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Journal ArticleDOI

Effect of catalyst on zwitterionic intermediacy in additions of dimethyl diazomalonate to vinyl ethers

Miguel E. Alonso, +1 more
- 01 Jan 1989 - 
- Vol. 45, Iss: 11, pp 3313-3320
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TLDR
In this paper, the reaction of dimethyl diazomalonate with 2-alkoxy-6-methyl-3,4-dihydro-2H-pyran in hot fluorobenzene has been studied in the presence of some transition metal catalysts.
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This article is published in Tetrahedron.The article was published on 1989-01-01. It has received 18 citations till now. The article focuses on the topics: Carbenium ion & Pyran.

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Journal ArticleDOI

Chiral catalysts for enantioselective carbenoid cyclopropanation reactions

TL;DR: In this article, the major advances in chiral catalyst design and development are described, and a uniform mechanistic interpretation is advanced to explain the results accumulated in reported investigations, focusing on chiral salicylaldimine and semicorrin/bis-oxazoline copper catalysts and on the newest class of chiral catalysts for enantioselective carbenoid reactions.
Reference EntryDOI

Intermolecular Metal‐Catalyzed Carbenoid Cyclopropanations

TL;DR: The metal-catalyzed decomposition of diazo compounds in the presence of alkenes is a well-established reaction as mentioned in this paper, and it has been recognized that a wide array of carbenoid structures can be utilized in this chemistry, leading to a broad range of synthetic applications.
Journal ArticleDOI

Highly Enantioselective Intramolecular Cyclopropanation Reactions of N-Allylic-N-methyldiazoacetamides Catalyzed by Chiral Dirhodium(II) Carboxamidates

TL;DR: In this paper, dirhodium(II) tetrakis[methyl 2-oxo-1-(3-phenylpropanoyl)imidazolidin-4(S)-carboxylate], Rh2(4S)-MPPIM)4 was preferred for substituted N-allylic-N-methyldiazoacetamides from which 92−95% ee's were obtained in intramolecular cyclopropanation reactions (88−95 percent yields), even when the catalyst was employed in only 0.
Journal ArticleDOI

Dirhodium(II) Tetracarboxylate carbenoids as catalytic intermediates

TL;DR: In this article, a more detailed mechanistic study of rh 2 (O 2 CR) 4 catalysis is presented, with significant participation by the backside of the Rh atom.
References
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Catalytic methods for metal carbene transformations

TL;DR: Doyle et al. as discussed by the authors used transition-metal catalysts to generate transient electrophilic metal carhenes and achieved state-of-the-art performance on the Dreyfus Foundation Teacher-Scholar Award and Chemical Manufacturers Association Catalyst Award.
Journal ArticleDOI

Multiple metal-carbon bonds. 43. Well-characterized, highly active, Lewis acid free olefin metathesis catalysts

TL;DR: In this article, a complexe de W de type W(CH−t−Bu)(NR)(OR') 2, OR'=OC(Me)(CF 3 ) 2
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