Phosphoramidate tantalum complexes for room-temperature C-H functionalization: hydroaminoalkylation catalysis. - Wikidata - awgldk - TriplyDB

Phosphoramidate tantalum complexes for room-temperature C-H functionalization: hydroaminoalkylation catalysis.

Phosphoramidate tantalum complexes for room-temperature C-H functionalization: hydroaminoalkylation catalysis.

http://www.wikidata.org/entity/Q45777833

about

Recent advances in catalytic C-N bond formation: a comparison of cascade hydroaminomethylation and reductive amination reactions with the corresponding hydroamidomethylation and reductive amidation reactions.Methyl Complexes of the Transition Metals.α-Arylation of Saturated Azacycles and N-Methylamines via Palladium(II)-Catalyzed C(sp(3))-H Coupling.Scandium-catalysed intermolecular hydroaminoalkylation of olefins with aliphatic tertiary amines Probing Phosphorus Nitride (P≡N) and Other Elusive Species Formed upon Pyrolysis of Dimethyl Phosphoramidate.Synthesis and reactivity of Li and TaMe3 complexes supported by N,N'-bis(2,6-diisopropylphenyl)-o-phenylenediamido ligands.Practical Alkoxythiocarbonyl Auxiliaries for Iridium(I)-Catalyzed C-H Alkylation of Azacycles.Intermolecular hydroaminoalkylation of alkenes and dienes using a titanium mono(formamidinate) catalyst.One-Pot Procedure for the Synthesis of 1,5-Benzodiazepines from N-Allyl-2-bromoanilines.Hydroaminoalkylation of Allylsilanes and a One-Pot Procedure for the Synthesis of 1,5-Benzoazasilepines.

P2860

Q38237439-46F80CD2-8023-4F98-B28C-609DF3A52AF4 Q38780168-C93AA943-A233-4F35-AA92-F10BCA4B0EF3 Q39914728-6549BFCF-9561-4D04-9301-482948686545 Q42315603-256CD8D0-B07C-40A5-9086-181E8EB4B83E Q46389906-0ECD838D-3333-4D9F-8A08-5D0CDA849285 Q46536391-24B81AA0-EF8D-4076-9764-4F8ACE893930 Q48268047-154E50D2-CAD8-4ADF-8977-EA8C32EE9891 Q53609719-16509451-40E1-40EA-8753-21727CD9F1CD Q53666091-F1C1E735-4413-4CEA-96FC-4AB9B1495489 Q54173360-29EA2262-DA20-467B-A959-FC1457515FB3

P2860

Phosphoramidate tantalum complexes for room-temperature C-H functionalization: hydroaminoalkylation catalysis.

http://www.wikidata.org/entity/Q45777833

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh-hant

name

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@en

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@nl

type

label

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@en

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@nl

prefLabel

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@en

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@nl

P1433

Q45777833-06287D0D-8FF7-4525-8493-8B869A7AB78B

P1476

Q45777833-D2F26289-484B-44EA-BCDD-C20D05CD23DC

P2093

Q45777833-49373E22-41EC-4B79-AD15-B6035554FCE1

Q45777833-93611A1E-ABC7-4E04-A1AC-F3492B29BA9C

Q45777833-C2BB24EF-47B9-470C-98C3-02408D165B9F

Q45777833-C6D58A6E-1613-45AE-B707-2BB9CC56422E

P2860

Q45777833-05754D48-354C-40A1-84D9-F06405343A88

Q45777833-1761B63F-3A88-4EF0-8104-089B5B13CB3F

Q45777833-4079BC61-8F15-4B6D-A582-2B903140F4B3

Q45777833-61BD35A8-6CD2-4A12-A0FC-90511AED0C43

Q45777833-80D607D6-CC74-4FFF-AB5C-A2E0397B8EA5

Q45777833-A69950CF-8C64-46A8-9460-B5A722A27FD6

Q45777833-AB1AD85F-BBFC-4EFC-A82B-6AA6CBEB00B9

Q45777833-B8A1D468-13F9-41F8-8605-9CA09B2B8FFA

Q45777833-C5642521-7E99-41B1-AB05-859686098AC7

Q45777833-D0FA12CC-06B8-4569-810C-653D5CB86CD4

P304

Q45777833-19C0FC3F-B9AA-4D6A-BE18-2C173C14996C

P31

Q45777833-B1178F0D-805D-47AE-8FA8-711A95C5A0E7

P356

Q45777833-B21579A9-AEFE-4C6F-96DC-69E00C0750A4

P407

Q45777833-893EFDF5-686E-412B-A658-15D866547F5F

P433

Q45777833-C25E225F-DB2A-41C5-BC81-99B001CB568B

P478

Q45777833-0CC2F4F8-2D96-4393-B2A4-BE5D295FA175

P577

Q45777833-F582A11D-86F1-4AB8-A2F9-1456D4A5FD04

P698

Q45777833-21788A54-0C4E-41BA-BC7E-944E52203054

P356

P1433

Angewandte Chemie International Edition

P1476

Phosphoramidate tantalum compl ...... ydroaminoalkylation catalysis.

@en

P2093

Laurel L Schafer

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

Mitchell R Perry

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

Pierre Garcia

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

Ying Yin Lau

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

P2860

Green chemistry: principles and practice.

Direct, catalytic hydroaminoalkylation of unactivated olefins with N-alkyl arylamines

Hydroaminoalkylation of unactivated olefins with dialkylamines.

Photoredox functionalization of C-H bonds adjacent to a nitrogen atom.

Ru(3)(CO)(12)-catalyzed coupling reaction of sp(3) C-H bonds adjacent to a nitrogen atom in alkylamines with alkenes.

Titanium-catalyzed intermolecular hydroaminoalkylation of conjugated dienes.

TaMe3Cl2-catalyzed intermolecular hydroaminoalkylation: a simple complex for enhanced reactivity and expanded substrate scope.

Chemoselective Staudinger-phosphite reaction of azides for the phosphorylation of proteins.

Systematic repression of beta-silyl carbocation stabilization.

Selective C-H activation alpha to primary amines. Bridging metallaaziridines for catalytic, intramolecular alpha-alkylation.

P304

9144-9148

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

P31

scholarly article

P356

10.1002/ANIE.201304153

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

P407

P433

35

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

P478

52

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

P577

2013-07-23T00:00:00Z

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

P698

23881625

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