Robert J Halter
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Explore the profile of Robert J Halter including associated specialties, affiliations and a list of published articles.
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7
Citations
218
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Recent Articles
1.
Bowling N, Burrmann N, Halter R, Hodges J, McMahon R
J Org Chem
. 2010 Sep;
75(19):6382-90.
PMID: 20812705
A variety of substituted pentadiynols, -diynals, and -diynones have been prepared en route to precursors to dialkynyl carbenes (R(1)-C≡C-C-C≡C-R(2)). In light of the marginal stability associated with these simple systems,...
2.
Ihle N, Lemos R, Schwartz D, Oh J, Halter R, Wipf P, et al.
Mol Cancer Ther
. 2009 Jan;
8(1):94-100.
PMID: 19139117
The phosphatidylinositol 3-kinase (PI3K)/Akt signaling cascade is an important component of the insulin signaling in normal tissues leading to glucose uptake and homeostasis and for cell survival signaling in cancer...
3.
Wakefield B, Halter R, Wipf P
Org Lett
. 2007 Jul;
9(16):3121-4.
PMID: 17630756
The synthesis of a thiophene-containing analogue of halenaquinone was realized. Key steps include an alkynyl ketone-benzocyclobutane Diels-Alder reaction to construct the C,D-ring naphthalene subunit, a Heck cyclization to form the...
4.
Bowling N, Halter R, Hodges J, Seburg R, Thomas P, Simmons C, et al.
J Am Chem Soc
. 2006 Mar;
128(10):3291-302.
PMID: 16522111
1-Diazo-2,4-pentadiyne (6a), along with both monodeuterio isotopomers 6b and 6c, has been synthesized via a route that proceeds through diacetylene, 2,4-pentadiynal, and 2,4-pentadiynal tosylhydrazone. Photolysis of diazo compounds 6a-c (lambda...
5.
Wipf P, Halter R
Org Biomol Chem
. 2005 May;
3(11):2053-61.
PMID: 15917886
Recent synthetic and biological studies of the viridin class of steroidal furans have revealed multiple opportunities for fundamental discoveries as well as advanced drug design. Wortmannin is a potent enzyme...
6.
Ihle N, Williams R, Chow S, Chew W, Berggren M, Paine-Murrieta G, et al.
Mol Cancer Ther
. 2004 Jul;
3(7):763-72.
PMID: 15252137
We have developed biologically stable semisynthetic viridins as inhibitors of phosphoinositide (PtdIns)-3-kinases. The most active compound was PX-866 (acetic acid (1S,4E,10R,11R,13S,14R)-[4-diallylaminomethylene-6-hydroxy-1-methoxymethyl-10,13-dimethyl-3,7,17-trioxo-1,3,4,7,10,11,12,13,14,15,16,17-dodecahydro-2-oxa-cyclopenta[a]phenanthren-11-yl ester), which inhibited purified PtdIns-3-kinase with an IC50 of...
7.
Wipf P, Minion D, Halter R, Berggren M, Ho C, Chiang G, et al.
Org Biomol Chem
. 2004 Jul;
2(13):1911-20.
PMID: 15227545
A series of viridin analogs was prepared from wortmannin by nucleophilic ring opening at C(20) and evaluated against the signaling kinases PI-3-kinase and mTOR. Several subnanomolar enzyme inhibitors with orders...