Complementary Regioselectivity in the Cu(I)-Catalyzed Diamination of Conjugated Dienes To Form Cyclic Sulfamides (Q34543245)

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scientific article published on December 30, 2010

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English	Complementary Regioselectivity in the Cu(I)-Catalyzed Diamination of Conjugated Dienes To Form Cyclic Sulfamides	scientific article published on December 30, 2010

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Complementary regioselectivity in the Cu(I)-catalyzed diamination of conjugated dienes to form cyclic sulfamides (English)

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Complementary Regioselectivity in the Cu(I)-Catalyzed Diamination of Conjugated Dienes To Form Cyclic Sulfamides (English)

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DOI

10.1021/OL102767J

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21 November 2024

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Baoguo Zhao

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2

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2 August 2017

Yian Shi

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21192669

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2 August 2017

Richard G. Cornwall

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1

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21192669

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30 December 2010

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2 August 2017

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21192669

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https://europepmc.org/articles/PMC3031742

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Europe PubMed Central

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Europe PubMed Central

PubMed publication ID

21192669

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21192669

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21 November 2024

https://europepmc.org/articles/PMC3031742?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

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Europe PubMed Central

PubMed publication ID

21192669

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21192669

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21 November 2024

https://doi.org/10.1021/ol102767j

online access status

open access

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Europe PubMed Central

PubMed publication ID

21192669

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21192669

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21 November 2024

https://pubs.acs.org/doi/pdf/10.1021/ol102767j

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DOI

10.1021/OL102767J

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21 November 2024

published in

Organic Letters

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21192669

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2 August 2017

volume

13

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21192669

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2 August 2017

issue

3

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21192669

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2 August 2017

page(s)

434-437

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21192669

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2 August 2017

cites work

Metal-catalysed 1,2-diamination reactions

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Cu(I)-catalyzed regioselective diamination of conjugated dienes via dual mechanistic pathways

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Copper‐Promoted and Copper‐Catalyzed Intermolecular Alkene Diamination

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

An effective C-C double bond formation via Cu(I)-catalyzed dehydrogenation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Synthetic and mechanistic studies on Pd(0)-catalyzed diamination of conjugated dienes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Cu(I)-catalyzed diamination of conjugated olefins with tunable anionic counterions. A possible approach to asymmetric diamination

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

The role of sulfamide derivatives in medicinal chemistry: a patent review (2006-2008)

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

A palladium-catalyzed dehydrogenative diamination of terminal olefins

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Cu(I)-catalyzed asymmetric diamination of conjugated dienes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Catalytic asymmetric allylic and homoallylic diamination of terminal olefins via formal C-H activation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Synthesis and evaluation of sulfamide-type indolizidines as glycosidase inhibitors

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Copper(II) carboxylate promoted intramolecular diamination of terminal alkenes: improved reaction conditions and expanded substrate scope

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Therapeutic potential of sulfamides as enzyme inhibitors.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistry

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

Medicinal agents incorporating the 1,2-diamine functionality

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

7 July 2018

The sulfamide motif in the design of enzyme inhibitors

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Mechanism of N-fluorobenzenesulfonimide promoted diamination and carboamination reactions: divergent reactivity of a Pd(IV) species

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Gold(I)-catalyzed intramolecular dihydroamination of allenes with N,N'-disubstituted ureas to form bicyclic imidazolidin-2-ones

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Synthesis and antibacterial activities of novel oxazolidinones having cyclic sulfonamide moieties

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Direct synthesis of bicyclic guanidines through unprecedented palladium(ii) catalysed diamination with copper chloride as oxidant.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Catalytic diamination of alkenes using N,N-dibromo-p-toluenesulfonamide as electrophile and nitriles as nucleophiles

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Palladium(II)-catalyzed intramolecular diamination of unfunctionalized alkenes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Copper(II) acetate promoted intramolecular diamination of unactivated olefins

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Cyclic sulfamide gamma-secretase inhibitors.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Pd(II)-catalyzed intermolecular 1,2-diamination of conjugated dienes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Electrophilic diamination of alkenes by using FeCl(3)-PPh(3) complex as the catalyst

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

27 October 2018

Palladium-Catalyzed Diamination of Unactivated Alkenes UsingN-Fluorobenzenesulfonimide as Source of Electrophilic Nitrogen

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3031742

retrieved

9 December 2018

Aryl CbondH activation by CuII to form an organometallic aryl-CuIII species: a novel twist on copper disproportionation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine-Tuning the Electronic Properties of Highly Stable Organometallic CuIII Complexes Containing Monoanionic Macrocyclic Ligands

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A facile Pd(0)-catalyzed regio- and stereoselective diamination of conjugated dienes and trienes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Pd(0)-catalyzed diamination of terminal olefins at allylic and homoallylic carbons via formal C-H activation under solvent-free conditions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mild Cu(I)-catalyzed regioselective diamination of conjugated dienes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exploring the nickel-catalyzed oxidation of alkenes: a diamination by sulfamide transfer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric diamination of conjugated dienes and triene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cu(I)-catalyzed intermolecular diamination of activated terminal olefins

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advancing palladium-catalyzed C-N bond formation: bisindoline construction from successive amide transfer to internal alkenes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxidative diamination of alkenes with ureas as nitrogen sources: mechanistic pathways in the presence of a high oxidation state palladium catalyst

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiral tertiary diamines in asymmetric synthesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intramolecular diamination of alkenes with palladium(II)/copper(II) bromide and IPy2BF4: the role of halogenated intermediates

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbon-nitrogen bond formation involving well-defined aryl-copper(III) complexes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis of diamino carboxylic esters by palladium-catalyzed oxidative intramolecular diamination of acrylates

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transition-metal-catalyzed diamination of olefins

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanistic study of copper-catalyzed aerobic oxidative coupling of arylboronic esters and methanol: insights into an organometallic oxidase reaction

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regioselective copper-catalyzed chlorination and bromination of arenes with O(2) as the oxidant

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Chemistry of Vicinal Diamines

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Novel Electrophilic Diamination Reaction of Alkenes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21192669

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereospecific palladium-promoted vicinal diamination of olefins

series ordinal

14

1 reference

stated in

Crossref

DOI

10.1021/OL102767J

reference URL

https://api.crossref.org/works/10.1021/OL102767J

retrieved

21 November 2024

Asymmetric aldol reactions employing a cyclic sulfamide chiral auxiliary

series ordinal

65

1 reference

stated in

Crossref

DOI

10.1021/OL102767J

reference URL

https://api.crossref.org/works/10.1021/OL102767J

retrieved

21 November 2024

Room-temperature aerobic formation of a stable aryl-Cu(III) complex and its reactions with nucleophiles: highly efficient and diverse arene C-H functionalizations of azacalix[1]arene[3]pyridine

series ordinal

71

1 reference

stated in

Crossref

DOI

10.1021/OL102767J

reference URL

https://api.crossref.org/works/10.1021/OL102767J

retrieved

21 November 2024

Identifiers

DOI

10.1021/OL102767J

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21192669

retrieved

2 August 2017

PMC publication ID

3031742

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21192669

retrieved

2 August 2017

PubMed publication ID

21192669

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21192669

retrieved

2 August 2017

ResearchGate publication ID

49715872

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