Studies in vilsmeier chemistry, V. Vilsmeier reactions of 2‐alkyl‐2‐cyclohexen‐1‐ones: A novel route to dihydrobenzaldehydes, the formation of allyl alcohols as by‐products, and the X‐ray crystallographic structure of 3‐chloro‐2‐methyl‐2‐cyclohexen‐1‐ol-Reference-Cited by-同舟云学术

Studies in vilsmeier chemistry, V. Vilsmeier reactions of 2‐alkyl‐2‐cyclohexen‐1‐ones: A novel route to dihydrobenzaldehydes, the formation of allyl alcohols as by‐products, and the X‐ray crystallographic structure of 3‐chloro‐2‐methyl‐2‐cyclohexen‐1‐ol

Published:1988-05 Issue:5 Volume:121 Page:999-1003
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Katritzky Alan R.¹,Wang Zuoquan¹,Marson Charles M.¹,Offerman Rick J.¹,Koziol Anna E.¹,Palenik Gus J.¹

Affiliation:

1. Department of Chemistry, University of Florida, Gainesville, FL 32611

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19881210526

Reference25 articles.

1. A stable 3-methylene-1,4-cyclohexadiene: a non-aromatic tautomer of a simple benzene

2. Reactions of 2-cyclohexen-1-ones and cyclohexane-1,3-diones with chloro methylene iminium salts

3. Reactions of alkyl-substituted 2-cyclohexen-1-ones with Vilsmeier reagents

4. (1d) –A. R.Katritzky C. M.Marson G. J.Palenik A. E.Koziol H.Luce M.Karelson B.‐C.Chen W.Brey Tetrahedron in press.

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