(Q33823837)

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Diverging DOS strategy using an allene-containing tryptophan scaffold and a library design that maximizes biologically relevant chemical space while minimizing the number of compounds

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Europe PubMed Central

PubMed publication ID

29 July 2017

Diverging DOS strategy using an allene-containing tryptophan scaffold and a library design that maximizes biologically relevant chemical space while minimizing the number of compounds (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Kay M. Brummond

5

object named as

Kay M Brummond

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Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Thomas O Painter

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Lirong Wang

2

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Europe PubMed Central

PubMed publication ID

29 July 2017

Supriyo Majumder

3

1 reference

Europe PubMed Central

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29 July 2017

Xiang-Qun Xie

4

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Europe PubMed Central

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29 July 2017

publication date

18 February 2011

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29 July 2017

ACS combinatorial science

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Europe PubMed Central

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29 July 2017

13

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Europe PubMed Central

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29 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

166-174

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Spiroindolones, a potent compound class for the treatment of malaria

1 reference

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28 July 2018

Current strategies for diversity-oriented synthesis

1 reference

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Synthesis of natural-product-like molecules with over eighty distinct scaffolds

1 reference

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Data mining a small molecule drug screening representative subset from NIH PubChem

1 reference

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Towards the optimal screening collection: a synthesis strategy

1 reference

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28 July 2018

Design and synthesis of a 3,4-dehydroproline amide discovery library

1 reference

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28 July 2018

Rhodium(I)-catalyzed allenic carbocyclization reaction affording delta- and epsilon-lactams

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

28 July 2018

Chemistry and biology of monoterpene indole alkaloid biosynthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

28 July 2018

Solution-phase synthesis of a tricyclic pyrrole-2-carboxamide discovery library applying a stetter-Paal-Knorr reaction sequence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

28 July 2018

Diversity-oriented synthesis: exploring the intersections between chemistry and biology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

28 July 2018

Heterocyclic alpha-alkylidene cyclopentenones obtained via a Pauson-Khand reaction of amino acid derived allenynes. A scope and limitation study directed toward the preparation of a tricyclic pyrrole library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

28 July 2018

Molecular shape diversity of combinatorial libraries: a prerequisite for broad bioactivity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

28 July 2018

Differentiating mechanistic possibilities for the thermal, intramolecular [2 + 2] cycloaddition of allene-ynes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

29 October 2018

Rh(I)-catalyzed cyclocarbonylation of allenol esters to prepare acetoxy 4-alkylidenecyclopent-3-en-2-ones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

29 October 2018

Silver-mediated synthesis of heterocycles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

29 October 2018

Structural diversity of organic chemistry. A scaffold analysis of the CAS Registry.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

29 October 2018

Reaction of alpha-(N-carbamoyl)alkylcuprates with propargyl substrates: synthetic route to alpha-amino allenes and delta3-pyrrolines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3104414

29 October 2018

Synthesis of 3-pyrrolines, annulated 3-pyrrolines, and pyrroles from alpha-amino allenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21332123

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

1 reference

https://pubmed.ncbi.nlm.nih.gov/21332123

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allenes and transition metals: a diverging approach to heterocycles

1 reference

https://pubmed.ncbi.nlm.nih.gov/21332123

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microwave-assisted intramolecular [2 + 2] Allenic cycloaddition reaction for the rapid assembly of bicyclo[4.2.0]octa-1,6-dienes and bicyclo[5.2.0]nona-1,7-dienes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21332123

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reaction of alpha-(N-carbamoyl)alkylcuprates with enantioenriched propargyl electrophiles: synthesis of enantioenriched 3-pyrrolines

1 reference

https://pubmed.ncbi.nlm.nih.gov/21332123

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/CO100052S

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Europe PubMed Central

PubMed publication ID

29 July 2017

release_lzuribku3rakrn3sb2v7v7j63y

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https://api.fatcat.wiki/v0/release/lzuribku3rakrn3sb2v7v7j63y

24 November 2022

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PMC publication ID

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Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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