L A Paquette
Overview
Explore the profile of L A Paquette including associated specialties, affiliations and a list of published articles.
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Articles
37
Citations
60
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Recent Articles
1.
2.
Paquette L, Dressel J, Chasey K
J Am Chem Soc
. 2011 Dec;
108(3):512-4.
PMID: 22175475
No abstract available.
3.
Paquette L, Ross R, Springer J
J Am Chem Soc
. 2011 Dec;
110(18):6192-204.
PMID: 22148799
No abstract available.
4.
Cagide E, Louzao M, Espina B, Ares I, Vieytes M, Sasaki M, et al.
Chem Res Toxicol
. 2011 Apr;
24(6):835-42.
PMID: 21517028
Many microalgae produce compounds that exhibit potent biological activities. Ingestion of marine organisms contaminated with those toxins results in seafood poisonings. In many cases, the lack of toxic material turns...
5.
Paquette L
Chem Rec
. 2002 Mar;
1(4):311-20.
PMID: 11893071
The structural designation A originally made by Sharma and Alam to sclerophytin A was considered to be ambiguous and so notably strained relative to B that the latter was targeted...
6.
Paquette L, Owen D, Bibart R, Seekamp C
Org Lett
. 2001 Dec;
3(25):4043-5.
PMID: 11735580
[reaction: see text] The first spirocyclic nucleoside featuring a beta-hydroxyl (anti) at C5' has yielded to synthesis. While the OMOM functionality proved to be sensitive to the conditions necessary to...
7.
Paquette L, Bibart R, Seekamp C, Kahane A
Org Lett
. 2001 Dec;
3(25):4039-41.
PMID: 11735579
[reaction: see text] The potential benefits associated with the spirocyclic restriction of nucleosides are summarized. Following exploration of a pi-allylpalladium route to 5'-alpha- or syn-dideoxy examples, we evaluated MOM protection...
8.
Paquette L, Ra C, Gallucci J, Kang H, Ohmori N, Arrington M, et al.
J Org Chem
. 2001 Dec;
66(25):8629-39.
PMID: 11735548
The structural features most conducive to complexation of the alkali metal ions Li(+), Na(+), and K(+) in a series of constrained inositol orthoformate derivatives have been probed in solution, in...
9.
Balskus E, Arbit R, Paquette L
J Org Chem
. 2001 Oct;
66(20):6695-704.
PMID: 11578223
The reaction of open-chain or cyclic alpha-diketones with specific omega-alkenyl organometallics leads readily under the proper conditions to 1,2-diols bonded to terminal olefinic chains. With 1-phenyl-1,2-propanedione, biacetyl, and cyclohexane-1,2-dione, allylindation...
10.
Bernardelli P, Moradei O, Friedrich D, Yang J, Gallou F, Dyck B, et al.
J Am Chem Soc
. 2001 Sep;
123(37):9021-32.
PMID: 11552810
An enantioselective synthetic route to the thermodynamically most stable diastereomer of the structure assigned to sclerophytin A (5) has been realized. The required tricyclic ketone 33 was prepared by sequential...