Marek Figlus
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Explore the profile of Marek Figlus including associated specialties, affiliations and a list of published articles.
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9
Citations
15
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Recent Articles
1.
Matcha K, Chernichenko K, Jouvin K, Guduguntla S, Tran D, Bell S, et al.
J Org Chem
. 2022 Aug;
87(16):10736-10746.
PMID: 35921209
A palladium-catalyzed Heck reaction between 2-oxyacrylates and aryl bromides was developed, where DavePhos was a unique ligand that efficiently promoted the reaction. The products, 2-oxycinnamates, served as excellent precursors, providing...
2.
Figlus M, Wellaway N, Cooper A, Sollis S, Hartley R
ACS Comb Sci
. 2011 Mar;
13(3):280-5.
PMID: 21438502
Triphenylphosphine tagged with a short poly-(ethyleneglycol)-ω-monomethyl ether chain (light MPEG, 10−16 ethylenoxy units, (M)TPP-G2) and an MPEG-tagged version of diethyl azodicarboxylate ((M)DEAD) have been used to prepare a 20 member...
3.
Figlus M, Tarruella A, Messer A, Sollis S, Hartley R
Chem Commun (Camb)
. 2010 May;
46(24):4405-7.
PMID: 20473429
A toolkit of low molecular weight MPEG-supported coupling agents ((M)IIDQ, (M)EDCI), reagents for the Mitsunobu reaction ((M)DEAD, (M)TPP), an alternative to diazomethane, and scavengers can be used in the solution-phase...
4.
Figlus M, Caldwell S, Walas D, Yesilbag G, Cooke G, Kocovsky P, et al.
Org Biomol Chem
. 2009 Dec;
8(1):137-41.
PMID: 20024144
Asymmetric reduction of ketimines with trichlorosilane can be catalysed by the Lewis-basic N-methylvaline-derived formamide anchored to a soluble dendron () with good enantioselectivity (</=94% ee) and low catalyst loading (typically...
5.
Malkov A, Figlus M, Prestly M, Rabani G, Cooke G, Kocovsky P
Chemistry
. 2009 Aug;
15(38):9651-4.
PMID: 19711393
No abstract available.
6.
Malkov A, Figlus M, Cooke G, Caldwell S, Rabani G, Prestly M, et al.
Org Biomol Chem
. 2009 Jul;
7(9):1878-83.
PMID: 19590783
Gold nanoparticles functionalised with a valine-derived formamide have been developed as effective homogenous catalysts for the asymmetric reduction of ketimine 1 with trichlorosilane (< or = 84% ee) in toluene....
7.
Maslowska-Lipowicz I, Figlus M, Zuiderveld O, Walczynski K
Arch Pharm (Weinheim)
. 2008 Nov;
341(12):762-73.
PMID: 19009544
A series of 1-benzyl-4-(3-aminopropyloxy)piperidine and 1-benzyl-4-(5-aminopentyloxy)piperidine derivatives has been prepared. The 1-benzyl-4-hydroxypiperidine derivatives obtained were evaluated for their affinities at recombinant human histamine H(3 )receptor, stably expressed in HEK 293T...
8.
Malkov A, Figlus M, Kocovsky P
J Org Chem
. 2008 May;
73(11):3985-95.
PMID: 18444681
Asymmetric reduction of ketimines 1a-e with trichlorosilane can be catalyzed by the N-methylvaline-derived Lewis basic formamide anchored to a polymeric support (5a and 5b) with good enantioselectivity (< or =82%...
9.
Malkov A, Figlus M, Stoncius S, Kocovsky P
J Org Chem
. 2007 Feb;
72(4):1315-25.
PMID: 17288379
Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by N-methylvaline-derived Lewis-basic formamides 3a-d with high enantioselectivity (< or =95% ee) and low catalyst loading (1-5 mol %) at...