Arthur C. Cope Scholar Awards and Eli Lilly Award - Wikidata - wikimedia - TriplyDB

Arthur C. Cope Scholar Awards and Eli Lilly Award

Arthur C. Cope Scholar Awards and Eli Lilly Award

http://www.wikidata.org/entity/Q57657251

about

Arthur C. Cope Scholar Awards and Eli Lilly Award

http://www.wikidata.org/entity/Q57657251

description

wetenschappelijk artikel

@nl

наукова стаття, опублікована в липні 2012

@uk

name

Arthur C. Cope Scholar Awards and Eli Lilly Award

@en

Arthur C. Cope Scholar Awards and Eli Lilly Award

@nl

type

label

Arthur C. Cope Scholar Awards and Eli Lilly Award

@en

Arthur C. Cope Scholar Awards and Eli Lilly Award

@nl

prefLabel

Arthur C. Cope Scholar Awards and Eli Lilly Award

@en

Arthur C. Cope Scholar Awards and Eli Lilly Award

@nl

P1433

Q57657251-9B47EAA2-9677-4C99-8B6B-E28AF0D2D292

P1476

Q57657251-1B7FF40D-1753-4D2A-A7B6-E746FDBD36D1

P2860

Q57657251-08AA89C9-BBF5-485A-B890-CB2B38BAD37A

Q57657251-36508E73-B277-4082-BBD7-5C794D5846A4

Q57657251-689D4CDF-220B-474D-9860-2AFAC65252D4

Q57657251-8B6AABE5-E250-4333-A909-961300C7D9BC

Q57657251-A2EDB5D4-1E65-4263-9681-22A250CAE72A

Q57657251-D4810A05-D1AF-48E2-B6BB-B54CA009DF84

Q57657251-E5528F1F-E561-47F0-AB6B-781614A77422

Q57657251-EB7DD3BA-A1B8-4ACD-A1F0-8BAFD53BF810

P304

Q57657251-A80B8230-9C64-4856-87DB-296751DAB4E9

P31

Q57657251-3D047BE5-FD58-4E8E-96C9-2772700F2B71

P356

Q57657251-D04BF07C-B735-40CA-8C1C-058C536C7333

P407

Q57657251-32DEEC10-B47C-4598-9D53-72B46FD7AE45

P433

Q57657251-322893A6-4EB6-4F83-8FB1-E002785ECA6B

P478

Q57657251-BE4A56D6-6003-449F-9EF4-F0A4C87B4949

P577

Q57657251-1EACBF52-2DE5-416B-A43B-063E71BF9A89

P356

P1433

Angewandte Chemie International Edition

P1476

Arthur C. Cope Scholar Awards and Eli Lilly Award

@en

P2860

1,3-allylic strain as a strategic diversification element for constructing libraries of substituted 2-arylpiperidines.

Total syntheses of hopeanol and hopeahainol A empowered by a chiral Brønsted acid induced pinacol rearrangement.

Epoxide-opening cascades in the synthesis of polycyclic polyether natural products.

A bright and specific fluorescent sensor for mercury in water, cells, and tissue.

Comparing spin-selective charge transport through donor-bridge-acceptor molecules with different oligomeric aromatic bridges.

Identification of OxyE as an ancillary oxygenase during tetracycline biosynthesis.

Investigation of tailoring modifications in pradimicin biosynthesis.

Synthesis, Characterization, and Photoinduced Energy and Electron Transfer in a Supramolecular Tetrakis (Ruthenium(II) Phthalocyanine) Perylenediimide Pentad

P304

8693-8694

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/ANIE.201204828

http://www.w3.org/2001/XMLSchema#string

P407

P433

35

http://www.w3.org/2001/XMLSchema#string

P478

51

http://www.w3.org/2001/XMLSchema#string

P577

2012-07-13T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime