(Q46254500)

English

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

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

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

enantioselectivity

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based on heuristic

inferred from title

Marisa C. Kozlowski

2

object named as

Marisa C Kozlowski

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

author name string

Elizabeth C Linton

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

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publication date

1 December 2008

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

Journal of the American Chemical Society

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

130

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

48

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

16162-16163

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine-Derived Fungus,Aspergillus sp

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9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/ANIE.200604381

Identifiers

10.1021/JA807026Z

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/18998679

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