Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yi-Tan Su"'
Publikováno v:
Organic Chemistry Frontiers. 9:2739-2745
The palladium-catalyzed three-component 1,4-aminoarylation of [60]fullerene afforded 1,4-(aryl)(sulfonamide)[60]fullerenes, of which the sulfonamide group could be replaced by a (hetero)aryl, malonate ester or allyl group in the presence of FeCl3.
Publikováno v:
Journal of Organic Chemistry; 3/18/2022, Vol. 87 Issue 6, p4051-4060, 10p
Publikováno v:
Chemical Communications. 51:6548-6551
A cuprous bromide-catalyzed heteroannulation reaction of [60]fullerene with ketoxime acetates has been exploited to prepare novel 1-fulleropyrrolines through the cleavage of N-O and C-H bonds and formation of C-C and C-N bonds under thermal condition
Publikováno v:
Org. Chem. Front.. 1:689-693
The palladium-catalyzed heteroannulation of [60]fullerene with various N-(2-arylethyl) sulfonamides afforded a variety of [60]fullerene-fused tetrahydrobenzazepines. These reactions were initiated by C–H bond activation and followed by cyclization.
Publikováno v:
ChemInform. 46
Novel 1-fulleropyrrolines are synthesized by a copper bromide-catalyzed heteroannulation reaction of [60]fullerene with ketoxime acetates through the cleavage of N—O and C—H bonds and formation of C—C and C—N bonds under thermal conditions.
Autor:
Guan-Wu Wang, Yi-Tan Su
Publikováno v:
Organic letters. 15(13)
The FeCl3-mediated reaction of [60]fullerene with N-benzhydryl sulfonamides afforded C60-fused indane derivatives using the high-speed vibration milling technique. A possible reaction mechanism involving the unprecedented FeCl3-mediated homolytic C
Publikováno v:
Chemical communications (Cambridge, England). 48(65)
The palladium-catalysed heteroannulation of [60]fullerene with various N-benzyl sulfonamides via C–H bond activation affords [60]fullerene-fused tetrahydroisoquinolines. In the presence of a Bronsted acid [60]fullerene-fused tetrahydroisoquinolines