Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Scott V. Plummer"'
Autor:
Uyen T. Duong, Scott V. Plummer, Tharique N. Ansari, Sachin Handa, Fabrice Gallou, Pawel M. Kozlowski, Sudripet Sharma, Jacek B. Jasinski, Saurav Parmar
Publikováno v:
ACS Sustainable Chemistry & Engineering. 9:2854-2860
Upon visible-light irradiation, the heterogeneous polymer of PDI–Cu(I)–PDI (PDI = perylene diimide) generates charge transfer states that are subsequently quenched by molecular oxygen for their par...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9df9821bc9c8dbf0de552a3623be3cb3
https://doi.org/10.1021/acssuschemeng.0c08792
https://doi.org/10.1021/acssuschemeng.0c08792
Autor:
Jim Yuchen Chang, Scott V. Plummer, Fabrice Gallou, Richard I. Robinson, Bruce H. Lipshutz, Alex B. Wood, Marie Smith
Publikováno v:
Green Chemistry. 23:7724-7730
Herein are reported initial efforts to develop a generally accessible flow process, applying a heterogenous nanocatalyst to aqueous micelle-enabled Suzuki–Miyaura coupling reactions. Also disclosed is a new engineering solution (i.e., a self-draini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f690e18f97ade722995d3724bf22d541
https://doi.org/10.1039/d1gc02461b
https://doi.org/10.1039/d1gc02461b
Publikováno v:
ACS Catalysis. 9:10963-10970
Palladium nanoparticles ligated with inexpensive triphenylphosphine and amphiphile PS-750-M are suitable for exploring the reactivity of carbenes in aqueous nanomicelles. Nanocatalyst is highly sel...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e75337d769a663002b978ade2b351567
https://doi.org/10.1021/acscatal.9b04175
https://doi.org/10.1021/acscatal.9b04175
Autor:
Helen F. Sneddon, Frank Roschangar, Sudhir Nambiar, Seth D. Ribe, Jeremy P. Scott, Michael E. Kopach, Scott V. Plummer, Guy R. Humphrey, Juan Colberg, Alina Borovika, Christiana Briddell, Isamir Martinez, Cisco Bee, Stefan G. Koenig
Publikováno v:
ACS Sustainable Chemistry & Engineering. 7:16937-16951
In an effort to improve sustainability and reduce the cost of goods for active pharmaceutical ingredients (APIs), pharma companies have partnered on varying portions of their supply chain with cont...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84afb2c0f74a6c1b1faa69c220f1e00b
https://doi.org/10.1021/acssuschemeng.9b02842
https://doi.org/10.1021/acssuschemeng.9b02842
Autor:
Sachin Handa, Adam H. Clark, Fabrice Gallou, Tharique N. Ansari, Armand Taussat, Maarten Nachtegaal, Scott V. Plummer
Publikováno v:
ACS Catalysis. 9:10389-10397
A nanocatalyst for micellar Buchwald–Hartwig aminations is developed, thoroughly characterized, and applied on a variety of substrates. The catalyst is stable under ambient conditions for at least ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e157391daf811e86520c4f5c545b3c94
https://doi.org/10.1021/acscatal.9b02622
https://doi.org/10.1021/acscatal.9b02622
Autor:
Jacek B. Jasinski, Pranjal P. Bora, Sachin Handa, Fabrice Gallou, Scott V. Plummer, Maarten Nachtegaal, Manisha Bihani
Publikováno v:
ACS Catalysis. 9:7520-7526
Both Ni(0) complexes and nanoparticles (NPs) are unstable in water, which poses a significant hindrance to their application in aqueous synthetic catalysis. To overcome these barriers, ligated Ni(0...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9313377b546c2b2be6c43c4bdd819cdd
https://doi.org/10.1021/acscatal.9b02316
https://doi.org/10.1021/acscatal.9b02316
Publikováno v:
ChemSusChem. 12(13)
Highly selective direct monofluorination of indoles and arenes was developed through an approach that allows site-specific solubility of substrate and fluorine source in the micelle. This approach was highly selective for a broad range of substrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63147ba57cf20dc949c947eb9c0c9ff1
https://pubmed.ncbi.nlm.nih.gov/30834700
https://pubmed.ncbi.nlm.nih.gov/30834700
Publikováno v:
Tetrahedron. 67:5083-5097
Strategies for the stereocontrolled preparations of 2,6-cis- and 2,6-trans-substituted tetrahydropyrans have been devised. These studies have explored methodology for asymmetric induction in SE′ reactions using chiral 1,3,2-diazaborolidine controll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e89c1943447aedb37b07a197edf0d71
https://doi.org/10.1016/j.tet.2011.05.020
https://doi.org/10.1016/j.tet.2011.05.020
Publikováno v:
Organic Letters. 5:5035-5038
A convergent, second generation formal synthesis of (+)-Leucascandrolide A (1) has been efficiently achieved by providing a flexible, enantiocontrolled strategy toward the bioactive macrolactone component. Advancements for stereocontrol in asymmetric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5064df616ceedcc31e11142bc3748f7e
https://doi.org/10.1021/ol036071v
https://doi.org/10.1021/ol036071v
Publikováno v:
Organic Letters. 3:1383-1386
[reaction in text] A convergent asymmetric synthesis of (-)-ratjadone (1) has been achieved, confirming the assignments of stereochemistry for the naturally occurring antifungal metabolite.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22b593e7916c5f92241430c7f6423cf9
https://doi.org/10.1021/ol015753k
https://doi.org/10.1021/ol015753k