[Quantitative evaluation of Ehrlich's aldehyde reaction after loading].

Z DENES; L EGLER; J HAGEDORN

Home/Archive/PubMed

PubMed · 13721851

[Quantitative evaluation of Ehrlich's aldehyde reaction after loading].

Z DENES·L EGLER·J HAGEDORN

View original source ↗Export metadata ↓

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Aldehydes Liver Function Tests LIVER FUNCTION TESTS Journal Article

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

Z DENES, L EGLER, J HAGEDORN. 1960-12-11. [Quantitative evaluation of Ehrlich's aldehyde reaction after loading].. https://pubmed.ncbi.nlm.nih.gov/13721851/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

PubMed2007

Catalytic enantioselective allenylation reactions of aldehydes with tethered bis(8-quinolinolato) (TBOx) chromium complex.

Explore the source record for details and available documents.

Aldehydes↗

PubMed2007

Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones.

Shuffling of two simple building blocks and a regioselective transfer hydrogenation allow for the rapid synthesis of a small collection of lepidopteran sex pheromones, e.g., 8E,10Z-tetradeca-8,10-dienal 5c, from the horse chestnut leafminer (Cameraria ohridella).

Aldehydes↗

PubMed2007

First enantiospecific total synthesis of the important biogenetic intermediates, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epi-vellosimine and macusine A.

The first enantiospecific total synthesis of the alkaloids 16-epi-vellosimine (1), (+)-polyneuridine (2), (+)-polyneuridine aldehyde (3), and macusine A (4) is reported. The key oxidation was accomplished with the Corey-Kim reagent to provide the important biogenetic intermediates, 16-epi-vellosimine (1) and polyneuridine aldehyde (3), the latter of which is required for the conversion of the sarpagan skeleton into the ajmalan system in the biosynthesis of quebrachidine. [reaction: see text].

Aldehydes↗