Results 81 to 90 of about 865,390 (142)

Electrochemical oxidative rearrangement of tetrahydro-β-carbolines in a zero-gap flow cell. [PDF]

Chem Sci, 2022
Zheng Y, Cheung YT, Liang L, Qiu H, Zhang L, Tsang A, Chen Q, Tong R.   +7 more
europepmc   +1 more source

Synthesis, Molecular Docking and Antiplasmodial Activities of New Tetrahydro-β-Carbolines. [PDF]

Int J Mol Sci, 2021
Jaromin A, Gryzło B, Jamrozik M, Parapini S, Basilico N, Cegła M, Taramelli D, Zagórska A.   +7 more
europepmc   +1 more source

Deep eutectic solvent mediated synthesis of β-carbolines and related natural products via Pictet–Spengler reaction and aerobic oxidation

Tetrahedron Green Chem
An eco-friendly, one-pot synthesis of β-carboline derivatives using deep eutectic solvent is reported. This protocol utilizes commercially available aldehydes and tryptamine, involving Pictet–Spengler cyclization followed by aerobic oxidation.
Bhuvana Narasimman
doaj   +1 more source

Enantiopure Benzofuran-2-carboxamides of 1-Aryltetrahydro-β-carbolines Are Potent Antimalarials In Vitro. [PDF]

ACS Med Chem Lett, 2022
Almolhim H, Ding S, Butler JH, Bremers EK, Butschek GJ, Slebodnick C, Merino EF, Rizopoulos Z, Totrov M, Cassera MB, Carlier PR.   +10 more
europepmc   +1 more source

Syntheses of Tetrahydro-β-Carbolines via Tandem Hydformylation / Pictet-Spengler Reaction, Scope and limitations

, 2008
A novel one-pot synthesis of tetrahydro-β-carboline systems via tandem hydroformylation–Pictet–Spengler reaction starting from olefins and aryl ethylamines is described.
Bondžić, Bojan, Eilbracht, Peter
core   +1 more source

Photocatalytic enantioselective Minisci reaction of β-carbolines and application to natural product synthesis. [PDF]

Chem Sci, 2023
Luo MP, Gu YJ, Wang SG.
europepmc   +1 more source

Highly diastereoselective crystallization-induced asymmetric transformation of 1,3-disubstituted-tetrahydro-β-carbolines in water

, 2017
A green and highly stereoselective method for the synthesis of cis or trans-1,3-disubstituted-tetrahydro-β-carbolines has been developed using water as the solvent.
Xiao-Xin Shi, Zhong-Shou Huang, Hui-Ya Qu, Tian-Zhuo Meng, Yi Zhang, Qi-Qi Fan   +5 more
core   +1 more source

Preparation of 1‑Substituted Tetrahydro-β-carbolines by Lithiation–Substitution

, 2015
A method to prepare 1-substituted N-Boc-tetrahydro-β-carbolines was developed by lithiation followed by electrophilic substitution. The deprotonation to give the organolithium was optimized by in situ IR spectroscopy and showed that the Boc group rotates
Iain Coldham (1370430), Edward J. Cochrane (1370433), Lorraine A. Hassall (1370427)   +2 more
core   +1 more source

Enantioselective Catalytic Methods for the Elaboration of Chiral Tetrahydro-β-carbolines and Related Scaffolds

, 2017
Tetrahydro-β-carbolines are important synthetic intermediates in the total synthesis of natural products and of compounds exhibiting strong bioactivities.
Nicolas Glinsky-Olivier, Xavier Guinchard   +1 more
core   +1 more source

Studies into the mechanism of ifosfamide-induced encephalopathy [PDF]

, 2004
Lerch, Stefanie
core   +1 more source