Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles. - Wikidata - wikimedia - TriplyDB

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

http://www.wikidata.org/entity/Q33998747

about

Inhibition of myeloperoxidase: evaluation of 2H-indazoles and 1H-indazolones.Diverting Reactive Intermediates Toward Unusual Chemistry: Unexpected Anthranil Products from Davis-Beirut Reaction.

P2860

Q27325561-D3F2399B-510A-4490-8DB4-54B20ED8E31E Q46093306-82249BED-CD66-4CE9-89FA-9373B496BA0B

P2860

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

http://www.wikidata.org/entity/Q33998747

description

2014 nî lūn-bûn

@nan

2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@ast

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@en

type

label

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@ast

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@en

prefLabel

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@ast

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@en

P1433

Q33998747-57592860-41D1-4134-92F7-F2A9A220C595

P1476

Q33998747-7D7A4BA3-C6C1-4EF6-882D-97599B624498

P2093

Q33998747-021F9490-9B35-4C21-A194-1B5A72C0A3EB

Q33998747-2D3D0EEB-166F-4D10-9C7D-A99F592DE2CD

Q33998747-F55D26BC-993D-43E2-8B9D-F05196BF66B9

P2860

Q33998747-0C1624B5-EB72-4DE4-B321-1765293164F3

Q33998747-22D7D706-846C-4CCB-8E56-5D1FACA4337C

Q33998747-23356FC4-D4D6-4B08-943E-EEBFFC555DF5

Q33998747-264A8DCF-5F37-4D0A-9C49-150545FF1CC1

Q33998747-4598CD2A-B652-4E87-82C6-A0F22032D3C9

Q33998747-62038192-B458-41EE-9BFE-1ED6BC94B5BD

Q33998747-723DBDD0-F851-4A8D-AEB0-C50D8E53343A

Q33998747-7EBDD8D2-7855-4509-AB87-5A23A03197BD

Q33998747-89DEA81F-D041-4540-B45B-BBF4C9FDFB19

Q33998747-8C9F6171-8A30-4927-98DC-AC960F3B605E

P304

Q33998747-AEDEE89D-D33E-4D86-A158-4AD9529DA288

P31

Q33998747-104A5A0C-A709-4CBE-A6DB-0357C12CE78B

P356

Q33998747-B1B5D711-6691-4241-9BED-CE316CD75D69

P407

Q33998747-109EB383-098E-4D9C-A2E5-F85DEE780C97

P433

Q33998747-BEA0AA83-516D-4D4F-8964-F193784512F9

P478

Q33998747-106AABD2-F49E-4503-8B62-B9BA0CD65B7C

P577

Q33998747-572B8842-160F-441E-B3EF-0059F4AE5518

P5875

Q33998747-0DFA40F0-5A17-44C3-A0F8-0148B00F438E

P698

Q33998747-A098AD5B-A595-4B7E-89D6-07BEB6F1CE17

P932

Q33998747-024E303E-876F-4E70-904B-12D0A7064512

P356

P1433

Journal of Organic Chemistry

P1476

Davis-Beirut reaction: route to thiazolo-, thiazino-, and thiazepino-2H-indazoles.

@en

P2093

Kelli M Farber

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

Makhluf J Haddadin

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

Mark J Kurth

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

P2860

The Davis-Beirut reaction: N1,N2-disubstituted-1H-indazolones via 1,6-electrophilic addition to 3-alkoxy-2H-indazoles

Synthesis of a library of 2-alkyl-3-alkyloxy-2H-indazole-6-carboxamides.

Claimed 2,1-benzisoxazoles are indazalones.

N,N-bond-forming heterocyclization: synthesis of 3-alkoxy-2H-indazoles.

Nucleophilic substitution of oxazino-/oxazolino-/benzoxazin [3,2-b]indazoles: an effective route to 1H-indazolones.

Facile syntheses of novel benzo-1,3-dioxolo-, benzothiazolo-, pyrido-, and quinolino-fused 5H-benzo[d]-pyrazolo[5,1-b][1,3]-oxazines and 1H-pyrazoles.

Structure-activity relationships of cyanoquinolines with corrector-potentiator activity in ΔF508 cystic fibrosis transmembrane conductance regulator protein

Biogenesis of iron-sulfur clusters in mammalian cells: new insights and relevance to human disease.

Neutrophil recruitment and airway epithelial cell involvement in chronic cystic fibrosis lung disease.

A one-pot-three-step route to triazolotriazepinoindazolones from oxazolino-2H-indazoles

P304

6939-6945

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

P31

scholarly article

P356

10.1021/JO501014E

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

P407

P433

15

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

P478

79

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

P577

2014-07-23T00:00:00Z

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

P5875

263899350

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

P698

25019525

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

P932

4120971

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