Reaction combination opens up 3D molecular diversity for drug discovery

scientific article published in Nature

Reaction combination opens up 3D molecular diversity for drug discovery is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1106021920
P356DOI10.1038/D41586-018-05874-8
P698PubMed publication ID30097658

P2093author name stringAng Li
Wenbo Ye
P2860cites workA general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagentsQ28834226
Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters.Q34511919
Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?Q35842174
The Diels--Alder reaction in total synthesis.Q37596336
Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.Q41828474
Decarboxylative alkenylation.Q42336176
Decarboxylative Alkynylation.Q48245463
The Ireland-Claisen rearrangement strategy towards the synthesis of the schizophrenia drug, (+)-asenapine.Q50903078
Building C(sp)-rich complexity by combining cycloaddition and C-C cross-coupling reactionsQ59064328
P433issue7718
P407language of work or nameEnglishQ1860
P921main subjectdrug discoveryQ1418791
open-source drug discoveryQ75769121
molecular diversityQ129259387
P304page(s)314-316
P577publication date2018-08-01
P1433published inNatureQ180445
P1476titleReaction combination opens up 3D molecular diversity for drug discovery
P478volume560

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