Results
1 -
10 of
40
(Click
here to explore results)
- Probing the reactivity of o-phthalaldehydic acid/methyl ester: synthesis of N-isoindolinones and 3-arylaminophthalides. Sreeman K. Mamidyala, Matthew A. Cooper
, Chem. Commun.
, 2013
, 49
, 8407
- Fluoride-catalyzed nucleophilic addition of PhSCF2SiMe3 to anhydrides: synthesis of γ-difluoromethylated γ-lactams. Vannapha Pharikronburee, Teerachai Punirun, Darunee Soorukram, Chutima Kuhakarn, Patoomratana Tuchinda, Vichai Reutrakul, Manat Pohmakotr
, Org. Biomol. Chem.
, 2013
, 11
, 2022
- A new [4 + 1]/[4 + 2]bicycliaztion strategy for accessing functionalized indeno[1,2-b]pyran-2-ones. Bo Jiang, Rong Fu, Jiang-Kai Qiu, Yan Yu, Shu-Liang Wang, Shu-Jiang Tu
, RSC Adv.
, 2016
, 6
, 74372
- Pd-Catalyzed carbonylative lactonization of 2-halidearomatic aldehydes with H2O as a nucleophile. Min Si, Jiaqi Yan, Yongzheng Ding, Hanmin Huang
, Org. Biomol. Chem.
, 2022
, 20
, 3917
- Chiral organophosphates as ligands in asymmetric metal catalysis. Nikolai Brodt, Jochen Niemeyer
, Org. Chem. Front.
, 2023
, 10
, 3080
- p-Toluenesulfonic acid-promoted organic transformations for the generation of molecular complexity. Sanchari Pal, Debjit Das, Sabyasachi Bhunia
, Org. Biomol. Chem.
, 2024
, 22
, 1527
- CCLXIV.—The chlorination and bromination of the toluic acids and the preparation of the phthalaldehydic acids. William Davies, William Henry Perkin
, J. Chem. Soc., Trans.
, 1922
, 121
, 2202
- Synthesis of dihydroisoindolo[2,1-a]quinolin-11-ones, their in silico ADMET properties and in vitro antitumor activities. Diego R. Merchán-Arenas, Felipe Sojo, Francisco Arvelo, Vladimir V. Kouznetsov
, RSC Adv.
, 2020
, 10
, 42287
- Heterocyclic nitrogen compounds. Part IV. Further condensations with aldehydic acids and diamines. E. F. M. Stephenson
, J. Chem. Soc.
, 1954
, 2354
- 40. Heterocyclic nitrogen compounds. Part II. The preparation of 5 : 7 : 12 : 14-tetrahydro-6 : 13-diazanaphthacene and some derivatives thereof, with an example of ring expansion and contraction in a clemmensen reduction. H. H. Hatt, E. F. M. Stephenson
, J. Chem. Soc.
, 1952
, 199