Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Radha Bam"'
Publikováno v:
Chemical Science. 12:1736-1744
Dehydrohalogenation, or elimination of hydrogen-halide equivalents, remains one of the simplest methods for the installation of the biologically-important olefin functionality. However, this transformation often requires harsh, strongly-basic conditi
Publikováno v:
Chemical Science
Dehydrohalogenation, or elimination of hydrogen-halide equivalents, remains one of the simplest methods for the installation of the biologically-important olefin functionality. However, this transformation often requires harsh, strongly-basic conditi
Autor:
Vincent J. Catalano, Sergio Abbate, Roberta Franzini, Matteo Tommasini, Radha Bam, Wesley A. Chalifoux, Claudio Villani, Giovanna Longhi, Marilyn M. Olmstead, Andrea Lucotti, Wenlong Yang
Publikováno v:
Organic Letters. 21:8652-8656
The synthesis of pyreno[a]pyrene-based helicene hybrids was achieved in good yield via a four-fold alkyne benzannulation reaction that was promoted by Bronsted acid. The molecules are configuration...
Publikováno v:
Angewandte Chemie. 130:14989-14993
The properties of nanographenes can be tuned by changing their shapes, therefore the development of new methods suitable for the synthesis of various nanographenes is highly desirable. Described herein is an intramolecular InCl3 /AgNTf2 -catalyzed re
Autor:
Radha Bam, Wesley A. Chalifoux
Publikováno v:
The Journal of Organic Chemistry. 83:9929-9938
A highly regioselective synthesis of 2,3-disubstituted chromen-4-one derivatives is accomplished from readily available internal alkynes and 2-methoxybenzoyl chlorides. The reaction proceeds via a domino intermolecular Friedel-Crafts acylation/intram
Autor:
Radha, Bam, Wenlong, Yang, Giovanna, Longhi, Sergio, Abbate, Andrea, Lucotti, Matteo, Tommasini, Roberta, Franzini, Claudio, Villani, Vincent J, Catalano, Marilyn M, Olmstead, Wesley A, Chalifoux
Publikováno v:
Organic letters. 21(21)
The synthesis of pyreno[
Publikováno v:
Synlett. 27:2161-2166
The development and utilization of highly functionalized and reactive dienophiles in the Diels–Alder cyclization reaction is of value in producing diversely functionalized, and therefore useful, cyclic products. We have developed a Diels–Alder re
Publikováno v:
Angewandte Chemie International Edition. 57:14658-14658
Publikováno v:
Angewandte Chemie. 130:14870-14870