669081-18-9

Upstream product

• 93-97-0 benzoic acid anhydride 
• 409305-55-1 (4S,1'S)-3-(1'-allyl-1'-phenylmethylamino)-4-phenylmethyl-2-oxazolidinone 
• 299216-18-5 (S)-3-(benzylidene)amino-4-phenylmethyl-2-oxazolidinone 
• 299216-13-0 (S)-3-amino-4-benzyl-1,3-oxazolan-2-one 
• 100-52-7 benzaldehyde 

Relevant academic research and scientific papers

Trifluoroacetyl-Activated Nitrogen-Nitrogen Bond Cleavage of Hydrazines by Samarium(II) Iodide

(Matrix presented) Trifluoroacetyl derivatives of hydrazines undergo clean and efficient reductive cleavage of the N-N bond with Sml2 in the presence of MeOH. After N-trifluoroacetylation, acyl-, aryl-, and alkyl-substituted hydrazines are redu

Asymmetric allylsilane additions to enantiopure N-acylhydrazones with dual activation by fluoride and In(OTF)3

A mild, convenient, and stereoselective addition of allylsilanes to enantiopure N-acylhydrazones occurs at room temperature upon complementary activation of both the allylsilane and the hydrazone (see scheme; OTf = trifluoromethanesulfonate). The reaction