scholarly article | Q13442814 |
P356 | DOI | 10.1039/C6OB00165C |
P8608 | Fatcat ID | release_gfphqctvrzgt5mnkqfcdiyfhfe |
P698 | PubMed publication ID | 26932788 |
P50 | author | Andrew Sutherland | Q43080825 |
P2093 | author name string | Claire Wilson | |
Mohamed A B Mostafa | |||
Mark W Grafton | |||
P2860 | cites work | A short history of SHELX | Q25938995 |
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Enyne metathesis (enyne bond reorganization) | Q28249083 | ||
L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor | Q28369664 | ||
Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands | Q30596579 | ||
Route to three-dimensional fragments using diversity-oriented synthesis | Q33868796 | ||
Towards the systematic exploration of chemical space | Q34039203 | ||
1,7-octadiene-assisted tandem multicomponent cross-enyne metathesis (CEYM)-Diels-Alder reactions: a useful alternative to Mori's conditions | Q34291678 | ||
Synthesis of amino-substituted indanes and tetralins via consecutive multibond-forming tandem processes | Q34777176 | ||
Ring closing enyne metathesis: a powerful tool for the synthesis of heterocycles | Q36685906 | ||
The impact of aromatic ring count on compound developability: further insights by examining carbo- and hetero-aromatic and -aliphatic ring types | Q37815587 | ||
A facile 'click' approach to novel 15β-triazolyl-5α-androstane derivatives, and an evaluation of their antiproliferative activities in vitro. | Q39406304 | ||
Netamines H-N, tricyclic alkaloids from the marine sponge Biemna laboutei and their antimalarial activity | Q41388153 | ||
Differential reactivities of enyne substrates in ruthenium- and palladium-catalyzed cycloisomerizations | Q41953948 | ||
Asymmetric Pd-Catalyzed Alkene Carboamination Reactions for the Synthesis of 2-Aminoindane Derivatives | Q42430306 | ||
Design, synthesis, and monoamine transporter binding site affinities of methoxy derivatives of indatraline | Q43512922 | ||
Synthesis of isoindolo[2,1-alpha]indoles by the palladium-catalyzed annulation of internal acetylenes | Q43655981 | ||
Synthesis and pharmacological evaluation of 3-(3,4-dichlorophenyl)-1-indanamine derivatives as nonselective ligands for biogenic amine transporters | Q44871680 | ||
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Discovery, synthetic methodology, and biological evaluation for antiphotoaging activity of bicyclic[1,2,3]triazoles: in vitro and in vivo studies. | Q50911162 | ||
Identification and synthesis of macrolide pheromones of the grain beetle Oryzaephilus surinamensis and the frog Spinomantis aglavei. | Q51161156 | ||
OLEX2: a complete structure solution, refinement and analysis program | Q56812809 | ||
Changing and challenging times for service crystallography | Q57375123 | ||
ASYMMETRIC REARRANGEMENT OF ALLYLIC TRICHLOROACETIMIDATES: PREPARATION OF (S)-2,2,2-TRICHLORO-N-(1-PROPYLALLYL)ACETAMIDE | Q57636378 | ||
Discovery of a multi-bond forming, four-step tandem process: construction of drug-like polycyclic scaffolds | Q57971593 | ||
Netamines A–G: seven new tricyclic guanidine alkaloids from the marine sponge Biemna laboutei | Q58854328 | ||
Diastereoselective synthesis of highly substituted polycyclic scaffolds via a one-pot four-step tandem catalytic process | Q58856798 | ||
A three-step tandem process for the synthesis of bicyclic γ-lactams | Q58856859 | ||
P433 | issue | 12 | |
P921 | main subject | diastereoselectivity | Q64131393 |
P304 | page(s) | 3284-3297 | |
P577 | publication date | 2016-03-02 | |
P1433 | published in | Organic and Biomolecular Chemistry | Q3355939 |
P1476 | title | A one-pot, three-step process for the diastereoselective synthesis of aminobicyclo[4.3.0]nonanes using consecutive palladium(II)- and ruthenium(II)-catalysis | |
P478 | volume | 14 |
Q57717105 | Highly Enantioselective One-Pot Synthesis of Chiral β-Heterosubstituted Alcohols via Ruthenium–Prolinamide-Catalyzed Asymmetric Transfer Hydrogenation |
Q48110758 | Structural diversification of the aminobicyclo[4.3.0]nonane skeleton using alkynylsilyl-derived allylic trichloroacetimidates |
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