(Q73926727)

English

A mechanistically guided design leads to the synthesis of an efficient and practical new reagent for the highly enantioselective, catalytic dihydroxylation of olefins

scientific article published on 01 September 2003

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A mechanistically guided design leads to the synthesis of an efficient and practical new reagent for the highly enantioselective, catalytic dihydroxylation of olefins (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

enantioselectivity

1 reference

based on heuristic

inferred from title

Elias James Corey

2

object named as

E J Corey

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

Jinkun Huang

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 September 2003

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Organic Letters

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

5

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

19

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

3455-3458

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

The application of a mechanistic model leads to the extension of the Sharpless asymmetric dihydroxylation to allylic 4-methoxybenzoates and conformationally related amine and homoallylic alcohol derivatives

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Kinetic Investigations Provide Additional Evidence That an Enzyme-like Binding Pocket Is Crucial for High Enantioselectivity in the Bis-Cinchona Alkaloid Catalyzed Asymmetric Dihydroxylation of Olefins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Oxygen and Osmium-A New Alliance for Dihydroxylations?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Catalytic Asymmetric Dihydroxylation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Experimental test of the [3+2]- and [2+2]-cycloaddition pathways for the bis-cinchona alkaloid-OsO4 catalyzed dihydroxylation of olefins by means of kinetic isotope effects

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

X-ray crystallographic studies provide additional evidence that an enzyme-like binding pocket is crucial to the enantioselective dihydroxylation of olefins by OsO4—bis-cinchona alkaloid complexes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Rigid and highly enantioselective catalyst for the dihydroxylation of olefins using osmium tetraoxide clarifies the origin of enantiospecificity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Highly effective transition structure designed catalyst for the enantio- and position-selective dihydroxylation of polyisoprenoids

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/OL035192S

Improved enantioselective dihydroxylation of bishomoallylic alcohol derivatives using a mechanistically inspired bis-cinchona alkaloid catalyst

1 reference

19 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1016/0040-4039(96)00163-3

Identifiers

10.1021/OL035192S

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12967298%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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