Preparation of oxazoline N-oxides and imidate N-oxides by amide acetal condensation and their [3+2] cycloaddition reactions

Stephen P. Ashburn; Robert M. Coates

doi:10.1021/jo00217a013

Preparation of oxazoline N-oxides and imidate N-oxides by amide acetal condensation and their [3+2] cycloaddition reactions

The Journal of Organic Chemistry ◽

10.1021/jo00217a013 ◽

1985 ◽

Vol 50 (17) ◽

pp. 3076-3081 ◽

Cited By ~ 23

Author(s):

Stephen P. Ashburn ◽

Robert M. Coates

Keyword(s):

Cycloaddition Reactions ◽

Amide Acetal ◽

Acetal Condensation

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ChemInform Abstract: Preparation of Oxazoline N-Oxides and Imidate N-Oxides by Amide Acetal Condensation and Their [3 + 2] Cycloaddition Reactions.

Chemischer Informationsdienst ◽

10.1002/chin.198612241 ◽

1986 ◽

Vol 17 (12) ◽

Author(s):

S. P. ASHBURN ◽

R. M. COATES

Keyword(s):

Cycloaddition Reactions ◽

Amide Acetal ◽

Acetal Condensation

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The amide acetal condensation of propargyl alcohols: synthesis of γ-keto esters and silyl allenes under mild conditions

Tetrahedron Letters ◽

10.1016/s0040-4039(00)93726-2 ◽

1976 ◽

Vol 17 (5) ◽

pp. 341-344 ◽

Cited By ~ 12

Author(s):

Kathlyn A. Parker ◽

Raymond W. Kosley

Keyword(s):

Keto Esters ◽

Mild Conditions ◽

Amide Acetal ◽

Acetal Condensation ◽

Propargyl Alcohols

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ChemInform Abstract: THE AMIDE ACETAL CONDENSATION OF PROPARGYL ALCOHOLS. SYNTHESIS OF Γ-KETO ESTERS AND SILYL ALLENES UNDER MILD CONDITIONS

Chemischer Informationsdienst ◽

10.1002/chin.197616149 ◽

1976 ◽

Vol 7 (16) ◽

pp. no-no

Author(s):

K. A. PARKER ◽

R. W. JUN. KOSLEY

Keyword(s):

Keto Esters ◽

Mild Conditions ◽

Amide Acetal ◽

Acetal Condensation ◽

Propargyl Alcohols

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Cycloaddition Reactions in Carbohydrate Chemistry

10.1021/bk-1992-0494 ◽

1992 ◽

Cited By ~ 5

Keyword(s):

Cycloaddition Reactions ◽

Carbohydrate Chemistry

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INTRAMOLECULAR CATIONIC [5 + 2] CYCLOADDITION REACTIONS PROMOTED BY TRIMETHYLSILYL TRIFLATE IN 3.0 M LITHIUM PERCHLORATE-ETHYL ACETATE: APPLICATION TO A FORMAL TOTAL SYNTHESIS OF (±)-ISOCOMENE

Tetrahedron ◽

10.1016/s0040-4020(97)00581-4 ◽

1997 ◽

Vol 53 (26) ◽

pp. 8975-8996

Author(s):

P Grieco*

Keyword(s):

Total Synthesis ◽

Ethyl Acetate ◽

Lithium Perchlorate ◽

Cycloaddition Reactions

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Multicomponent 1,3-Dipolar Cycloaddition Reactions in the Construction of Hybrid Spiroheterocycles

Current Organic Chemistry ◽

10.2174/13852728113179990091 ◽

2013 ◽

Vol 17 (18) ◽

pp. 1929-1956 ◽

Cited By ~ 16

Author(s):

Natarajan Arumugam ◽

Raju Kumar ◽

Abdulrahman Almansour ◽

Subbu Perumal

Keyword(s):

Dipolar Cycloaddition ◽

Cycloaddition Reactions

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Graphene in Copper Catalyzed Azide-Alkyne Cycloaddition Reactions: Evolution from [60]Fullerene and Carbon Nanotubes Strategies

Current Organic Chemistry ◽

10.2174/1385272811317150017 ◽

2013 ◽

Vol 17 (15) ◽

pp. 1680-1693 ◽

Cited By ~ 11

Author(s):

Jose Segura ◽

Horacio Salavagione

Keyword(s):

Carbon Nanotubes ◽

Cycloaddition Reactions

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Synthesis of New Aryl(Hetaryl)-Substituted Tandospirones Under Reductive Heck Type Hydroarylations and Isoxazoline Derivatives via 1,3-Dipolar Cycloaddition Reactions with Expected Anxiolytic Activity†

Current Organic Synthesis ◽

10.2174/1570179411310030010 ◽

2013 ◽

Vol 10 (3) ◽

pp. 481-485 ◽

Cited By ~ 2

Author(s):

Irem Kulu ◽

Asli Kopruceli ◽

Gokce Goksu ◽

Nuket Ocal

Keyword(s):

Anxiolytic Activity ◽

Dipolar Cycloaddition ◽

Cycloaddition Reactions

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Transition Metal-Catalyzed [2+2] Cycloaddition Reactions between Bicyclic Alkenes and Alkynes

Current Organic Synthesis ◽

10.2174/157017909788921907 ◽

2009 ◽

Vol 6 (3) ◽

pp. 219-238 ◽

Cited By ~ 23

Author(s):

William Tam ◽

Jordan Goodreid ◽

Neil Cockburn

Keyword(s):

Transition Metal ◽

Cycloaddition Reactions ◽

Transition Metal Catalyzed ◽

Metal Catalyzed

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Preparation of Fluorine-Containing Heterocyclic Compounds via Cycloaddition Reactions

Mini-Reviews in Organic Chemistry ◽

10.2174/1570193043403064 ◽

2004 ◽

Vol 1 (4) ◽

pp. 417-435 ◽

Cited By ~ 7

Author(s):

P. He ◽

S. Zhu

Keyword(s):

Heterocyclic Compounds ◽

Cycloaddition Reactions

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