(Q34255322)

English

Highly stereoselective and scalable anti-aldol reactions using N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: scope and origins of stereoselectivities

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Highly stereoselective and scalable anti-aldol reactions using N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: scope and origins of stereoselectivities (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

stereoselectivity

1 reference

based on heuristic

inferred from title

Paul Ha-Yeon Cheong

3

object named as

Paul Ha-Yeon Cheong

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Hua Yang

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Subham Mahapatra

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Rich G Carter

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

0 references

publication date

1 November 2010

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Journal of Organic Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

75

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

21

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

7279-7290

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Organocatalytic cascade reactions as a new tool in total synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

"Try and fall sick .."-the composer, chemist, and surgeon Aleksandr Borodin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Development of an enantioselective route toward the Lycopodium alkaloids: total synthesis of lycopodine.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

The direct catalytic asymmetric aldol reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Organocatalytic reactions in water

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Structure determination and absolute configuration of cannabichromanone derivatives from high potency Cannabis sativa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Total synthesis of auripyrone A using a tandem non-aldol aldol/Paterson aldol process as a key step

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Organocatalysis--after the gold rush

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Asymmetric catalysis with chiral primary amine-based organocatalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Asymmetric organocatalysis by chiral Brønsted bases: implications and applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: a practical proline mimetic for facilitating enantioselective aldol reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

The advent and development of organocatalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Asymmetric aminocatalysis--gold rush in organic chemistry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Catalytic asymmetric aldol reactions in aqueous media

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Asymmetric organocatalysis: from infancy to adolescence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Organocatalysed asymmetric Mannich reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Asymmetric enamine catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Critical assessment of pharmaceutical processes--A rationale for changing the synthetic route

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

The Lycopodium alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Highly anti-selective asymmetric aldol reactions using chiral zirconium catalysts. Improvement of activities, structure of the novel zirconium complexes, and effect of a small amount of water for the preparation of the catalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Diastereoselective magnesium halide-catalyzed anti-aldol reactions of chiral N-acyloxazolidinones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Proline-catalyzed asymmetric aldol reactions between ketones and alpha-unsubstituted aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Chiral bis(oxazoline) copper(II) complexes: versatile catalysts for enantioselective cycloaddition, Aldol, Michael, and carbonyl ene reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

6 July 2018

Synthesis of all-carbon, quaternary center-containing cyclohexenones through an organocatalyzed, multicomponent coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Amide-based bifunctional organocatalysts in asymmetric reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Polyketide building blocks via diastereoselective nitrile oxide cycloadditions with homoallylic alcohols and monoprotected homoallylic diols

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Anti and syn glycolate aldol reactions with a readily displaced thiol auxiliary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Origins of the double asymmetric induction on proline-catalyzed aldol reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Enantioselective synthesis of (R)-convolutamydine A with new N-heteroarylsulfonylprolinamides.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Lewis base activation of Lewis acids: catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

1,5-anti stereocontrol in the boron-mediated aldol reactions of beta-alkoxy methyl ketones: the role of the formyl hydrogen bond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Highly efficient asymmetric direct stoichiometric aldol reactions on/in water

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Highly diastereo- and enantioselective direct aldol reactions of aldehydes and ketones catalyzed by siloxyproline in the presence of water

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Piperylene sulfone: a labile and recyclable DMSO substitute.

1 reference

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28 October 2018

Potential cancer chemopreventive in vitro activities of monomeric xanthone derivatives from the marine algicolous fungus Monodictys putredinis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Highly diastereo- and enantioselective direct aldol reactions in water.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

A highly efficient organocatalyst for direct aldol reactions of ketones with aldehydes [corrected].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

A pentenyl dianion-based strategy for convergent synthesis of ene-1,5-diols

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

A SuperQuat glycolate aldol approach to the asymmetric synthesis of hexose monosaccharides.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Computational evidence for the enamine mechanism of intramolecular aldol reactions catalyzed by proline

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Enantioselective total synthesis of (+)-gigantecin: exploiting the asymmetric glycolate aldol reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Theoretical study of the stereoselective additions of chiral alcohols to ketenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Theory of asymmetric organocatalysis of Aldol and related reactions: rationalizations and predictions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Total Synthesis of (+)-Geldanamycin and (−)-o-Quinogeldanamycin: Asymmetric Glycolate Aldol Reactions and Biological Evaluation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Novel Small Organic Molecules for a Highly Enantioselective Direct Aldol Reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

Quantum mechanical predictions of the stereoselectivities of proline-catalyzed asymmetric intermolecular aldol reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

The origin of diastereofacial control in allylboration reactions using tartrate ester derived allylboronates: attractive interactions between the Lewis acid coordinated aldehyde carbonyl group and an ester carbonyl oxygen

1 reference

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28 October 2018

Magnitudes and chemical consequences of R(3)N(+)-C-H...O[double bond]C hydrogen bonding

1 reference

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28 October 2018

The origin of stereoselectivity in proline-catalyzed intramolecular aldol reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2966945

28 October 2018

First enantioselective synthesis of (R)-convolutamydine B and E with N-(heteroarenesulfonyl)prolinamides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regiospecific organocatalytic asymmetric aldol reaction of methyl ketones and alpha,beta-unsaturated trifluoromethyl ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unusual homoisoflavanone and a structurally-related dihydrochalcone from Polygonum ferrugineum (Polygonaceae)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly diastereoselective anti-aldol reactions utilizing the titanium enolate of cis-2-arylsulfonamido-1- acenaphthenyl propionate

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric glycolate aldol reactions using cinchonium phase-transfer catalysts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly efficient and reusable dendritic catalysts derived from N-prolylsulfonamide for the asymmetric direct aldol reaction in water

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The thiopyran route to polypropionates: enantioselective synthesis of membrenone B from racemic fragments.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Understanding the Origins of Remote Asymmetric Induction in the Boron Aldol Reactions of β-Alkoxy Methyl Ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Lycopodium alkaloids

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sterically and electronically tunable and bifunctional organocatalysts: design and application in asymmetric aldol reaction of cyclic ketones with aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiral Phosphoramide-Catalyzed Aldol Additions of Ketone Trichlorosilyl Enolates. Mechanistic Aspects

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https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

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Proline-catalyzed asymmetric addition reaction of 9-tosyl-3,4-dihydro-beta-carboline with ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

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Synthetic studies on siphonariid polypropionates: synthesis and isomerization of the caloundrin B trioxaadamantane ring system

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https://pubmed.ncbi.nlm.nih.gov/20932013

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A rationale for determining, testing, and controlling specific impurities in pharmaceuticals that possess potential for genotoxicity

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly diastereoselective anti-aldol reactions of glycolate titanium enolates

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective organocatalytic aldol reaction of ynones and its synthetic applications

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C2-symmetric bisprolinamide as a highly efficient catalyst for direct aldol reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water

1 reference

https://pubmed.ncbi.nlm.nih.gov/20932013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JO1015008

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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