Unified synthesis of C19-C26 subunits of amphidinolides B1, B2, and B3 by exploiting unexpected stereochemical differences in Crimmins' and Evans' aldol reactions. (Q36725473)

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scientific article published on April 2004

Language	Label	Description	Also known as
English	Unified synthesis of C19-C26 subunits of amphidinolides B1, B2, and B3 by exploiting unexpected stereochemical differences in Crimmins' and Evans' aldol reactions.	scientific article published on April 2004

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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:15049660%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Unified synthesis of C19-C26 subunits of amphidinolides B1, B2, and B3 by exploiting unexpected stereochemical differences in Crimmins' and Evans' aldol reactions (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15049660%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

2

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26 December 2019

author name string

Wei Zhang

1

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26 December 2019

Alexandre F T Yokochi

3

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26 December 2019

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publication date

1 April 2004

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26 December 2019

Journal of Organic Chemistry

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26 December 2019

69

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26 December 2019

7

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26 December 2019

2569-2572

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26 December 2019

Magnesium halide-catalyzed anti-aldol reactions of chiral N-acylthiazolidinethiones

1 reference

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30 September 2017

Total synthesis of epothilone B, epothilone D, and cis- and trans-9,10-dehydroepothilone D.

1 reference

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30 September 2017

Double diastereoselection in aldol reactions mediated by dicyclohexylchloroborane between L-erythrulose derivatives and chiral aldehydes. The Felkin-Anh versus Cornforth dichotomy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430272

5 September 2018

Ruthenium-catalyzed alkene-alkyne coupling: synthesis of the proposed structure of amphidinolide A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430272

5 September 2018

Total synthesis of (+)-amphidinolide K.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430272

5 September 2018

Asymmetric aldol additions: use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2430272

5 September 2018

Total synthesis of proposed amphidinolide A via a highly selective ring-closing metathesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective total synthesis of (+)-amphidinolide t1

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of amphidinolide T4

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Resurrecting the Cornforth Model for Carbonyl Addition: Studies on the Origin of 1,2‐Asymmetric Induction in Enolate Additions to Heteroatom‐Substituted Aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An efficient, general asymmetric synthesis of carbocyclic nucleosides: application of an asymmetric aldol/ring-closing metathesis strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An aldol approach to the synthesis of the EF fragment of spongistatin 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of the presumed amphidinolide A

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anti-selective aldol reactions with titanium enolates of N-glycolyloxazolidinethiones

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of (+)-amphidinolide P. [corrected]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Practical and highly selective oxazolidinethione-based asymmetric acetate aldol reactions with aliphatic aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

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Cytotoxic macrolides from a cultured marine dinoflagellate of the genus Amphidinium

1 reference

https://pubmed.ncbi.nlm.nih.gov/15049660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JO035829L

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15049660%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15049660%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15049660%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

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