A DFT Study of the Domino Inter [4 + 2]/Intra [3 + 2] Cycloaddition Reactions of Nitroalkenes with Enol Ethers

Luis R. Domingo; Amparo Asensio

doi:10.1021/jo991507z

A DFT Study of the Domino Inter [4 + 2]/Intra [3 + 2] Cycloaddition Reactions of Nitroalkenes with Enol Ethers

The Journal of Organic Chemistry ◽

10.1021/jo991507z ◽

2000 ◽

Vol 65 (4) ◽

pp. 1076-1083 ◽

Cited By ~ 21

Author(s):

Luis R. Domingo ◽

Amparo Asensio

Keyword(s):

Dft Study ◽

Cycloaddition Reactions ◽

Enol Ethers

Triplex-catalyzed diels-alder and [2+2] cycloaddition reactions of enol ethers and ketene acetals

Tetrahedron Letters ◽

10.1016/s0040-4039(00)80697-8 ◽

1988 ◽

Vol 29 (40) ◽

pp. 5125-5128 ◽

Cited By ~ 8

Author(s):

Nihat Akbulut ◽

Gary B. Schuster

Keyword(s):

Diels Alder ◽

Cycloaddition Reactions ◽

Enol Ethers ◽

Ketene Acetals

DFT Study of Thermal 1,3-Dipolar Cycloaddition Reactions between Alkynyl Metal(0) Fischer Carbene Complexes and 3H-1,2-Dithiole-3-thione Derivatives

Organometallics ◽

10.1021/om1007105 ◽

2011 ◽

Vol 30 (3) ◽

pp. 466-476 ◽

Cited By ~ 35

Author(s):

Diego M. Andrada ◽

Alejandro M. Granados ◽

Miquel Solà ◽

Israel Fernández

Keyword(s):

Dft Study ◽

Dipolar Cycloaddition ◽

Cycloaddition Reactions ◽

Fischer Carbene Complexes ◽

Carbene Complexes ◽

Fischer Carbene

ChemInform Abstract: Theoretical Study of the 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides. A DFT Study of Reaction Between Trifluoromethyl Thiomethyl Azomethine Ylide and Acrylonitrile.

ChemInform ◽

10.1002/chin.199934054 ◽

2010 ◽

Vol 30 (34) ◽

pp. no-no

Author(s):

Luis R. Domingo

Keyword(s):

Theoretical Study ◽

Dft Study ◽

Azomethine Ylides ◽

Azomethine Ylide ◽

Dipolar Cycloaddition ◽

Cycloaddition Reactions

A DFT study on the mechanisms for the cycloaddition reactions between 1−aza-2-azoniaallene cations and acetylenes

Journal of Molecular Modeling ◽

10.1007/s00894-012-1521-1 ◽

2012 ◽

Vol 19 (1) ◽

pp. 83-95 ◽

Cited By ~ 3

Author(s):

Jing-mei Wang ◽

Zhi-ming Li ◽

Quan-rui Wang ◽

Feng-gang Tao

Keyword(s):

Dft Study ◽

Cycloaddition Reactions

ChemInform Abstract: MOLECULAR DESIGN BY CYCLOADDITION REACTIONS. PART 43. CYCLOADDITION REACTIONS S OF SILYL ENOL ETHERS OF 2-ACETYLFURAN AND -THIOPHENE AND RELATED BENZO ANALOGS

Chemischer Informationsdienst ◽

10.1002/chin.198444071 ◽

1984 ◽

Vol 15 (44) ◽

Author(s):

T. SASAKI ◽

Y. ISHIBASHI ◽

M. OHNO

Keyword(s):

Molecular Design ◽

Cycloaddition Reactions ◽

Enol Ethers ◽

Silyl Enol Ethers

DFT study on the cycloaddition reactions of [c]-annelated carbo- and heterocyclic five-membered dienes with ethyleneElectronic supplementary information (ESI) available: figures and tables of the principal geometric parameters of all the dienes, transition states and products obtained at the B3LYP/6-31G* level and the Cartesian coordinates of all the optimized structures considered in this study. See http://www.rsc.org/suppdata/p2/b2/b205663a/

Journal of the Chemical Society Perkin Transactions 2 ◽

10.1039/b205663a ◽

2002 ◽

pp. 1902-1908 ◽

Cited By ~ 12

Author(s):

Tandapani C. Dinadayalane ◽

G. Narahari Sastry

Keyword(s):

Transition States ◽

Geometric Parameters ◽

Dft Study ◽

Supplementary Information ◽

Cycloaddition Reactions ◽

Cartesian Coordinates

Halogenocyclopropanation des éthoxy-alcènes diversement alkylés. Effet syn-directeur des groupes éthoxy et alkyles

Canadian Journal of Chemistry ◽

10.1139/v81-090 ◽

1981 ◽

Vol 59 (3) ◽

pp. 621-628 ◽

Cited By ~ 3

Author(s):

Roger Barlet ◽

Raymond Le Goaller ◽

Claude Gey

Keyword(s):

Oxygen Atom ◽

Metal Atom ◽

Cycloaddition Reactions ◽

Enol Ethers ◽

High Yields

Weakly nucleophilic acceptors such as enol ethers can facilitate cycloaddition reactions with monohalocarbenoids. The high yields and stereoselection towards the more highly hindered adducts are interpreted by complexation of the oxygen atom of the substrate with the metal atom of the carbenoid. [Journal translation]

Cycloaddition reactions of acyl ketenes with enol ethers: A general synthesis of 2-alkoxy-2,3-dihydro-4h-pyran-4-ones.

Tetrahedron Letters ◽

10.1016/s0040-4039(00)97442-2 ◽

1990 ◽

Vol 31 (26) ◽

pp. 3677-3680 ◽

Cited By ~ 26

Author(s):

Robert S. Coleman ◽

Eugene B. Grant

Keyword(s):

Cycloaddition Reactions ◽

Enol Ethers ◽

General Synthesis

A DFT study on the mechanisms for the cycloaddition reactions between 1-Aza-2-azoniaallene cations and carbodiimides

International Journal of Quantum Chemistry ◽

10.1002/qua.23065 ◽

2011 ◽

Vol 112 (3) ◽

pp. 809-822 ◽

Cited By ~ 3

Author(s):

Jing-Mei Wang ◽

Zhi-Minhg Li ◽

Quan-Rui Wang ◽

Feng-Gang Tao

Keyword(s):

Dft Study ◽

Cycloaddition Reactions

Electrocatalytic Formal [2+2] Cycloaddition Reactions between Anodically Activated Aliphatic Enol Ethers and Unactivated Olefins Possessing an Alkoxyphenyl Group

ECS Meeting Abstracts ◽

10.1149/ma2009-01/13/617 ◽

2009 ◽

Keyword(s):

Cycloaddition Reactions ◽

Enol Ethers