Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate - Wikidata - awgldk - TriplyDB

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

http://www.wikidata.org/entity/Q28244919

about

Cation-pi control of regiochemistry of intramolecular schmidt reactions en route to bridged bicyclic lactams Total Synthesis and Characterization of 7-Hypoquinuclidonium Tetrafluoroborate and 7-Hypoquinuclidone BF3 Complex Stability of medium-bridged twisted amides in aqueous solutions.Naturally diverse: highlights in versatile synthetic methods enabling target- and diversity-oriented synthesis.Proximity effects in nucleophilic addition reactions to medium-bridged twisted lactams: remarkably stable tetrahedral intermediates.Synthesis of medium-bridged twisted lactams via cation-pi control of the regiochemistry of the intramolecular Schmidt reaction.Synthesis, structural analysis, and reactivity of bridged orthoamides by intramolecular Schmidt reaction Novel tetracyclic structures from the synthesis of thiolactone-isatin hybrids Structural characterization of N-protonated amides: regioselective N-activation of medium-bridged twisted lactams Chemistry of bridged lactams and related heterocycles The stereoselective formation of bicyclic enamines with bridgehead unsaturation via tandem C-H bond activation/alkenylation/electrocyclization.Evolution of a unified, stereodivergent approach to the synthesis of communesin F and perophoramidine.Twisted amide electrophiles enable cyclic peptide sequencing.Radical aryl migration enables diversity-oriented synthesis of structurally diverse medium/macro- or bridged-rings.Origins of regio- and stereochemistry in type 2 intramolecular N-acylnitroso Diels-Alder reactions: a computational study of tether length and substituent effects.Direct synthesis of medium-bridged twisted amides via a transannular cyclization strategy Corey-Chaykovsky epoxidation of twisted amides: synthesis and reactivity of bridged spiro-epoxyamines.Electrospray ionization (ESI) fragmentations and dimethyldioxirane reactivities of three diverse lactams having full, half, and zero resonance energies.Stereoelectronic Chameleons: The Donor-Acceptor Dichotomy of Functional Groups.Cross-coupling of aromatic esters and amides.Structures of Highly Twisted Amides Relevant to Amide N-C Cross-Coupling: Evidence for Ground-State Amide Destabilization.A modular reaction pairing approach to the diversity-oriented synthesis of fused- and bridged-polycyclic sultams.Pyramidalization/twisting of the amide functional group via remote steric congestion triggered by metal coordination.Uncovering the importance of proton donors in TmI2-promoted electron transfer: facile C-N bond cleavage in unactivated amides.An efficient computational model to predict protonation at the amide nitrogen and reactivity along the C-N rotational pathway.Unexpected reactivity and mechanism of carboxamide activation in bacterial N-linked protein glycosylation.Synthesis of cyclic peptides through an intramolecular amide bond rearrangement.Sequential Ruthenium Catalysis for Olefin Isomerization and Oxidation: Application to the Synthesis of Unusual Amino Acids.Experimental and computational studies of anti-Bredt amidinium salts.Nickel-catalyzed transamidation of aliphatic amide derivatives.Enantioselective Catalysis Coupled with Stereodivergent Cyclization Strategies Enables Rapid Syntheses of (+)-Limaspermidine and (+)-Kopsihainanine A.Strain-Induced Reactivity in the Dynamic Covalent Chemistry of Macrocyclic Imines.Twisting the ethano-Tröger's base: the bisamide.Stereoselective and Enantiospecific Mono- and Bis-C-H Azidation of Tröger Bases: Insight on Bridgehead Iminium Intermediates and Application to Anion-Binding Catalysis.Access to divergent benzo-heterocycles via a catalyst-dependent strategy in the controllable cyclization of o-alkynyl-N-methoxyl-benzamides.Palladium-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen cleavage: general strategy for amide N-C bond activation.Oxidative amide synthesis directly from alcohols with amines.Direct room-temperature lactonisation of alcohols and ethers onto amides: an "amide strategy" for synthesis.Sterically-controlled intermolecular Friedel-Crafts acylation with twisted amides via selective N-C cleavage under mild conditions.Structural Characterization of N-Alkylated Twisted Amides: Consequences for Amide Bond Resonance and N-C Cleavage.

