Reaction of oxazoles with the methyl ester of acetylenedicarboxylic acid

Kondrat'eva, G. Ya.; Medvedskaya, L. B.; Ivanova, Z. N.

doi:10.1007/bf00851268

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Oxazole-jv-oxides1

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1974

1998

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Cited by 3 publications

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“…1,3-Dipolar addition of the acetylene to 533 followed by 1,3-dipolar cycloreversion of carbon dioxide from the initially formed adduct 539 gives the pyrrole derivatives 540. Some recently reported examples of this process are given in eq [198][199][200][201][202].…”

Section: Oxazole-jv-oxidesmentioning

confidence: 99%

Oxazole chemistry. A review of recent advances

Turchi¹

1981

Ind. Eng. Chem. Prod. Res. Dev.

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Section: Oxazole-jv-oxidesmentioning

confidence: 99%

Oxazole chemistry. A review of recent advances

Turchi¹

1981

Ind. Eng. Chem. Prod. Res. Dev.

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The Retro–Diels–Alder Reaction PartII. Dienophiles with One or More Heteroatom

Rickborn

1998

Organic Reactions

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This review (Part II) is topically organized around the dienophile that is generated in a retro [4 + 2] reaction, and to the extent possible follows the principles adopted for Part I, which covers reactions in which both dienophile bonding centers are carbon atoms. The present chapter encompasses retro–Diels–Alder (rDA) reactions in which one or both of the dienophile reaction centers are heteroatoms. Any of the other atoms in the starting material (cycloadduct) may be carbon or heteroatom. Substituents on all positions are encompassed, and any bond order available to any oxidation state of an element is included, as is bonding to non‐nearest neighbor atoms (e.g., bicyclics). The reader is directed to Part I (Vol. 52) for general discussion of the rDA reaction, the features that affect rates and outcome, and the use of acids, bases, other catalysts, and scavengers. Certain subclassifications (e.g., processes proposed under MS conditions, polymer applications) of rDA reactions have been omitted from both sections; these topics are listed in the Introduction to Part I. Citations to over 100 reviews on various aspects of the rDA reaction are collected at the beginning of the References to Part I. Those that are especially pertinent to Part II will be repeated here, in the context of the particular dienophile under discussion. The decision to split the review of the rDA reaction into two parts was based on the volume of literature encountered, as outlined in the Introduction to Part I. Active literature searching was concluded for both Parts in April 1995, although occasional more recent references have been included.

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Advances in Oxazole Chemistry

Lakhan

Ternai

1974

Advances in Heterocyclic Chemistry

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Reaction of oxazoles with the methyl ester of acetylenedicarboxylic acid

Cited by 3 publications

References 3 publications

Oxazole chemistry. A review of recent advances

Oxazole chemistry. A review of recent advances

The Retro–Diels–Alder Reaction PartII. Dienophiles with One or More Heteroatom

Advances in Oxazole Chemistry

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