Organic Chemistry Phenomena

"Organic Chemistry Phenomena" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

The conformation, properties, reaction processes, and the properties of the reactions of carbon compounds.

Descriptor ID

D055601

MeSH Number(s)

G02.607

Concept/Terms

Organic Chemistry Phenomena

Below are MeSH descriptors whose meaning is more general than "Organic Chemistry Phenomena".

Biological Sciences [G]
Chemical Phenomena [G02]
Organic Chemistry Phenomena [G02.607]

Below are MeSH descriptors whose meaning is related to "Organic Chemistry Phenomena".

Below are MeSH descriptors whose meaning is more specific than "Organic Chemistry Phenomena".

Organic Chemistry Phenomena
Isomerism
Organic Chemistry Processes

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Organic Chemistry Phenomena" by people in Harvard Catalyst Profiles by year, and whether "Organic Chemistry Phenomena" was a major or minor topic of these publication.

Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 2006 and 2009

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2006	0	1	1
2009	0	1	1

Below are the most recent publications written about "Organic Chemistry Phenomena" by people in Profiles.

Tracking Distinct RNA Populations Using Efficient and Reversible Covalent Chemistry. Mol Cell. 2015 Sep 03; 59(5):858-66.

View in: PubMed
Diastereomerically pure nucleoside-5'-O-(2-thio-4,4-pentamethylene-1,3,2-oxathiaphospholane)s--substrates for synthesis of P-chiral derivatives of nucleoside-5'-O-phosphorothioates. Chirality. 2011 Mar; 23(3):237-44.

View in: PubMed
Total synthesis of (+)-lyconadin A and related compounds via oxidative C-N bond formation. J Am Chem Soc. 2009 Aug 12; 131(31):11187-94.

View in: PubMed
[Reaction of pyridinium and quinolinium salts having the leaving group at the 2- or 4-position with active methylene compounds]. Yakugaku Zasshi. 2006 Feb; 126(2):99-108.

View in: PubMed
Organoastatine chemistry. Astatination via electrophilic destannylation. Int J Rad Appl Instrum A. 1986; 37(8):799-802.

View in: PubMed
Regulation of protein synthesis by phosphorylation of eukaryotic initiation factor 2 alpha in intact reticulocytes and reticulocyte lysates. Proc Natl Acad Sci U S A. 1982 Apr; 79(7):2147-51.

View in: PubMed
Pharmacologically active acetylene compounds. I. Structural modifications of oxotremorine. J Med Chem. 1967 Jul; 10(4):615-20.

View in: PubMed
Synthesis of an antigenic copolymer of angiotensin and succinylated poly-L-lysine. Biochim Biophys Acta. 1967 Apr 11; 133(3):582-4.

View in: PubMed
O-diethyl phosphoryl esters of quaternary and tertiary aminophenols. J Med Chem. 1966 Jul; 9(4):632-3.

View in: PubMed
2-Methyl-3-phenoxycyclopropylamine. J Med Chem. 1966 May; 9(3):440-1.

View in: PubMed

Related Networks

People

Explore

Similar Concepts

Top Journals

J Med Chem
Proc Natl Acad Sci U S A
Yakugaku Zasshi
Mol Cell
J Am Chem Soc
Int J Rad Appl Instrum A
Chirality
Biochim Biophys Acta