(Q42147363)

English

Domino constructions of pentacyclic indeno[2,1-c]quinolines and pyrano[4,3-b]oxepines by [4+1]/[3+2+1]/[5+1] and [4+3] multiple cyclizations

scientific article published on 5 July 2012

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scholarly article

1 reference

Europe PubMed Central

17 October 2017

Domino constructions of pentacyclic indeno[2,1-c]quinolines and pyrano[4,3-b]oxepines by [4+1]/[3+2+1]/[5+1] and [4+3] multiple cyclizations (English)

1 reference

Europe PubMed Central

17 October 2017

author name string

Bo Jiang

1

1 reference

Europe PubMed Central

17 October 2017

Bao-Ming Feng

2

1 reference

Europe PubMed Central

17 October 2017

Shu-Liang Wang

3

1 reference

Europe PubMed Central

17 October 2017

Shu-Jiang Tu

4

1 reference

Europe PubMed Central

17 October 2017

Guigen Li

5

1 reference

Europe PubMed Central

17 October 2017

language of work or name

0 references

publication date

5 July 2012

1 reference

Europe PubMed Central

17 October 2017

Chemistry—A European Journal

1 reference

Europe PubMed Central

17 October 2017

18

1 reference

Europe PubMed Central

17 October 2017

32

1 reference

Europe PubMed Central

17 October 2017

9823-9826

1 reference

Europe PubMed Central

17 October 2017

A multi-component domino reaction for the direct access to polyfunctionalized indoles via intermolecular allylic esterification and indolation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

A bioinspired Ugi/Michael/aza-Michael cascade reaction in aqueous media: natural-product-like molecular diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Multicomponent reaction design in the quest for molecular complexity and diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Total synthesis and evaluation of a key series of C5-substituted vinblastine derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Four-component domino reaction providing an easy access to multifunctionalized tricyclo[6.2.2.0(1,6)]dodecane derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Oxa-azaspiro derivatives: a novel class of triple re-uptake inhibitors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Domino reactions of rhodium(II) carbenoids for alkaloid synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Total synthesis of the lycopodium alkaloid (+)-serratezomine A.

1 reference

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29 May 2018

Strategies for innovation in multicomponent reaction design

1 reference

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29 May 2018

Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

The Domino Way to Heterocycles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Enantioselective organo-cascade catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Reactions of orthophthalaldehyde with nucleophiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

On inventing reactions for atom economy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Target-oriented and diversity-oriented organic synthesis in drug discovery

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

The atom economy--a search for synthetic efficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

29 May 2018

Microwave enabled umpulong mechanism based rapid and efficient four- and six-component domino formations of 2-(2'-azaaryl)imidazoles and anti-1,2-diarylethylbenzamides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Four-component domino reaction leading to multifunctionalized quinazolines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

The domino multicomponent allylation reaction for the stereoselective synthesis of homoallylic alcohols

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Total synthesis of diverse carbogenic complexity within the resveratrol class from a common building block.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Organocatalytic asymmetric alpha-aminoxylation/aza-Michael reactions for the synthesis of functionalized tetrahydro-1,2-oxazines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

An expeditious one-step entry to the tetracyclic core of integrastatins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Heterocycles as key substrates in multicomponent reactions: the fast lane towards molecular complexity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Total synthesis of polyoxygenated cembrenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Multicomponent domino reaction from beta-ketoamides: highly efficient access to original polyfunctionalized 2,6-diazabicyclo[2.2.2]octane cores

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Multicomponent cycloadditions: the four-component [5+1+2+1] cycloaddition of vinylcyclopropanes, alkynes, and CO.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3543830

17 August 2018

Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201201109

21 January 2018

Serratezomines A--C, new alkaloids from Lycopodium serratum var. serratum

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Domino Reactions in Organic Synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A biomimetic transformation of serratinine into serratezomine A through a modified Polonovski reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of 4,5-benzotropones by cyclization of 1,3-bis-silyl enol ethers with 1,2-dialdehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biomimetic one-step access to nitraramine from simple C5 units. Revision of the previously reported structure of epinitraramine to nitraramine

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric reductive Michael cyclization

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Application of the intramolecular isomerisation-aldolisation from allylic alcohols and allylic silyl ethers to the synthesis of indanones and indenones

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereoselective RhI-catalyzed tandem conjugate addition of boronic acids-Michael cyclization

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1-Azadienes in cycloaddition and multicomponent reactions towards N-heterocycles

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facile Sc(OTf)3-catalyzed generation and successive aromatization of isobenzofuran from o-dicarbonylbenzenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Novel Electrophilic Diamination Reaction of Alkenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22767331

12 December 2020

based on heuristic

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Identifiers

10.1002/CHEM.201201109

1 reference

Europe PubMed Central

17 October 2017

1 reference

Europe PubMed Central

17 October 2017

1 reference

Europe PubMed Central

17 October 2017

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