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Joseph L Howard

Explore the profile of Joseph L Howard including associated specialties, affiliations and a list of published articles. Areas
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Articles 6
Citations 198
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Recent Articles
1.
Nicholson W, Howard J, Magri G, Seastram A, Khan A, Bolt R, et al.
Angew Chem Int Ed Engl . 2021 Aug; 60(43):23128-23133. PMID: 34405513
Efforts to generate organomanganese reagents under ball-milling conditions have led to the serendipitous discovery that manganese metal can mediate the reductive dimerization of arylidene malonates. The newly uncovered process has...
2.
Howard J, Brand M, Browne D
Angew Chem Int Ed Engl . 2018 Oct; 57(49):16104-16108. PMID: 30335216
A reaction manifold has been discovered in which the chemoselectivity can be altered by switching between neat milling and liquid assisted grinding (LAG) with polar additives. After investigation of the...
3.
Cao Q, Howard J, Wheatley E, Browne D
Angew Chem Int Ed Engl . 2018 Jul; 57(35):11339-11343. PMID: 30015403
A form independent activation of zinc, concomitant generation of organozinc species and engagement in a Negishi cross-coupling reaction via mechanochemical methods is reported. The reported method exhibits a broad substrate...
4.
Howard J, Cao Q, Browne D
Chem Sci . 2018 May; 9(12):3080-3094. PMID: 29780455
Mechanochemistry is becoming more widespread as a technique for molecular synthesis with new mechanochemical reactions being discovered at increasing frequency. Whilst mechanochemical methods are solvent free and can therefore lead...
5.
Howard J, Nicholson W, Sagatov Y, Browne D
Beilstein J Org Chem . 2017 Oct; 13:1950-1956. PMID: 29062413
Solventless mechanochemical synthesis represents a technique with improved sustainability metrics compared to solvent-based processes. Herein, we describe a methodical process to run one solventless reaction directly into another through multistep...
6.
Howard J, Schotten C, Alston S, Browne D
Chem Commun (Camb) . 2016 Jun; 52(54):8448-51. PMID: 27306975
We report an operationally simple, metal-free approach for the late-stage introduction of the important lipophilic hydrogen-bond donor motif, SCF2H. This reaction converts diaryl- and dialkyl-disulfides into the corresponding aryl/alkyl-SCF2H through...