkyl conjugates and their indolylmethyl counterparts.
Rhodium-catalyzed asymmetric addition of arylboronic acids to indolylnitroalkenes
Xing, Junwei,Chen, Guihua,Cao, Peng,Liao, Jian
supporting information; experimental part, p. 1230 - 1236 (2012/04/10)
Indolylnitroethanes and their derivatives are key intermediates to many bioactive structures. Most approaches to access chiral indolylnitroethanes involve organocatalyzed or metal-catalyzed asymmetric Friedel-Crafts reaction of indoles with nitroalkenes.
Efficient one-pot synthesis of anti-HIV and anti-tumour β-carbolines
Kusurkar, Radhika S.,Goswami, Shailesh K.
, p. 5315 - 5318 (2007/10/03)
Thermal electrocyclisation of the azahexatriene system has been used as a key step for the synthesis of anti-HIV and anti-tumour compounds, harman, derivatives of harman and 1-aryl-β-carbolines. A one-pot reaction sequence was used to furnish these compounds in good yield.
Efficient one-pot synthesis of anti HIV and antitumor compounds: Harman and substituted harmans
Kusurkar, Radhika S.,Goswami, Shailesh K.,Vyas, Sandhya M.
, p. 4761 - 4763 (2007/10/03)
Anti HIV and antitumor compounds, harman and substituted harmans have been synthesized using electrocyclization reactions as key steps. A one-pot reaction sequence was used to furnish these compounds in good overall yield.
