(Q36995709)

English

Efficient and selective syntheses of (all-E)- and (6E,10Z)-2'-O-methylmyxalamides D via Pd-catalyzed alkenylation--carbonyl olefination synergy

scientific article published on 02 July 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Efficient and selective syntheses of (all-E)- and (6E,10Z)-2'-O-methylmyxalamides D via Pd-catalyzed alkenylation--carbonyl olefination synergy (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

author name string

Guangwei Wang

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Zhihong Huang

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Ei-Ichi Negishi

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

language of work or name

0 references

publication date

2 July 2008

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Organic Letters

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

15

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

3223-3226

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Highly stereo- and regioselective synthesis of (Z)-trisubstituted alkenes via 1-bromo-1-alkyne hydroboration-migratory insertion-Zn-promoted iodinolysis and Pd-catalyzed organozinc cross-coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

29 September 2017

Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

29 September 2017

Total synthesis of 2'-O-methylmyxalamide D and (6E)-2'-O-methylmyxalamide D

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

29 September 2017

Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

29 September 2017

Efficient and selective synthesis of 6,7-Dehydrostipiamide via Zr-catalyzed asymmetric carboalumination and Pd-catalyzed cross-coupling of organozincs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

29 September 2017

Palladium-catalyzed alkynylation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

29 September 2017

1,4-Pentenyne as a five-carbon synthon for efficient and selective syntheses of natural products containing 2,4-dimethyl-1-penten-1,5-ylidene and related moieties by means of Zr-catalyzed carboalumination of alkynes and alkenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

27 June 2018

Recent advances in efficient and selective synthesis of di-, tri-, and tetrasubstituted alkenes via Pd-catalyzed alkenylation-carbonyl olefination synergy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

4 September 2018

Total synthesis of (-)-archazolid B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

4 September 2018

Catalytic, efficient, and syn-selective construction of deoxypolypropionates and other chiral compounds via Zr-catalyzed asymmetric carboalumination of allyl alcohol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

4 September 2018

An efficient and general method for the synthesis of alpha,omega-difunctional reduced polypropionates by Zr-catalyzed asymmetric carboalumination: synthesis of the scyphostatin side chain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2593746

4 September 2018

Synthesis (and alternative proof of configuration) of the scyphostatin C(1')-C(20') trienoyl fragment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18593171

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Widely applicable Pd-catalyzed trans-selective monoalkylation of unactivated 1,1-dichloro-1-alkenes and Pd-catalyzed second substitution for the selective synthesis of E or Z trisubstituted alkenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18593171

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A convenient and genuine equivalent to HZrCp2Cl generated in situ from ZrCp2Cl2-DIBAL-H

1 reference

https://pubmed.ncbi.nlm.nih.gov/18593171

12 December 2020

based on heuristic

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Efficient and selective synthesis of siphonarienolone and related reduced polypropionates via Zr-catalyzed asymmetric carboalumination

1 reference

https://pubmed.ncbi.nlm.nih.gov/18593171

12 December 2020

based on heuristic

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Studies directed toward the total synthesis of discodermolide: asymmetric synthesis of the C1-C14 fragment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18593171

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18593171

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antibiotika aus Gleitenden Bakterien, XV. Myaxalamide A, B, C und D eine Gruppe homologer Antibiotika ausMyxococcus xanthus Mx x12 (Myxobacterales)

1 reference

https://opencitations.net/index/api/v1/citations/10.1002/JLAC.198319830702

9 March 2024

Identifiers

10.1021/OL801115S

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

ResearchGate publication ID

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