Home / Articles / β-Ketovinylation

β-Ketovinylation

Margarita Iosifovna Rybinskaya 1
Margarita Iosifovna Rybinskaya
, 
Aleksandr Nikolaevich Nesmeyanov 1
Aleksandr Nikolaevich Nesmeyanov
, 
Nikolai Konstantinovich Kochetkov 2
Nikolai Konstantinovich Kochetkov
1 A. N. Nesmeyanov Institute of Organoelement Compounds, USSR Academy of Sciences, Moscow
2 N. D. Zelinskii Institute of Organic Chemistry of the USSR Academy of Sciences, Moscow
Published 30 November 1968
Communication , Volume 38, Issue 6, 433-455
46
Share
Cite this
GOST
 | 
Cite this
GOST
Rybinskaya M. I., Nesmeyanov A. N., Kochetkov N. K. β-Ketovinylation // Russian Chemical Reviews. 1969. Vol. 38. No. 6. pp. 433-455.
GOST all authors (up to 50)
Rybinskaya M. I., Nesmeyanov A. N., Kochetkov N. K. β-Ketovinylation // Russian Chemical Reviews. 1969. Vol. 38. No. 6. pp. 433-455.
RIS
 | 
Cite this
RIS
TY - JOUR
DO - 10.1070/RC1969v038n06ABEH001752
UR - https://rcr.colab.ws/publications/10.1070/RC1969v038n06ABEH001752
TI - β-Ketovinylation
T2 - Russian Chemical Reviews
AU - Rybinskaya, Margarita Iosifovna
AU - Nesmeyanov, Aleksandr Nikolaevich
AU - Kochetkov, Nikolai Konstantinovich
PY - 1969
DA - 1968/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 433-455
IS - 6
VL - 38
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors)
@article{1969_Rybinskaya,
author = {Margarita Iosifovna Rybinskaya and Aleksandr Nikolaevich Nesmeyanov and Nikolai Konstantinovich Kochetkov},
title = {β-Ketovinylation},
journal = {Russian Chemical Reviews},
year = {1969},
volume = {38},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1969v038n06ABEH001752},
number = {6},
pages = {433--455},
doi = {10.1070/RC1969v038n06ABEH001752}
}
MLA
Cite this
MLA
Rybinskaya, Margarita Iosifovna, et al. “β-Ketovinylation.” Russian Chemical Reviews, vol. 38, no. 6, Nov. 1969, pp. 433-455. https://rcr.colab.ws/publications/10.1070/RC1969v038n06ABEH001752.
Views / Visits / Downloads
21 / 21 / 10

Abstract

The review deals with the methods of introduction into the molecule of the group RCOCR'=CR'', which has come to be called the β-ketovinylation reaction. It has been shown that the principal starting materials for these reactions are certain β-substituted vinyl ketones, which have surpassed all other activated ethylene compounds in their importance for synthetic organic chemistry. A systematic description of literature data has been given in accordance with methods for C-, N-, O-, S-, P-, Hal-, Fe-, and Co-ketovinylation. This made it possible to make generalisations and recommendations concerning the choice of the ketovinylating agent in particular cases. The possible mechanism of β-ketovinylation is discussed, particular attention being devoted to kinetic and stereochemical data. The bibliography comprises 300 references.