20830352

Source:http://linkedlifedata.com/resource/pubmed/id/20830352

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0175921, umls-concept:C0332514, umls-concept:C1514468, umls-concept:C1880355
pubmed:issue	41
pubmed:dateCreated	2010-10-12
pubmed:abstractText	The process of asymmetric organoautocatalysis appears to be a natural extension to asymmetric organocatalysis, and holds implications for models on the origin of biological homochirality. The discovery of asymmetric organoautocatalysis (i.e. the process in which the chiral product of a purely organic reaction acts as an organocatalyst for its own formation under conservation of its absolute configuration) and more recent reports on related systems are discussed in this review.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Organic Chemicals
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1364-548X
pubmed:author	pubmed-author:TsogoevaSvetlana BSB
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	46
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	7662-9
pubmed:meshHeading	pubmed-meshheading:20830352-Catalysis, pubmed-meshheading:20830352-Organic Chemicals, pubmed-meshheading:20830352-Stereoisomerism, pubmed-meshheading:20830352-Substrate Specificity
pubmed:year	2010
pubmed:articleTitle	When chiral product and catalyst are the same: discovery of asymmetric organoautocatalysis.
pubmed:affiliation	Department of Chemistry and Pharmacy, Chair of Organic Chemistry I, University of Erlangen-Nuremberg, Henkestrasse 42, 91054 Erlangen, Germany. tsogoeva@chemie.uni-erlangen.de
pubmed:publicationType	Journal Article, Review, Research Support, Non-U.S. Gov't