Two representative macrocyclic lactones with methoxysulfonyl side chain（5a and 5b）were synthesized employing Michael addition with acrolein and ring enlargement as the key steps,starting from potassium,α-oxocycloai...Two representative macrocyclic lactones with methoxysulfonyl side chain（5a and 5b）were synthesized employing Michael addition with acrolein and ring enlargement as the key steps,starting from potassium,α-oxocycloaikylsulfonates（1）in total yields of 45 and 57%,respectively.展开更多
The macrocyclic lactones building on calix[4]arenes 3a-b and double calix[4]arenes 4a-b were synthesized by the reaction of p-tert-butylcalix[4]arene (1a) or calix[4]arene (1b) with glycol bis(2-chloroacetate) (2). Th...The macrocyclic lactones building on calix[4]arenes 3a-b and double calix[4]arenes 4a-b were synthesized by the reaction of p-tert-butylcalix[4]arene (1a) or calix[4]arene (1b) with glycol bis(2-chloroacetate) (2). The conditions to improve the yields of double calix[4]arenes have been discussed.展开更多
The effects of the chain length and stereo-factor of substrates and solvents on the lipase catalysed lactonization of ω-hydroxy-ester were studied, And also the catalytic effects of various enzymes were compared.
文摘Two representative macrocyclic lactones with methoxysulfonyl side chain（5a and 5b）were synthesized employing Michael addition with acrolein and ring enlargement as the key steps,starting from potassium,α-oxocycloaikylsulfonates（1）in total yields of 45 and 57%,respectively.
文摘The macrocyclic lactones building on calix[4]arenes 3a-b and double calix[4]arenes 4a-b were synthesized by the reaction of p-tert-butylcalix[4]arene (1a) or calix[4]arene (1b) with glycol bis(2-chloroacetate) (2). The conditions to improve the yields of double calix[4]arenes have been discussed.
文摘The effects of the chain length and stereo-factor of substrates and solvents on the lipase catalysed lactonization of ω-hydroxy-ester were studied, And also the catalytic effects of various enzymes were compared.
