Symmetric macrocycles by a Prins dimerization and macrocyclization strategy. (Q34001566)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19873984%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

title

Symmetric macrocycles by a Prins dimerization and macrocyclization strategy (English)

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11 February 2020

3

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11 February 2020

author name string

Michael R Gesinski

series ordinal

1

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11 February 2020

Kwanruthai Tadpetch

series ordinal

2

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11 February 2020

language of work or name

English

0 references

publication date

1 November 2009

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11 February 2020

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11 February 2020

volume

11

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11 February 2020

issue

22

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11 February 2020

page(s)

5342-5345

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Rhenium(VII) catalysis of Prins cyclization reactions

11 February 2020

cites work

1 reference

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Formal synthesis of (-)-kendomycin featuring a Prins-cyclization to construct the macrocycle

5 July 2018

1 reference

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Assignment of absolute configuration to SCH 351448 via total synthesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Efficient synthetic access to a new family of highly potent bryostatin analogues via a Prins-driven macrocyclization strategy

5 July 2018

1 reference

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Reaction of the acetals with TESOTf-base combination; speculation of the intermediates and efficient mixed acetal formation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Total synthesis of oxacyclic macrodiolide natural products

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Stereochemical diversity through cyclodimerization: synthesis of polyketide-like macrodiolides

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Total synthesis of cryptophycin-24 (Arenastatin A) amenable to structural modifications in the C16 side chain

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Total synthesis and structural revision of the marine macrolide neopeltolide

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Total synthesis of the marine natural product (-)-clavosolide A.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Total synthesis of the marine natural product (-)-clavosolide A. A showcase for the Petasis-Ferrier union/rearrangement tactic.

29 October 2018

1 reference

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Total synthesis of a diastereomer of the marine natural product clavosolide A.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Strategic use of pinacol-terminated Prins cyclizations in target-oriented total synthesis.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

New dimeric macrolide glycosides from the marine sponge Myriastra clavosa.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Total synthesis of the antiviral glycolipid cycloviracin B.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Clavosolides A and B, dimeric macrolides from the Philippines sponge Myriastra clavosa

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2905591

Highly enantioselective Alk-2-enylation of aldehydes through an allyl-transfer reaction

29 October 2018

1 reference

12 December 2020

Total synthesis of (-)-cylindrocyclophanes A and F exploiting the reversible nature of the olefin cross metathesis reaction

1 reference

12 December 2020

The first and highly enantioselective crotylation of aldehydes via an allyl-transfer reaction from a chiral crotyl-donor

1 reference

12 December 2020

Stereoselective synthesis of 4-hydroxy-2,3,6-trisubstituted tetrahydropyrans

1 reference

12 December 2020

Sequential acyl halide-aldehyde cyclocondensation and enzymatic resolution as a route to enantiomerically enriched beta-lactones

1 reference

12 December 2020

Total synthesis, structural revision, and absolute configuration of (-)-clavosolide [corrected] A

1 reference

12 December 2020

Total synthesis of (+)-neopeltolide by a Prins macrocyclization

1 reference

12 December 2020

Total synthesis of efomycine M

1 reference

12 December 2020

An efficient formal synthesis of (-)-clavosolide a featuring a "mismatched" stereoselective oxocarbenium reduction

1 reference

12 December 2020

Total synthesis of marinomycins A-C

1 reference

12 December 2020

Identifiers

DOI

10.1021/OL9022062

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19873984%20AND%20SRC:MED&resulttype=core&format=json

release_7dql5nbgdbh3dkduxhckq6fpei

11 February 2020

Fatcat ID

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Fatcat

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24 November 2022

mapped directly with Wikidata item

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19873984%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

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