Detalhe da pesquisa
1.
9-Azahomocubane.
Chemistry
; 30(3): e202303133, 2024 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37823679
2.
seco-1-Azacubane-2-carboxylic Acid: Derivative Scope and Comparative Biological Evaluation.
J Org Chem
; 89(1): 798-803, 2024 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38131648
3.
seco-1-Azacubane-2-carboxylic acid-Amide Bond Comparison to Proline.
J Org Chem
; 88(18): 12867-12871, 2023 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37647582
4.
Isolation and In Vitro and In Vivo Activity of Secondary Metabolites from Clerodendrum polycephalum Baker against Plasmodium Malaria Parasites.
J Nat Prod
; 86(12): 2661-2671, 2023 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37972998
5.
A New Metric for Evaluating DFT Calculated Proton and Carbon Chemical Shifts of Natural Products and Organic Compounds.
Chemphyschem
; 22(21): 2207-2214, 2021 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34546658
6.
Synthesis, isolation and characterisation of fluorinated-benzimidazoisoquinoline regioisomers.
Magn Reson Chem
; 59(11): 1154-1159, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34250653
7.
Synthetic Tigliane Intermediates Engage Thiols to Induce Potent Cell Line Selective Anti-Cancer Activity.
Chemistry
; 26(59): 13372-13377, 2020 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32991008
8.
Chemical constituents from Macleaya cordata (Willd) R. Br. and their phenotypic functions against a Parkinson's disease patient-derived cell line.
Bioorg Med Chem
; 28(21): 115732, 2020 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33065438
9.
Dynamic NMR and Computational Studies Inform the Conformational Description of Dendrillane Terpenes from the Nudibranch Goniobranchus coi.
J Nat Prod
; 83(3): 714-719, 2020 03 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31913035
10.
Elucidation of Relative and Absolute Configurations of Highly Rearranged Diterpenoids and Evidence for a Putative Biosynthetic Intermediate from the Australian Nudibranch Goniobranchus geometricus.
J Nat Prod
; 82(3): 449-455, 2019 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-30418031
11.
Catalyst-Controlled Stereoselective Synthesis Secures the Structure of the Antimalarial Isocyanoterpene Pustulosaisonitrile-1.
J Org Chem
; 82(24): 13313-13323, 2017 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29124922
12.
Antitubercular and Cytotoxic Chlorinated seco-Cyclohexenes from Uvaria alba.
J Nat Prod
; 80(12): 3319-3323, 2017 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29172496
13.
Revision of the Structure of Acremine P from a Marine-Derived Strain of Acremonium persicinum.
Molecules
; 22(4)2017 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28338628
14.
Rhodocomatulin-Type Anthraquinones from the Australian Marine Invertebrates Clathria hirsuta and Comatula rotalaria.
J Nat Prod
; 79(4): 946-53, 2016 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-27063022
15.
Rearranged Diterpenes and Norditerpenes from Three Australian Goniobranchus Mollusks.
J Nat Prod
; 79(3): 477-83, 2016 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26698272
16.
Investigation of two- and three-bond carbon-hydrogen coupling constants in cinnamic acid based compounds.
Magn Reson Chem
; 54(12): 941-946, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27356919
17.
Comparison of experimental and DFT-calculated NMR chemical shifts of 2-amino and 2-hydroxyl substituted phenyl benzimidazoles, benzoxazoles and benzothiazoles in four solvents using the IEF-PCM solvation model.
Magn Reson Chem
; 54(4): 298-307, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26478462
18.
Antimalarial Isocyano and Isothiocyanato Sesquiterpenes with Tri- and Bicyclic Skeletons from the Nudibranch Phyllidia ocellata.
J Nat Prod
; 78(6): 1422-7, 2015 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26056748
19.
1H and 13C NMR scaling factors for the calculation of chemical shifts in commonly used solvents using density functional theory.
J Comput Chem
; 35(18): 1388-94, 2014 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24854878
20.
Synthesis, NMR structural characterization and molecular modeling of substituted thiosemicarbazones and semicarbazones using DFT calculations to prove the syn/anti isomer formation.
Magn Reson Chem
; 52(3): 98-105, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24436057