(Q42578611)

English

Study of the cis to trans isomerization of 1-phenyl-2,3-disubstituted tetrahydro-beta-carbolines at C(1). Evidence for the carbocation-mediated mechanism

scientific article published on April 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

Study of the cis to trans isomerization of 1-phenyl-2,3-disubstituted tetrahydro-beta-carbolines at C(1). Evidence for the carbocation-mediated mechanism (English)

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

Jeffrey R. Deschamps

5

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

author name string

Hephzibah J Kumpaty

1

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

Michael L Van Linn

2

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

M Shahjahan Kabir

3

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

F Holger Försterling

4

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

James M Cook

6

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

language of work or name

0 references

publication date

1 April 2009

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

Journal of Organic Chemistry

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

74

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

7

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

2771-2779

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

Weak Brønsted acid-thiourea co-catalysis: enantioselective, catalytic protio-Pictet-Spengler reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

28 May 2018

Enantioselective thiourea-catalyzed additions to oxocarbenium ions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

28 May 2018

An improved total synthesis of (+)-macroline and alstonerine as well as the formal total synthesis of (-)-talcarpine and (-)-anhydromacrosalhine-methine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

28 May 2018

GABA(A) and opioid receptors of the central nucleus of the amygdala selectively regulate ethanol-maintained behaviors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

28 May 2018

General approach for the synthesis of sarpagine/ajmaline indole alkaloids. Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

28 May 2018

Enantioselective BINOL-phosphoric acid catalyzed Pictet-Spengler reactions of N-benzyltryptamine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Total synthesis of the opioid agonistic indole alkaloid mitragynine and the first total syntheses of 9-methoxygeissoschizol and 9-methoxy-Nb-methylgeissoschizol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Catalytic asymmetric Pictet-Spengler reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Highly enantioselective catalytic acyl-pictet-spengler reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Solid-phase synthesis of 1-substituted tetrahydroisoquinoline derivatives employing BOC-protected tetrahydroisoquinoline carboxylic acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Solid-phase intramolecular N-acyliminium Pictet-Spengler reactions as crossroads to scaffold diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Stereocontrolled total synthesis of (-)-vincamajinine and (-)-11-methoxy-17-epivincamajine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Enantiospecific total synthesis of (-)-(E)16-epiaffinisine, (+)-(E)16-epinormacusine B, and (+)-dehydro-16-epiaffinisine as well as the stereocontrolled total synthesis of alkaloid G.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

The GABA(A) receptor alpha1 subtype in the ventral pallidum regulates alcohol-seeking behaviors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Enantiospecific Formation of Trans 1,3-Disubstituted Tetrahydro-beta-carbolines by the Pictet-Spengler Reaction and Conversion of Cis Diastereomers into Their Trans Counterparts by Scission of the C-1/N-2 Bond.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2758420

16 August 2018

Enantiopure Tetrahydro-β-carbolines via Pictet−Spengler Reactions withN-Sulfinyl Tryptamines

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric Pictet-Spengler reactions via sulfenyliminium ions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantiospecific total synthesis of the sarpagine related indole alkaloids talpinine and talcarpine as well as the improved total synthesis of alstonerine and anhydromacrosalhine-methine via the asymmetric Pictet-Spengler reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regiospecific, Enantiospecific Total Synthesis of the Alkoxy-Substituted Indole Bases, 16-epi-Na-Methylgardneral, 11-Methoxyaffinisine, and 11-Methoxymacroline as Well as the Indole Alkaloids Alstophylline and Macralstonine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The acid catalysed C3 epimerization of reserpine and deserpidine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiral Lewis Acid-Mediated Enantioselective Pictet-Spengler Reaction of N(b)-Hydroxytryptamine with Aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conformational analysis of the cis- and trans-adducts of the Pictet - Spengler reaction. Evidence for the structural basis for the C(1) - N(2) scission process in the cis- to trans-isomerization

1 reference

https://pubmed.ncbi.nlm.nih.gov/19275130

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JO8028168

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

3 November 2017

ResearchGate publication ID

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