74607-02-6

Upstream product

• 51867-06-2 1-benzoyl-1,2,2a,3-tetrahydrobenzindol-4-(5H)-one 
• 74-89-5 methylamine 

Downstream Products

• 74607-00-4 4-benzoyl-5,5a,6,8,9,10-hexahydroindolo<4,3-fg>quinolin-8(4H)-one 
• 74607-01-5 4-benzoyl-5,5a,6,8,9,10-hexahydro-9-methylindolo<4,3-fg>quinolin-8(4H)-one 
• 68017-67-4 4-benzoyl-5,5a,6,8,9,10-hexahydro-7-methylindolo<4,3-fg>quinolin-8(4H)-one 
• 100999-20-0 (+/-)-trans-4,6,6a,7,8,12b-hexahydro-7-methylindolo<4,3-ab>phenanthridine 
• 61361-26-0 4-benzoyl-5,5a,6,8,9,10-hexahydro-7,9-dimethylindolo<4,3-fg>quinolin-8(4H)-one 
• 436-41-9 festuclavine 
• 436-41-9 (+/-)-costaclavine 
• 436-41-9 (+/-)-epi-costaclavine 
• 61361-25-9 1-benzoyl-1,2,2a,3-tetrahydro-4-(N-methyl-2-methylacrylamido)benzindole 
• 100999-19-7 1,N-dibenzoyl-4-(methylamino)-1,2,2a,3-tetrahydrobenzindole 

Relevant academic research and scientific papers

trans-Hexahydroindolophenanthridines ("Benzergolines"), the First Structural Class of Potent and Selective Dopamine D1 Receptor Agonists Lacking a Catechol Group

In contrast to the many selective dopamine (DA) D2 receptor agonists known, only two prototypes of selective D1 receptor agonists have been described; both show preference for the periphery due to their catechol partial structures.Ou

Photocyclisation of Enamides. Part 16. A New Synthesis of Clavines. The Stereostructure of Costaclavine

Epimeric 6,8-dimethylergolines (VI), (VII), and (IX) have been synthesised from the lactam (IVa) which was prepared by the reaction of the enamine (II) with methacryloyl chloride or methacrylamide.The stereochemistry of costaclavine (VI) has been establis