ライフサイエンスコーパス: acetate ester

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1 all multiply unsaturated 10-22-carbon chain acetate esters.

2 masked as benzyl ethers and O-sulfonates as acetate esters.

3 d to the corresponding ketones, alcohols, or acetate esters.

4 plex mixture of volatiles including multiple acetate esters.

5 Base mediated macrocyclization of the acetate ester 16 followed by base mediated alkylation an

6 inc and alpha-bromoacetonitrile, alpha-bromo acetate esters, allyl bromide, benzyl bromide and alpha-

7 The opposite was observed among fusel acetate esters and 4-vinylguaiacol.

8 resence of cyclic carbamate, lactone, ketal, acetate ester, and epimerizable methyl ketone functional

9 ng taxa-4(20),11(12)-dien-5 alpha-ol and its acetate ester as test substrates.

10 hich 3' and 6' hydroxyl groups are masked as acetate esters (CFDA).

11 For commonly used 14-carbon chains with an acetate ester functional group, and 1-3 unsaturations, t

12 tle ageing were hydrolysis of 3MHA and other acetate esters, hydrolysis of ethyl esters of fatty acid

13 clade accumulate a relatively low content of acetate esters in comparison with the green-fruited spec

14 v) that dramatically decreased the amount of acetate esters in their pheromone glands (low-OAc).

15 Using model (R)-2-acetyl-2-phenyl acetate esters of (S)- or (R)-alpha-substituted-p-hydrox

16 art) suggests that the exocyclic C-O bond in acetate esters of cyclic alcohols intrinsically prefers

17 purogenum has substrate specificities toward acetate esters of d-xylopyranose residues in xylan and b

18 s, the majority being alcohols, aldehydes or acetate esters of olefinic chains of 10-22 carbons.

19 The results show that for acetate esters there are only seven or nine monounsatura

20 rene oxide to provide the corresponding diol acetate ester was studied with and without general-acid

21 The production of acetate esters was enhanced by mid-range ammonium supple

22 One exception was the 11beta-acetate esters where increasing the alcohol moiety from

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