Catalytic asymmetric generation of (Z)-disubstituted allylic alcohols (Q36868019)

16 August 2017

Catalytic asymmetric generation of (Z)-disubstituted allylic alcohols (English)

1 reference

16 August 2017

Luca Salvi

1

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16 August 2017

Sang-Jin Jeon

2

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16 August 2017

Ethan L Fisher

3

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16 August 2017

Patrick J Carroll

4

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16 August 2017

Patrick J Walsh

5

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16 August 2017

language of work or name

English

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publication date

4 December 2007

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16 August 2017

7

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Journal of the American Chemical Society

inferred from page(s)

published in

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16 August 2017

129

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16 August 2017

51

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16 August 2017

16119-16125

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From aryl bromides to enantioenriched benzylic alcohols in a single flask: Catalytic asymmetric arylation of aldehydes

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Catalytic asymmetric approaches towards enantiomerically enriched diarylmethanols and diarylmethylamines

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

A positional scanning approach to the discovery of dipeptide-based catalysts for the enantioselective addition of vinylzinc reagents to aldehydes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Stereoselective cyclopropanation reactions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

A general, highly enantioselective method for the synthesis of D and L alpha-amino acids and allylic amines

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Highly enantioselective direct reductive coupling of conjugated alkynes and alpha-ketoesters via rhodium-catalyzed asymmetric hydrogenation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

A green chemistry approach to a more efficient asymmetric catalyst: solvent-free and highly concentrated alkyl additions to ketones

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Enantioselective addition of vinylzinc reagents to aldehydes catalyzed by modular ligands derived from amino acids

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Highly enantio- and diastereoselective one-pot synthesis of acyclic epoxy alcohols and allylic epoxy alcohols

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Highly enantio- and diastereoselective tandem generation of cyclopropyl alcohols with up to four contiguous stereocenters

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Catalytic asymmetric vinylation and dienylation of ketones

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

One-pot asymmetric synthesis of acyclic chiral epoxy alcohols via tandem vinylation-epoxidation with dioxygen

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Highly enantio- and diastereoselective one-pot synthesis of acyclic epoxy alcohols with three contiguous stereocenters

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Catalytic asymmetric vinylation of ketones

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

A phosphorimidate rearrangement for the facile and selective preparation of allylic amines

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Asymmetric addition of alkylzinc reagents to cyclic alpha,beta-unsaturated ketones and a tandem enantioselective addition/diastereoselective epoxidation with dioxygen

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Catalytic asymmetric reductive coupling of alkynes and aldehydes: enantioselective synthesis of allylic alcohols and alpha-hydroxy ketones

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

The MPEG effect: improving asymmetric processes by simple additives

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2532596

Asymmetric Ni(II)/Cr(II)-mediated coupling reaction: stoichiometric process

20 October 2018

1 reference

12 December 2020

New reagents for stereoselective carbonyl reduction. Improved synthetic route to the primary prostaglandins

1 reference

12 December 2020

A catalytic asymmetric method for the synthesis of gamma-unsaturated beta-amino acid derivatives

1 reference

12 December 2020

Strategies for expanding structural diversity available from olefin isomerization-claisen rearrangement reactions

1 reference

12 December 2020

1 reference

12 December 2020

Highly regioselective, catalytic asymmetric reductive coupling of 1,3-enynes and ketones

1 reference

12 December 2020

Acid-Base Adducts of Catalytically Active Titanium(IV) Lewis Acids

1 reference

12 December 2020

Nickel-catalyzed cyclizations, couplings, and cycloadditions involving three reactive components

1 reference

12 December 2020

Direct, stereospecific generation of (Z)-disubstituted allylic alcohols

1 reference

12 December 2020

A one-pot multicomponent coupling reaction for the stereocontrolled synthesis of (Z)-trisubstituted allylic alcohols

1 reference

12 December 2020

Identifiers

DOI

10.1021/JA0762285

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16 August 2017

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16 August 2017

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