(Q50481464)

English

Organocatalytic Michael addition of malonates to isatylidene-3-acetaldehydes: application to the total synthesis of (-)-debromoflustramine E.

scientific article published on 23 April 2013

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

Organocatalytic Michael addition of malonates to isatylidene-3-acetaldehydes: application to the total synthesis of (-)-debromoflustramine E. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

Organocatalysis

1 reference

based on heuristic

inferred from title

author name string

Renrong Liu

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

Junliang Zhang

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

language of work or name

0 references

publication date

23 April 2013

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

Chemistry—A European Journal

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

19

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

23

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

7319-7323

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Gelsemine: a thought-provoking target for total synthesis

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Molybdenum-catalyzed asymmetric allylation of 3-alkyloxindoles: application to the formal total synthesis of (-)-physostigmine.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Mo-catalyzed regio-, diastereo-, and enantioselective allylic alkylation of 3-aryloxindoles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Palladium-catalyzed asymmetric allylation of prochiral nucleophiles: synthesis of 3-allyl-3-aryl oxindoles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Cinchona-alkaloid-catalyzed enantioselective direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Thiourea-catalyzed highly enantio- and diastereoselective additions of oxindoles to nitroolefins: application to the formal synthesis of (+)-physostigmine.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

A homodinuclear Mn(III)2-Schiff base complex for catalytic asymmetric 1,4-additions of oxindoles to nitroalkenes.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Enantioselective base-free phase-transfer reaction in water-rich solvent

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Asymmetric conjugate addition of oxindoles to 2-chloroacrylonitrile: a highly effective organocatalytic strategy for simultaneous construction of 1,3-nonadjacent stereocenters leading to chiral pyrroloindolines

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Stereocontrolled Creation of All‐Carbon Quaternary Stereocenters by Organocatalytic Conjugate Addition of Oxindoles to Vinyl Sulfone

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Chiral calcium VAPOL phosphate mediated asymmetric chlorination and Michael reactions of 3-substituted oxindoles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

The asymmetric intramolecular Heck reaction in natural product total synthesis

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

AcOLeDMAP and BnOLeDMAP: conformationally restricted nucleophilic catalysts for enantioselective rearrangement of indolyl acetates and carbonates

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Enantioselective total synthesis of (+)-gliocladin C.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Catalytic enantioselective Meerwein-Eschenmoser Claisen rearrangement: asymmetric synthesis of allyl oxindoles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Asymmetric synthesis of allenyl oxindoles and spirooxindoles by a catalytic enantioselective Saucy-Marbet Claisen rearrangement

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Catalytic enantioselective stereoablative alkylation of 3-halooxindoles: facile access to oxindoles with C3 all-carbon quaternary stereocenters

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Enantioselective construction of spirocyclic oxindolic cyclopentanes by palladium-catalyzed trimethylenemethane-[3+2]-cycloaddition

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Targeting structural and stereochemical complexity by organocascade catalysis: construction of spirocyclic oxindoles having multiple stereocenters

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Core-structure-motivated design of a phosphine-catalyzed [3+2] cycloaddition reaction: enantioselective syntheses of spirocyclopenteneoxindoles.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Highly efficient hydrogen-bonding catalysis of the Diels-Alder reaction of 3-vinylindoles and methyleneindolinones provides carbazolespirooxindole skeletons.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Organocatalytic synthesis of spiro[pyrrolidin-3,3'-oxindoles] with high enantiopurity and structural diversity.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Organocatalytic tandem reaction to construct six-membered spirocyclic oxindoles with multiple chiral centres through a formal [2+2+2] annulation

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Highly enantioselective construction of spiro[4H-pyran-3,3'-oxindoles] through a domino Knoevenagel/Michael/cyclization sequence catalyzed by cupreine

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

The diarylprolinol silyl ether system: a general organocatalyst.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Iminium catalysis

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Asymmetric organocatalytic epoxidation of alpha,beta-unsaturated aldehydes with hydrogen peroxide

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Enantioselective synthesis of polysubstituted cyclopentanones by organocatalytic double Michael addition reactions

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Water-compatible iminium activation: organocatalytic Michael reactions of carbon-centered nucleophiles with enals

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Enantioselective total synthesis of (-)-flustramines A, B and (-)-flustramides A, B via domino olefination/isomerization/Claisen rearrangement sequence

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Total synthesis of (+/-)-flustramines A and C, (+/-)-flustramide A, and (-)- and (+)-debromoflustramines A.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Antibacterial activity of (-)-deoxypseudophrynaminol versus its racemate and derivatives

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Synthesis and biological evaluation of (-)- and (+)-debromoflustramine B and its analogues as selective butyrylcholinesterase inhibitors.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Molybdenum-catalyzed asymmetric allylic alkylation of 3-alkyloxindoles: reaction development and applications

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Exercising regiocontrol in palladium-catalyzed asymmetric prenylations and geranylation: unifying strategy toward flustramines A and B.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

It all began with an error: the nomofungin/communesin story

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Cinchona alkaloid-based phosphoramide catalyzed highly enantioselective Michael addition of unprotected 3-substituted oxindoles to nitroolefins

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Asymmetric Michael Addition of N-Boc-Protected Oxindoles to Nitroalkenes Catalyzed by a Chiral Secondary Amine

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Organocatalytic Michael-alkylation cascade: the enantioselective nitrocyclopropanation of oxindoles

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201300977

21 January 2018

Identifiers

10.1002/CHEM.201300977

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23613445

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50481464&oldid=1508732132"