(Q83174860)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21226170%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Disulfonimide-catalyzed asymmetric vinylogous and bisvinylogous Mukaiyama aldol reactions (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21226170%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

5

Benjamin List

1 reference

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19 January 2020

author name string

Lars Ratjen

1

1 reference

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19 January 2020

Pilar García-García

2

1 reference

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19 January 2020

Frank Lay

3

1 reference

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19 January 2020

Michael Edmund Beck

4

1 reference

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19 January 2020

publication date

17 December 2010

1 reference

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Angewandte Chemie International Edition

19 January 2020

published in

1 reference

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19 January 2020

volume

50

1 reference

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19 January 2020

issue

3

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19 January 2020

page(s)

754-758

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21226170%20AND%20SRC:MED&resulttype=core&format=json

Do Fukui function maxima relate to sites of metabolism? A critical case study

19 January 2020

cites work

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

BINBAM - A New Motif for Strong and Chiral Brønsted Acids

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Hydrogen bond catalyzed enantioselective vinylogous Mukaiyama aldol reaction

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Lewis base activation of Lewis acids: catalytic, enantioselective addition of silyl ketene acetals to aldehydes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Lewis base activation of lewis acids. Addition of silyl ketene acetals to aldehydes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

A Powerful Chiral Counteranion Motif for Asymmetric Catalysis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Enantioselective synthesis and structure revision of solandelactone E.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

A catalytic asymmetric vinylogous Mukaiyama aldol reaction

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

The aldol addition reaction: an old transformation at constant rebirth

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Asymmetric total synthesis of solandelactone E: stereocontrolled synthesis of the 2-ene-1,4-diol core through a lithiation-borylation-allylation sequence

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Rapid access to polyketide scaffolds via vinylogous Mukaiyama aldol reactions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Mixed Crossed Aldol Condensation between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6-diphenylphenoxide)

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Catalytic Asymmetric Vinylogous Mukaiyama-aldol (CAVM) reactions: the enolate activation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Apparent Catalytic Generation of Chiral Metal Enolates: Enantioselective Dienolate Additions to Aldehydes Mediated by Tol-BINAP·Cu(II) Fluoride Complexes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Stereocontrolled total synthesis of (-)-callipeltoside A

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Solandelactones A-I, lactonized cyclopropyl oxylipins isolated from the hydroid Solanderia secunda

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Total synthesis of RK-397

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Oxazaborolidinone-promoted vinylogous Mukaiyama aldol reactions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Modern aldol methods for the total synthesis of polyketides

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Catalytic, enantioselective, vinylogous aldol reactions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Lasonolide A: structural revision and synthesis of the unnatural (-)-enantiomer

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Studies on the synthesis of furanosteroids. I. Viridin models

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Total Synthesis of Macrolactin A with Versatile Catalytic, Enantioselective Dienolate Aldol Addition Reactions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

NEW ALDOL TYPE REACTION

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Lewis base activation of Lewis acids. Vinylogous aldol reactions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Total Synthesis of (+)-Ratjadone

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Total Synthesis of (+)-Papulacandin D

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Total synthesis of (+)-lasonolide A

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.201005954

Identifiers

DOI

10.1002/ANIE.201005954

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21226170%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference