1141822-49-2

Downstream Products

• 1141822-61-8 (1R,2S,5R)-8-phenylmenthyl (2R,4S,7S)-4-benzyl-2,7-dimethyl-5-oxooxepane-4-carboxylate 
• 1141822-59-4 (1R,2S,5R)-8-phenylmenthyl (1R,4R,6S)-1-benzyl-4,6-dimethyl-2-oxocycloheptanecarboxylate 
• 1141822-53-8 (1R,2S,5R)-8-phenylmenthyl (R)-1-benzyl-2-oxocycloheptanecarboxylate 
• 1141822-57-2 (1R,2S,5R)-8-phenylmenthyl (1R,5S)-1-benzyl-5-methyl-2-oxo-5-(trimethylsilyloxy)cycloheptanecarboxylate 
• 1141822-55-0 (1R,2S,5R)-8-phenylmenthyl (1R,5S)-1-benzyl-5-tert-butyl-2-oxocycloheptanecarboxylate 

Relevant academic research and scientific papers

Stereoselective construction of seven-membered rings with an all-carbon quaternary center by direct tiffeneau-demjanov-type ring expansion

Insertion of one methylene unit into the C-C bond of cyclohexanones is apotentially useful, straightforward method for the construction of seve n-membered carbocycles. An especially appealing but largely unexplored method in this arena is the nucleophilic