690664-26-7Relevant academic research and scientific papers
One-Pot, Three-Step Synthesis of Benzoxazinones via Use of the Bpin Group as a Masked Nucleophile
Larin, Egor M.,Torelli, Alexa,Loup, Joachim,Lautens, Mark
supporting information, p. 2720 - 2725 (2021/04/05)
The utilization of the Bpin group as a pronucleophile to facilitate the assembly of cyclic carbamates has been achieved. This one-pot process involves an initial copper-catalyzed borylation, a subsequent C-B bond oxidation to generate the reactive alcohol
Design and application of intramolecular vinylogous Michael reaction for the construction of 2-alkenyl indoles
Harish, Battu,Yadav, Sanjay,Suresh, Surisetti
supporting information, p. 231 - 234 (2021/01/14)
A base-mediated transformation based on a designed intramolecular vinylogous Michael addition (intra-VMA) is presented to access 3-substituted 2-alkenyl indole derivatives. The reaction represents the first example of the intra-VMA for the construction of
[Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source
Liu, Yungen,Wei, Jinhu,Che, Chi-Ming
supporting information; experimental part, p. 6926 - 6928 (2010/11/16)
The syntheses of alkaloids including indoles, indolines, tetrahydroquinolines, dihydroquinazolinones and quinazolinones have been accomplished in moderate to excellent yields via [Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation using aryl azides as nitrogen source.