P2860

Q24649642-784BAC6C-B14F-44B3-B801-808D8F006E9B Q28833569-82A24BE8-794E-4192-83ED-0CE709929D11 Q33403839-F27CC0B7-1612-4C89-BE31-80E4CE5B1EB6 Q33431379-7921A9F7-94B1-4BD2-BBC9-D1675BB6BDDC Q33645856-11A04B5F-B16B-40E1-9D94-11D37C0C0FFE Q33651096-E3038D7F-B139-45B4-9731-DFC66DD3B592 Q33688059-ADD1F795-3530-4420-BC76-ACFB3A6AC3F9 Q34056494-2093A648-B50B-41A8-95BB-71740BEB0483 Q34059786-B36912CB-EC76-41DB-90EA-2613CA7AA52B Q34138748-D38E8280-88BD-4A36-9520-D4F44108B7F3 Q34711188-2E5D3078-79A0-4538-A5E5-147076020129 Q34841311-5A3884BA-5601-4E44-A79A-C5221CF7864C Q35664642-0B7F181D-B941-4791-A14D-557CD5EFAC19 Q36231032-ECD1EDC4-D721-4278-B0A3-6101C0003366 Q36802661-3C491327-28B5-4D4D-ADB3-F1EFDA853430 Q37326098-89C3F0A2-CD2E-447A-9981-2620C6780B7E Q37367310-1C20F6B5-3851-428A-A9D5-5BE04BE9B5A8 Q37649398-9AFACB7E-304C-45D5-A817-6DD08F84C6AC Q39013020-78BB1FA0-7930-4BEA-9AF3-5FA6A355D048 Q39420428-4D5C71A4-2E3B-4BCD-B04C-35DFFDF9E3E2 Q39456502-40E180D5-A35C-4B81-B609-C36B7DC7768D Q40838939-DB9A2941-D3A2-46D1-9869-B92335CE248A Q41828180-E1327560-1D00-40D4-A1F1-03CFACBEED1D Q41842269-C3C0C98D-BD30-4255-8C43-C95C9F1F9E1F Q42663913-B7A7314B-CF86-4F4C-8FC9-B0E1682CFDC2 Q44423772-D5C41D4D-98E8-4858-A23A-52AB378B9D5E Q45156268-C7E3324F-84DB-427C-BCBF-CC0D04A04531 Q46073254-C36E6DD0-E5DD-4922-98E5-0BF202C23D7F Q46116229-B364337B-B99E-4F31-9CC1-5F01D95840B4 Q46184383-016D2340-81A6-4C1D-8588-957968CDC47F Q46203531-53556884-9894-4A6A-A08F-A3215AB033A2 Q46716743-605212EC-D0B3-4E52-849F-1CC09334CDA6 Q48157586-789C095F-7DAB-4E95-85A1-C95B6927F004 Q48279922-BBEB0459-75D6-4C8C-AA12-FF057880DB65 Q50203046-36C1FBB7-0C10-4E7A-AE45-01D0F1AE91B6 Q50881725-3707B545-3120-4915-9F03-8244275EEE74 Q51639112-B618B6A9-0A28-4D07-A058-016FF80DED90 Q51838871-D8B114D6-F6F4-41D0-AD8E-3713C7F13E10 Q52871701-9083D674-CDC4-4C3A-8988-3FDD8FEDB1DE Q52881703-54BDD8F6-9550-4B0E-B16C-FEE1257853DF

P2860

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

http://www.wikidata.org/entity/Q28244919

description

2006 nî lūn-bûn

@nan

2006 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@ast

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@en

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@nl

type

label

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@ast

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@en

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@nl

prefLabel

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@ast

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@en

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@nl

P1433

Q28244919-22BD0EB5-BA1C-4B2E-9C56-2F400233072B

P1476

Q28244919-1C46A1E9-8B8A-4660-92F6-14D42FE7C2D4

P2093

Q28244919-A2CDD3DF-63DF-468E-8393-31C48AF73C99

Q28244919-E457F664-F2E4-4D11-B461-64EBC9A77BAD

P2860

Q28244919-5AFB43E2-5DAD-474B-8FB6-337E17AEDAAC

Q28244919-74E562EC-279C-46F8-9653-982182C329BE

Q28244919-7B18F740-0DAE-4A99-B0AB-32D006612935

Q28244919-83EB11A0-C817-4D3A-BC9B-673DCD7490D7

Q28244919-8E35841D-1B62-45DD-BFEC-83C4E60FDE0E

Q28244919-9A606FF0-268D-4E39-BDEB-4B70D0807013

P2888

Q28244919-6CE03F7C-6FB4-4F68-A788-D4B1113154C9

P304

Q28244919-6EF65F0D-85BD-4F5B-B429-5C94B42ECE43

P31

Q28244919-5E910DB2-1724-442C-9DEB-CB1B8759820E

P356

Q28244919-1A1F056F-5BFC-48B7-A47C-68119EC4D9CA

P407

Q28244919-511FFFD7-D898-4FC7-8ABE-88822EAB30D9

P433

Q28244919-833404B9-824A-44FA-9F6F-8C74A52D1ACC

P478

Q28244919-ACF687D7-DE83-42E7-BC57-34BC82935DFA

P577

Q28244919-584797CD-DEA1-4108-9BFF-E83FBBE215B4

P5875

Q28244919-58CCB65F-3937-473A-9019-4340A461ED06

P6179

Q28244919-97B13EAA-677D-4229-8749-02FA3A9BEF8D

P698

Q28244919-620CBA36-6044-4A99-801F-6035EEECB3E1

P356

P1433

P1476

Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate

@en

P2093

Brian M Stoltz

http://www.w3.org/2001/XMLSchema#string

Kousuke Tani

http://www.w3.org/2001/XMLSchema#string

P2860

Cloning, expression, and purification of human cyclophilin in Escherichia coli and assessment of the catalytic role of cysteines by site-directed mutagenesis

Structural insights into the protein splicing mechanism of PI-SceI

Semisynthesis of a segmental isotopically labeled protein splicing precursor: NMR evidence for an unusual peptide bond at the N-extein-intein junction.

Über sterische Hinderung in Brückenringen (Bredtsche Regel) und über diemeso-trans-Stellung in kondensierten Ringsystemen des Hexamethylens

Facile C−N Cleavage in a Series of Bridged Lactams

Intramolecular Schmidt reaction of alkyl azides

P2888

P304

731-4

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/NATURE04842

http://www.w3.org/2001/XMLSchema#string

P407

P433

7094

http://www.w3.org/2001/XMLSchema#string

P478

441

http://www.w3.org/2001/XMLSchema#string

P577

2006-06-08T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

7022221

http://www.w3.org/2001/XMLSchema#string

P6179

1032034038

http://www.w3.org/2001/XMLSchema#string

P698

16760973

http://www.w3.org/2001/XMLSchema#string