Zobrazeno 1 - 10
of 84
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
Publikováno v:
Frontiers in Surgery, Vol 11 (2024)
Recurrence of low-grade appendiceal pseudomyxoma peritonei (PMP) with splenic invasion and parastomal hernia is exceptionally rare. We present a 47-year-old female with recurrent PMP, four years post-cytoreductive surgery (CRS) and hyperthermic intra
Externí odkaz:
https://doaj.org/article/29fa0feb8a914b4a9df8e2a353a2dba4
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
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
Publikováno v:
Organic letters. 23(3)
A Lewis acid promoted intramolecular Schmidt reaction of
Publikováno v:
Chemical communications (Cambridge, England). 56(82)
A rhodium-catalyzed diastereo- and enantio-selective cyclopropanation of α-boryl styrenes with α-diazoarylacetates was established. Rh2(S-PTTL)4 (0.2 mol%) was found to be effective for the conversion, and 21 diastereopure cyclopropylboronates were
Publikováno v:
The Journal of Organic Chemistry. 83:5816-5824
A designed Tf2O-promoted intramolecular Schmidt reaction of 2-substituted ω-azido carboxylic acids was demonstrated. Tf2O was used as an activation reagent for the carboxylic acid, and ω-azido anhydride was in situ generated, releasing a molecular
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
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