62192-80-7

Upstream product

• 89-82-7 pulegone 
• 24302-23-6 (4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene 
• 67-56-1 methanol 
• 22472-80-6 syn-(-)-pulegol 
• 64-17-5 ethanol 
• 2385-77-5 (R)-Citronellal 
• 71-23-8 propan-1-ol 

Downstream Products

• 619-52-3 (1R)-menth-3-ene 
• 94348-42-2 (7S)-3,5,6,7,8,8a-hexahydro-4-methyl-1,2-benzodioxin-5-ol 
• 94348-40-0 mentha-4⁽⁵⁾,8⁽⁹⁾-dien-3-ol 
• 94425-40-8 3,5,6,7,8,8a-hexahydro-4,7-dimethyl-1,2-benzodioxin 
• 94425-39-5 3,5,6,7,8,8a-hexahydro-4,7-dimethyl-1,2-benzodioxin 
• 94348-41-1 mentha-4⁽⁵⁾,8⁽⁹⁾-dien-3-ol 

Relevant academic research and scientific papers

Acid-base catalyses by dimeric disilicoicosatungstates and divacant γ-Keggin-type silicodecatungstate parent: Reactivity of the polyoxometalate compounds controlled by step-by-step protonation of lacunary W{double bond, long}O sites

The catalytic properties of disilicoicosatungstates, [{γ-SiW10O32(H2O)2}2(μ-O)2]4- (2) and [H(γ-SiW10O32)2(μ-O)4]7- (3), and their parent divacant γ-Keggin type silicodecatungstate, [γ-SiW10O34(H2O)2]4- (1), toward C-C bond formation reactions have been investigated. The disilicoicosatungstate 2 with aquo ligands exhibits the acidic nature and catalyzes the Mukaiyama-aldol condensation and carbonyl-ene reaction, while 1 and 3 are rather basic and catalyze the Knoevenagel condensation. Therefore, the acid-base properties of a series of lacunary γ-Keggin silicotungstate derivatives 1-3 are clearly different, and the catalyses of 1-3 depend on the molecular structures while 1-3 are composed of a common [SiW10O32] fragment.

Reaction of allylic alcohols with aliphatic alcohols in the presence of cerium(III) chloride. Part II

The reactions of selected allylic alcohols with methanol, ethanol, n-propanol, isopropanol and tert-butanol in the presence of catalytic amounts of cerium(III) chloride are described. Allylic alkyl ethers, bis-allylic ethers and 1,3-dienes were obtained d

Microwave-Induced Reactions of Organic Substrates in the Cage of Zeolites

Microwave irradiation of compounds 1, 7, 15, 19, 23, and 24 adsorbed on Y zeolites has been studied.The reaction rate of the corresponding rearrangement, dehydrogenation and dehydration is dramatically enhanced as compared with reactions under thermal conditions.