Literature DB >> 5357020

Acid-catalysed dehydration of dehydroretinol.

P G Nayar.   

Abstract

1. Treatment of dehydroretinol with hydrogen chloride in light petroleum or toluene-p-sulphonic acid in benzene produces a substance with u.v.-absorption maxima at 284, 296, 310, 350, 368, 388, 408 and 433nm. and antimony trichloride colour maximum at 620nm. This compound is tentatively named compound 433 after its absorption maximum at 433nm. 2. Treatment of dehydroretinol with ethanolic hydrogen chloride produces, besides 3-ethoxyanhydroretinol, some compound 433 also. 3. Compound 433 is present in several freshwater-fish liver oils. 4. The i.r. spectrum of compound 433 shows only a band attributable to a conjugated ethylenic system. 5. The course of changes that lead to the formation of compound 433 is discussed.

Entities:  

Mesh:

Substances:

Year:  1969        PMID: 5357020      PMCID: PMC1185204          DOI: 10.1042/bj1150765

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  4 in total

1.  Anhydrovitamin A2 and rehydrovitamin A2.

Authors:  S BALASUNDARAM; M S BAMJI; H R CAMA; T N VARMA; P R SUNDARESAN
Journal:  J Biol Chem       Date:  1958-10       Impact factor: 5.157

2.  Absorption spectra of substances derived from vitamin A.

Authors:  J R Edisbury; A E Gillam; I M Heilbron; R A Morton
Journal:  Biochem J       Date:  1932       Impact factor: 3.857

3.  Isolation of Pure Vitamin A2.

Authors:  E M Shantz
Journal:  Science       Date:  1948-10-15       Impact factor: 47.728

4.  Naturally occurring anhydrovitamin A2. Transformation into retinene.

Authors:  R K Barua; P G Nayar
Journal:  Biochem J       Date:  1966-11       Impact factor: 3.857

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.