Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Fanji Kong"'
Publikováno v:
In Heliyon August 2023 9(8)
Autor:
Fanji Kong, Shusen Chen, Junqi Chen, Chang Liu, Weihao Zhu, Diane A. Dickie, William L. Schinski, Sen Zhang, Daniel H. Ess, T. Brent Gunnoe
Publikováno v:
Science advances. 8(34)
We report carbon-hydrogen acetoxylation of nondirected arenes benzene and toluene, as well as related functionalization with pivalate and 2-ethylhexanoate ester groups, using simple copper(II) [Cu(II)] salts with over 80% yield. By changing the ratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d90959a521a38b136a994efd26767095
https://pubmed.ncbi.nlm.nih.gov/36001664
https://pubmed.ncbi.nlm.nih.gov/36001664
Publikováno v:
2nd International Conference on Mechanical, Electronics, and Electrical and Automation Control (METMS 2022).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a7d0eb14ff12fb1619ee67990e0ec14
https://doi.org/10.1117/12.2634907
https://doi.org/10.1117/12.2634907
Publikováno v:
Organometallics. 39:3918-3935
Hydrogen–deuterium exchange (H/D exchange) is a method commonly used for studying catalytic activation of C–H(D) bonds by transition metal complexes. In this study, a series of additives were studi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6372ef2c87acada6f0669a1aecb6a9ec
https://doi.org/10.1021/acs.organomet.0c00623
https://doi.org/10.1021/acs.organomet.0c00623
Autor:
Fanji Kong1, Shusen Chen2, Junqi Chen1, Chang Liu1, Weihao Zhu1, Dickie, Diane A.1, Schinski, William L.3, Sen Zhang1, Ess, Daniel H.2 dhe@chem.byu.edu, Gunnoe, T. Brent1 tbg7h@virginia.edu
Publikováno v:
Science Advances. 8/26/2022, Vol. 8 Issue 34, p1-14. 14p.
Autor:
LeGrande Slaughter, Vladimir Nesterov, Sachin Handa, Fanji Kong, John Nguyen, matthew ellison, Aaron Ruch
Two series of sterically encumbered gold(I)-acyclic diaminocarbene (ADC) complexes were prepared by reaction of mono- and dialkylamines with gold-bound 2-mesitylphenyl isocyanide (monomesityl series) and 2,6-dimesitylphenyl isocyanide (dimesityl seri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f908eb331893507eb5ce8f16d852fff1
https://doi.org/10.26434/chemrxiv.13338116
https://doi.org/10.26434/chemrxiv.13338116
Autor:
Matthew C. Ellison, LeGrande M. Slaughter, Aaron A. Ruch, John K. Nguyen, Sachin Handa, Fanji Kong, Vladimir N. Nesterov
Two series of sterically encumbered gold(I)-acyclic diaminocarbene (ADC) complexes were prepared by reaction of mono- and dialkylamines with gold-bound 2-mesitylphenyl isocyanide (monomesityl series) and 2,6-dimesitylphenyl isocyanide (dimesityl seri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc2f13b0b2e05c824193c39133ea06ef
https://doi.org/10.26434/chemrxiv.13338116.v1
https://doi.org/10.26434/chemrxiv.13338116.v1
Autor:
Dale R. Pahls, LeGrande M. Slaughter, Aaron A. Ruch, Sachin Handa, Thomas R. Cundari, Vladimir N. Nesterov, Fanji Kong
Publikováno v:
Organicbiomolecular chemistry. 14(34)
A Pd(OAc)2/xantphos catalyst system was found effective for benzylaminations of binaphthyl 2-triflates bearing a variety of alkyl, benzyl, and substituted phenyl substituents at the 2′-position. With 2′-aryl substituents, an intramolecular Pd-cat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b9fe921e28495db970850337d38b998
https://pubmed.ncbi.nlm.nih.gov/27507596
https://pubmed.ncbi.nlm.nih.gov/27507596
Publikováno v:
ChemInform. 44
A tandem reaction initiated by Au(I)-catalyzed C1—C5 cyclization of enediynes (I) and (III) bearing an internal carboxy nucleophile is developed, providing a novel route for the assembly of fused indene derivatives (II) and (IV).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dc2785a587d00466f27ed1f1698655f
https://doi.org/10.1002/chin.201320155
https://doi.org/10.1002/chin.201320155
Publikováno v:
ChemInform. 44
The reaction conditions (silver-free) are optimized for the preparation of the alkaloid scaffolds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ae0a3f6bae964f4ecea27475bf272c9
https://doi.org/10.1002/chin.201315154
https://doi.org/10.1002/chin.201315154