Daniel H Ess
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Explore the profile of Daniel H Ess including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
Webber C, Kumawat J, Kong F, Dickie D, Ess D, Gunnoe T
Organometallics
. 2025 Mar;
44(5):617-627.
PMID: 40083949
The bis-acetate complexes (SbQ)Pt(OAc) () and (SbQPh)Pt(OAc) () (Q = 8-quinolinyl) were used to study C-Cl acetoxylation of 1,2-dichloroethane (DCE) to generate 2-chloroethyl acetate and the complexes (SbQ)PtCl () and...
2.
Irvankoski S, Davenport M, Ess D, Siitonen J
Chemistry
. 2025 Mar;
:e202403215.
PMID: 40034072
Blue light activation of N,N-dichlorocarbamates facilitates a direct 1,2-aminochlorination of unactivated olefins to yield 1,2-chloro-N-Cl compounds under ambient conditions. Mechanistic studies suggest that N,N-dichlorocarbamates undergo a photochemical excitation to yield...
3.
Yang B, Schaefer A, Small B, Leseberg J, Bischof S, Webster-Gardiner M, et al.
Chem Sci
. 2024 Oct;
PMID: 39449687
Linear α-olefins (1-alkenes) are critical comonomers for ethene copolymerization. A major impediment in the development of new homogeneous Fe catalysts for ethene oligomerization to produce comonomers and other important commercial...
4.
Webber C, Kong F, Kumawat J, Joy J, Richardson E, Siano P, et al.
Organometallics
. 2024 Sep;
43(17):1789-1802.
PMID: 39268180
A series of Pt-Sb complexes with two or three L-type quinoline side arms were prepared and studied. Two ligands, tri(8-quinolinyl)stibane (SbQ, Q = 8-quinolinyl, ) and 8,8'-(phenylstibanediyl)diquinoline (SbQPh, ), were...
5.
Rodriguez Trevino A, Loch-Temzelides P, Pandiri S, Kirkland J, Davenport M, Aguinaga U, et al.
Chem Sci
. 2024 Aug;
PMID: 39170719
The preparation of the β-lactam motif containing both C-Br and N-O bonds as functional handles remains an unmet synthetic challenge. Described herein is a novel and highly diastereoselective NBS-mediated cyclization...
6.
Luo J, Davenport M, Ess D, Leo Liu T
Angew Chem Int Ed Engl
. 2024 Jun;
63(38):e202407118.
PMID: 38849318
Cross-electrophile coupling (XEC) between aryl halides and alkyl halides is a streamlined approach for C(sp)-C(sp) bond construction, which is highly valuable in medicinal chemistry. Based on a key Ni aryl...
7.
Wheeler J, Schaefer A, Ess D
J Phys Chem A
. 2024 Jun;
128(24):4775-4786.
PMID: 38836889
Calculated potential energy structures and landscapes are very often used to define the sequence of reaction steps in an organometallic reaction mechanism and interpret kinetic isotope effect (KIE) measurements. Underlying...
8.
Schaefer A, Ess D
Phys Chem Chem Phys
. 2024 Apr;
26(15):11386-11394.
PMID: 38586933
In reactions with consecutive transition states without an intermediate, and an energy surface bifurcation, atomic motion generally determines product selectivity. Understanding this dynamic-based selectivity can be straightforward if there is...
9.
Luo J, Davenport M, Ess D, Leo Liu T
Angew Chem Int Ed Engl
. 2024 Mar;
63(22):e202403844.
PMID: 38518115
Paired redox-neutral electrolysis offers an attractive green platform for organic synthesis by avoiding sacrificial oxidants and reductants. Carboxylates are non-toxic, stable, inexpensive, and widely available, making them ideal nucleophiles for...
10.
Mpaata P, Miller C, Bonsrah D, Camp A, Ballard K, Angelie L, et al.
J Org Chem
. 2024 Mar;
89(6):3883-3893.
PMID: 38440874
Polycyclic aryl naphthalene and tetralin dihydro arylnaphthalene lactone lignans possess anticancer and antibiotic activity. Related furo[3,4-]pyranones, typified by the sequester-terpenoid isobolivianine, show similar antiproliferative bioactivity. Efficient syntheses of compounds featuring...