Russian Chemical Reviews
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive
Impact factor
Guidelines for authors

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Usp. Khim.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Russian Chemical Reviews, 1961, Volume 30, Issue 2, Pages 43–61
DOI: https://doi.org/10.1070/RC1961v030n02ABEH002952
(Mi rcr1622)
 

This article is cited in 10 scientific papers (total in 10 papers)

Stereochemistry of nucleophilic addition reactions to the carbonyl group of cyclic ketones

A. V. Kamernitskii, A. A. Akhrem

N. D. Zelinskii Institute of Organic Chemistry of the USSR Academy of Sciences, Moscow
English full-text Citations (10)
Abstract: CONTENTS
I. Introduction 43
II. Monosubstituted cyclohexanones 43
III. Disubstituted cyclohexanones 47
IV. Trisubstituted cyclohexanones 47
V. Tetrasubstituted cyclohexanones 50
VI. Pentasubstituted cyclohexanones 51
VII. Hexasubstituted cyclohexanones 54
VIII. Attempted generalisation of the results on the stereochemistry of nucleophilic addition to the carbonyl group 55
Russian version:
Uspekhi Khimii, 1961, Volume 30, Issue 2, Pages 142–183
DOI: https://doi.org/10.1070/RC1961v030n02ABEH002952
Document Type: Article
Language: English
Original paper language: Russian


Citation: A. V. Kamernitskii, A. A. Akhrem, “Stereochemistry of nucleophilic addition reactions to the carbonyl group of cyclic ketones”, Usp. Khim., 30:2 (1961), 142–183; Russian Chem. Reviews, 30:2 (1961), 43–61
Linking options:
  • https://www.mathnet.ru/eng/rcr1622
  • https://doi.org/10.1070/RC1961v030n02ABEH002952
  • https://www.mathnet.ru/eng/rcr/v30/i2/p142
  • This publication is cited in the following 10 articles:
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Успехи химии Russian Chemical Reviews
    Statistics & downloads:
    Abstract page:135
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2024