78604-93-0

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• 31401-28-2 4-(3,4-dihydro-1-naphthalenyl)morpholine 
• 31401-27-1 N-(3,4-dihydronaphthalen-1-yl)piperidine 
• 7007-34-3 1-(3,4-dihydro-1-naphthalenyl)pyrrolidine 
• 15424-14-3 N-phenylbenzohydrazonoyl chloride 
• 447-53-0 1,2-Dihydronaphthalene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 588-64-7 benzaldehyde phenylhydrazone 
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• 70563-82-5 methyl 3,4-dihydronaphthalene-1-carboxylate 
• 78604-87-2 (3aR,9bR)-1,3-Diphenyl-3a,4,5,9b-tetrahydro-1H-benzo[g]indazole 
• 78604-87-2 1,3-diphenyl 3a,4,5,9b-tetrahydrobenzo(g)indazole 
• 13148-18-0 3′‐phenyl‐3,4‐dihydro‐1H-spiro(naphthalene‐2,2’‐oxiran)‐1‐one 
• 100-63-0 phenylhydrazine 

Relevant academic research and scientific papers

Cycloaddition of Nitrile Imines with Enamides: An Approach to Functionalized Pyrazolines and Pyrazoles

An efficient [3 + 2] cycloaddition of in situ generated nitrile imines with enamides has been established. A wide range of functionalized pyrazoline derivatives (53 examples) were obtained in moderate to good yields (up to 96%) under very mild conditions. This protocol features broad substrate scope, good functional group tolerance, and operational simplicity. Practical transformation of the products into useful pyrazoles via a one-pot process and the scalability of this protocol highlight the utility of this synthetic methodology.

Corrigendum to “AlCl3-promoted reaction of cycloalkanones with hydrazones: A convenient direct synthesis of 4,5,6,7-tetrahydro-1H-indazoles and their analogues” (Tetrahedron Letters (2019) 60(35), (S0040403919307439), (10.1016/j.tetlet.2019.150988))

The authors regret that the printed version of the above article contained errors in Tables 1 and 2. A plausible mechanism was proposed using 1-benzylidene-2-phenylhydrazine 1a and cyclohexanone 2a as model reactants (Scheme 2). The formation of aluminum

AlCl3-promoted reaction of cycloalkanones with hydrazones: a convenient direct synthesis of 4,5,6,7-tetrahydro-1H-indazoles and their analogues

The AlCl3-promoted reactions of cycloalkanones with hydrazones are described. This approach represents a mild and operationally simple method to access 2,3-diaryl-4,5,6,7-tetrahydro-1H-indazoles and their analogues in good to moderate yields.

MODULATION DE LA REGIOSELECTIVITE LORS DE LA CYCLOADDITION DE LA DIPHENYLNITRILIMINE SUR DIVERS DIHYDRO-1,2 NAPHTALENES SUBSTITUES. STEREOSPECIFICITE DE LA REACTION

In order to control the regiochemistry of the cycloaddition of diphenylnitrilimine on 1,2-dihydronaphtalene and at-1 or -2 substituted derivatives and to obtain either regioisomer, we introduce a methoxycarbonyl group at the 4- or 3- position of the dipol

REGIOSELECTIVITY AND SPECIFICITY IN CYCLOADDITION OF DIPHENYLNITRILIMINE

Diphenylnitrilimine cycloaddition reactions on 1,2-dihydronaphtalenes are only regioselective.Use of 1- or 2-tetralones enamines as dipolarophiles allows to attain regiospecificity.