The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Formula: C10H12O2, 499-44-5, Name is Hinokitiol, SMILES is O=C1C(O)=CC(C(C)C)=CC=C1, in an article , author is Gu, Bo-Qi, once mentioned of 499-44-5.
Organocatalytic asymmetric synthesis of tetrahydrocarbazoles via an inverse-electron-demand Diels-Alder reaction of 2,3-indole-dienes with enals
A novel 2,3-indole-diene synthon was designed and synthesized, and was first applied to a stereoselective inverse-electron-demand Diels-Alder reaction to construct tetrahydrocarbazoles. In the presence of chiral secondary amines, a variety of enantioenriched, multifunctionalized tetrahydrocarbazole derivatives were obtained in good yields (up to 83%) with excellent stereoselectivities (up to >20:1 dr, 98% ee).
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 499-44-5, you can contact me at any time and look forward to more communication. Formula: C10H12O2.
Reference:
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles