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1 xide, butylene oxide, isobutylene oxide, and cyclohexene oxide).
2 catalyst concentration and concentration of cyclohexene oxide.
3 , is only a weak Lewis acid, and polymerizes cyclohexene oxide.
4 catalyzed isomerization of cyclopentene- and cyclohexene oxides.
5 n of 17AAG with human hepatic microsomes and cyclohexene oxide, a known inhibitor of microsomal epoxi
8 be an effective catalyst for the coupling of cyclohexene oxide and carbon dioxide to afford poly(cycl
9 nesium catalysts for the copolymerization of cyclohexene oxide and carbon dioxide, active under just
12 A common reaction pathway for alicyclic (cyclohexene oxide) and aliphatic (propylene oxide) carbo
14 exene oxide, cyclopentane oxide, substituted cyclohexene oxide, and butylene oxide, each combined wit
15 zinc catalyst and a mixture of caprolactone, cyclohexene oxide, and carbon dioxide enables the select
16 together with biobased epsilon-decalactone, cyclohexene oxide, and carbon dioxide to make a series o
17 ethenation of benzene, the polymerization of cyclohexene oxide, and the oligomerization of ethene to
18 opolymer, poly(cyclohexene oxide-b-lactide-b-cyclohexene oxide-b-lactide), and an ABC triblock copoly
20 including an ABAB tetrablock copolymer, poly(cyclohexene oxide-b-lactide-b-cyclohexene oxide-b-lactid
22 a CO(2)-derived polycarbonate, poly(4-vinyl cyclohexene oxide carbonate), which provides mechanical
23 ocatalyst in the copolymerization of CO2 and cyclohexene oxide catalyzed by chromium salen derivative
24 he ring-opening copolymerizations (ROCOP) of cyclohexene oxide (CHO) and carbon dioxide (CO(2)), cond
29 rizations of (rac)-beta-butyrolactone (BBL), cyclohexene oxide (CHO), and carbon dioxide were realize
34 nium salts toward the photopolymerization of cyclohexene oxide depend on the counterion and the sulfo
36 of 2-cyclohexenone and 2-cycloheptenone open cyclohexene oxide in 60-62% yields and with 32-95:1 dias
37 nones nucleophilically open cyclopentene and cyclohexene oxides in 57-76% yields and with 4-8:1 diast
38 xides at ambient conditions, specifically to cyclohexene oxide, indicating that the structure of HPs
40 he reaction of carbon dioxide with epoxides (cyclohexene oxide or propylene oxide) using the (salen)C
41 of four model monomers-epsilon-caprolactone, cyclohexene oxide, phthalic anhydride, and carbon dioxid
42 locks and a flexible poly(tetrahydrofuran-co-cyclohexene oxide) (poly(THF-co-CHO) copolymer as the mi
44 a(5)-C(5)H(5)) was found to insert CO(2) and cyclohexene oxide, producing L(dipp)Al(Me)(mu:kappa(2)-O
45 d various epoxides (cyclohexene oxide, vinyl-cyclohexene oxide, propene oxide, allyl glycidyl ether)
47 f the copolymerization of carbon dioxide and cyclohexene oxide to produce poly(cyclohexene carbonate)
48 ter-phthalic anhydride and various epoxides (cyclohexene oxide, vinyl-cyclohexene oxide, propene oxid
49 ere synthesized via the terpolymerization of cyclohexene oxide with a mixture of CO(2) and COS in the
50 r 1 h, resulting in a 78% conversion to poly(cyclohexene oxide) with an average molecular weight (MW)