One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

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Regioselective Direct C-Alkenylation of Indoles.Ligand-based Modeling for the Prediction of Pharmacophore Features for Multi-targeted Inhibition of the Arachidonic Acid Cascade.

P2860

Q39391359-B1F556C0-894D-47D9-B2EC-DB8814FF5136 Q47678019-FA8D2953-6A39-4F72-B90B-5E33C98D888C

P2860

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

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http://www.wikidata.org/entity/Q53665687

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2015 nî lūn-bûn

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2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@en

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@nl

type

Item

label

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@en

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@nl

prefLabel

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@en

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@nl

P1476

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

@en

P2093

Dongari Yadagiri

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

Shanmugam Rajasekar

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

P2860

Total synthesis of vinblastine, related natural products, and key analogues and development of inspired methodology suitable for the systematic study of their structure-function properties

2-Substituted tryptamines: agents with selectivity for 5-HT(6) serotonin receptors

Mapping the melatonin receptor. 6. Melatonin agonists and antagonists derived from 6H-isoindolo[2,1-a]indoles, 5,6-dihydroindolo[2,1-a]isoquinolines, and 6,7-dihydro-5H-benzo[c]azepino[2,1-a]indoles

Pharmacological properties of tetrahydronorharmane (tryptoline).

Rhodium-catalyzed enantioselective cyclopropanation of olefins with N-sulfonyl 1,2,3-triazoles

Catalytic asymmetric transannulation of NH-1,2,3-triazoles with olefins.

Efficient synthesis of 1-sulfonyl-1,2,3-triazoles

Chemistry and biology of monoterpene indole alkaloid biosynthesis.

The expanded biology of serotonin.

Catalytic asymmetric C-H insertions of rhodium(II) azavinyl carbenes.

P304

17079-17084

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P31

scholarly article

P356

10.1002/CHEM.201502201

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P407

English

P433

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

P478

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

P50

Pazhamalai Anbarasan

P577

2015-10-07T00:00:00Z

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P698

26443500

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One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

about

P2860

P2860

One-Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698