Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Peiming, Gu"'
Publikováno v:
New Journal of Chemistry; 6/14/2024, Vol. 48 Issue 22, p9885-9889, 5p
Publikováno v:
Organic Letters. 23:1147-1151
A Lewis acid promoted intramolecular Schmidt reaction of N-acylbenzotriazoles with alkyl azides was designed and realized. The benzotriazole was not only employed as an efficient activator for initiating the Schmidt rearrangement but also used as a p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abc96a3a9f4d04676420223ec968c5f1
https://doi.org/10.1021/acs.orglett.1c00200
https://doi.org/10.1021/acs.orglett.1c00200
Publikováno v:
The Journal of Prosthetic Dentistry. 124:365-371
Statement of problem The presence of an anterior loop (AL), accessory mental foramen (AMF), or lateral lingual foramen (LLF) adds complexity to the mental foraminal region, and consequently, implant placement in this region can damage the nerves and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ab4e4b22a4e227b138bafb733c49304
https://doi.org/10.1016/j.prosdent.2019.06.026
https://doi.org/10.1016/j.prosdent.2019.06.026
Publikováno v:
The Journal of Organic Chemistry. 84:5813-5820
Rh-catalyzed intramolecular condensation of the benzyl azides with α-aryldiazoesters was explored. The reaction proceeded through the nucleophilic attack of the organic azide onto a rhodium carbenoid, while releasing nitrogen gas, affording the α-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb965cfa725106963b310f3084983783
https://doi.org/10.1021/acs.joc.8b03180
https://doi.org/10.1021/acs.joc.8b03180
Publikováno v:
Organic letters. 23(3)
A Lewis acid promoted intramolecular Schmidt reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f2b137cb87c23c545f8035f509a7343
https://pubmed.ncbi.nlm.nih.gov/33492975
https://pubmed.ncbi.nlm.nih.gov/33492975
Publikováno v:
Tetrahedron Letters. 59:2170-2172
An efficient synthesis of naturally occurring (R)-tylophorine is described. The alkaloid was prepared in seven steps from a known phenanthryl aldehyde with an overall yield of 14.2%. Asymmetric hydrogenation of an allyl alcohol was employed as a key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b25ba3ff4743f1dfbb3cfca66fc27166
https://doi.org/10.1016/j.tetlet.2018.04.052
https://doi.org/10.1016/j.tetlet.2018.04.052
Publikováno v:
The Journal of organic chemistry. 84(4)
The Schmidt reaction of ω-azido valeryl chlorides in the presence of an additional nucleophile was explored. The arenes, alcohols, and amines were demonstrated as the intermolecular trapping reagents for isocyanate ion and N-acyliminium ion from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80c456e155c7762df395b750e4c9fccd
https://pubmed.ncbi.nlm.nih.gov/30638022
https://pubmed.ncbi.nlm.nih.gov/30638022
Publikováno v:
Chinese Journal of Organic Chemistry. 40:2555
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7042b6db9b1aea3b26516594f89f8bd9
https://doi.org/10.6023/cjoc202003017
https://doi.org/10.6023/cjoc202003017
Publikováno v:
Tetrahedron Letters. 57:5666-5668
Asymmetric hydrogenation of 1-silyl-1-substituted alkenes has been explored, producing eight optically active silanes with good to excellent enantioselectivity (66–99% ee) and yield (74–99%). The reaction was efficiently catalyzed by the cationic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df0b8adbb4960dfa1fab1824a2260a03
https://doi.org/10.1016/j.tetlet.2016.11.017
https://doi.org/10.1016/j.tetlet.2016.11.017
Publikováno v:
The Journal of organic chemistry. 83(10)
A designed Tf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::007c62c79133d412eab29cc7e695c308
https://pubmed.ncbi.nlm.nih.gov/29667405
https://pubmed.ncbi.nlm.nih.gov/29667405