Novel photochemical reactions of carbocyclic diazodiketones without elimination of nitrogen - a suitable way to N-hydrazonation of C-H-bonds

about

Novel photochemical reactions of carbocyclic diazodiketones without elimination of nitrogen - a suitable way to N-hydrazonation of C-H-bonds

Item

http://www.wikidata.org/entity/Q58697923

description

im Januar 2018 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published on 28 August 2018

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована у 2018

@uk

name

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@en

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@nl

type

Item

label

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@en

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@nl

prefLabel

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@en

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@nl

P1476

Novel photochemical reactions ...... o N-hydrazonation of C-H-bonds

@en

P2093

Dmitrij V Semenok

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

P2860

A short history of SHELX

Batch and flow photochemical benzannulations based on the reaction of ynamides and diazo ketones. Application to the synthesis of polycyclic aromatic and heteroaromatic compounds.

Modern Organic Synthesis with α-Diazocarbonyl Compounds.

SHELXT - integrated space-group and crystal-structure determination.

Concerted Wolff rearrangement in two simple acyclic diazocarbonyl compounds.

Wavelength-dependent photochemistry of Diazo Meldrum's acid and its spirocyclic isomer, Diazirino Meldrum's acid: Wolff rearrangement versus isomerization.

Experimental and theoretical investigation of reversible interconversion, thermal reactions, and wavelength-dependent photochemistry of diazo Meldrum's acid and its diazirine isomer, 6,6-dimethyl-5,7-dioxa-1,2-diaza-spiro[2,5]oct-1-ene-4,8-dione.

Experimental and theoretical analysis of the photochemistry and thermal reactivity of ethyl diazomalonate and its diazirino isomer. The role of molecular geometry in the decomposition of diazocarbonyl compounds.

Femtosecond midinfrared study of the photoinduced Wolff rearrangement of diazonaphthoquinone.

C-H carbene insertion of alpha-diazo acetamides by photolysis in non-conventional media.

P304

2250-2258

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

P31

scholarly article

P356

10.3762/BJOC.14.200

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

P407

English

P478

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

P50

P577

2018-08-28T00:00:00Z

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

P698

30202479

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

P932

6122312

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