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1 entgegen or zusammen orientations of the two allyl groups.
2 a variety of cyclic or acyclic disubstituted allyl groups.
3 ed through-space interaction between the two allyl groups.
4 ng through-bond interactions between the two allyl groups.
5 in preference to less sterically encumbered allyl groups.
6 avior of magnolol and honokiol is due to the allyl groups.
7 ng tetraethylene glycol chains terminated by allyl groups.
8 <10 microL), a (1)H-(13)C HETCOR spectrum of allyl groups (AL, -CH(2)-CH=CH(2)) covalently anchored t
9 nd allows for the installation of the parent allyl group as well as a range of 2-substituted allylic
11 nd nitro groups, as well as benzyl group and allyl group deprotection under mild, neutral conditions.
12 3-Iodobenzoylnaloxamide 15 (IBNalA) with a N-allyl group displayed lower delta opioid receptor affini
15 volving Claisen rearrangement to transfer an allyl group from the C-7 hydroxyl of noreugenin to C-8 r
16 , two, and three ethylene glycol units to an allyl group have been investigated for chemoselectivity,
18 effects on affinity of an n-propyl and an n-allyl group in the new analogues of 3 and 4 suggest that
23 ctionalizable moieties, such as propargyl or allyl groups, into acyclic alpha,beta,gamma,delta-doubly
24 titatively by irradiation at 355 nm, and the allyl group is rapidly and efficiently removed by using
26 roach allowed for the elaboration of the 6-O-allyl group of highly functionalized macrolides at vario
27 e introduction of substituents at C-2 of the allyl group of O(6)-allylguanine reduced activity compar
33 ditions of propargyl and 2-boryl-substituted allyl groups to acyclic dienoates with high selectivity.
34 quence for the formal two-carbon scission of allyl groups to carboxylic acids has been developed.
36 nd and the fluorophore was photocleaved, the allyl group was removed by using a Pd-catalyzed reaction
37 -allyl derivatives of (+)-catechin, and this allyl group was used in a series of cross-metathesis exp
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