Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles

about

Organocatalytic Asymmetric Synthesis of Spiro-Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One-Pot Michael-Henry-Cascade-Rearrangement Reactions.

P2860

Q48303054-BDED9F45-76A0-4345-8823-E5D633F25EB9

P2860

Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles

Item

http://www.wikidata.org/entity/Q57844088

description

im April 2017 veröffentlichter wissenschaftlicher Artikel

@de

wetenschappelijk artikel

@nl

наукова стаття, опублікована у квітні 2017

@uk

name

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@en

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@nl

type

Item

label

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@en

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@nl

prefLabel

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@en

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@nl

P1476

Formal (4+1) Cycloaddition and ...... s and Spirooxindole Polycycles

@en

P2093

Kenji Monde

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

Muhammad Sohail

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

Tohru Taniguchi

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

P2860

Total synthesis of Elisabethin A: intramolecular Diels-Alder reaction under biomimetic conditions.

An oxidative dearomatization-induced [5 + 2] cascade enabling the syntheses of α-cedrene, α-pipitzol, and sec-cedrenol.

Dysiherbols A-C and Dysideanone E, Cytotoxic and NF-κB Inhibitory Tetracyclic Meroterpenes from a Dysidea sp. Marine Sponge.

Quinidine thiourea-catalyzed aldol reaction of unactivated ketones: highly enantioselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones.

Highly diastereo- and enantioselective organocatalytic michael addition of α-ketoamides to nitroalkenes.

Asymmetric quadruple aminocatalytic domino reactions to fused carbocycles incorporating a spirooxindole motif.

A phosphine-catalyzed [3+2] cycloaddition strategy leading to the first total synthesis of (-)-hinesol.

A general strategy to elisabethane diterpenes: stereocontrolled synthesis of elisapterosin B via oxidative cyclization of an elisabethin precursor.

Efficient total syntheses of (-)-colombiasin A and (-)-elisapterosin B: application of the Cr-catalyzed asymmetric quinone Diels-Alder reaction.

Combined C-H activation/cope rearrangement as a strategic reaction in organic synthesis: total synthesis of (-)-colombiasin a and (-)-elisapterosin B.

P304

5947-5951

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

P31

scholarly article

P356

10.1002/ANGE.201701049

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

P433

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

P478

129

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

P50

Fujie Tanaka

Ji-Rong Huang

P577

2017-04-11T00:00:00Z

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

P921

enantioselectivity

cycloaddition

Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles

about

P2860

P2860

Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P921