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<rss version="2.0"><channel><title>Scientia Research Library</title><link>http://www.scientiaresearchlibrary.com</link><description>Scientia Research Library make easy to publish research articles or research papers, which is a great opportunity for everyone to fulfill their requirements. Different varieties of journals related to science and technology which are scientifically same can be published here. The Scientia Research  Library  is having an  open - access and peer review policy  to permit  and  understand  use with  required  acceptance  of   the  original . Our   aim is to provide researchers from various diverse fields like engineering, applied chemistry, applied science and research etc., a unique way to give light to their findings.</description><article><ArtTitle>
	THERAPEUTIC EFFICACY OF STEREOISOMERS
</ArtTitle><PubName>Scientia Research Library</PubName><JournalName>Journal of Applied Chemistry</JournalName><EISSN>2348 - 0408</EISSN><year>2016</year><volume>4</volume><issue>6</issue><AuthorName>
	*S.S.Agrawal, Tanya Kumar1 and Mohd Mazhar2
	Page No. 1-6
</AuthorName><PageNo>1</PageNo><Abstract>
	Stereoisomers are molecules that are identical in atomic constitution and bonding, but differ in the
	three-dimensional arrangement of the atoms. They are often readily distinguished by biological
	systems, however, and may have different pharmacokinetic properties (absorption; distribution,
	biotransformation. and excretion) and quantitatively or qualitatively different pharmacologic or
	toxicologic effects.Approximately 50% of marketed drugs are chiral having enantiomers and
	approximately 50% of these are mixtures of enantiomers rather than single enantiomers. One
	member of the pair may show inactivity or toxicty compared to the other one. E.g. granulocytopenia
	is related to the d-isomer of levodopa; Vomiting is caused by the d-isomer of levamisole; and
	myasthenia gravis symptoms were no longer observed when the d-isomer was removed from
	d,lcarnitine) etc.[1]This review article emphasis on the application of optical isomers in medical
	researchon issues relating to the study and pharmaceutical activityof individual enantiomers and
	racemates.
	Key Words: Enantiomer, optical isomer,pharmokinetic properties,arrangement of atoms.
</Abstract><URLs><abstract>http://www.scientiaresearchlibrary.com/archive-abs.php?arc=487</abstract><Fulltext><pdf>http://www.scientiaresearchlibrary.com/archive/JAC-2016-4-6-073-1-6.pdf</pdf></Fulltext></URLs></article><article><ArtTitle>
	A Simple and convenient one pot synthesis of aminoquinone derivatives via
	Electrochemical amination of benzoquinone with secondary amines
</ArtTitle><PubName>Scientia Research Library</PubName><JournalName>Journal of Applied Chemistry</JournalName><EISSN>2348 - 0408</EISSN><year>2016</year><volume>4</volume><issue>6</issue><AuthorName>
	Jyoti Malviya1, Shashi Kala2, Hemlata Singh3, R.K.P.Singh*
	Page No. 7-16
</AuthorName><PageNo>1</PageNo><Abstract>
	A simple and efficient method for the convenient synthesis of aminoquinones have been described
	on reaction with catechol and various secondary amines using lithium perchlorate as a supporting
	electrolyte in acetonitrile media at platinum electrode under constant potential electrolysis. The
	results revealed that the o-benzoquinone derived from the oxidation of catechol, participates in
	Michael addition reaction with secondary amines and convert it into the aminoquinones in a good
	yield with high purity.The method is cost-effective, high-yielding, clean, and selective. The products
	of electrosynthesis have been purified and characterized by FTIR, 1HNMR, 13CNMR and
	mechanism was deduced with cyclic voltammetric study.
	Key Words: Anodic oxidation, cyclic voltammetry, electrochemical synthesis, o-benzoquinone
	secondary amines.
</Abstract><URLs><abstract>http://www.scientiaresearchlibrary.com/archive-abs.php?arc=488</abstract><Fulltext><pdf>http://www.scientiaresearchlibrary.com/archive/JAC-2016-4-6-074-7-16.pdf</pdf></Fulltext></URLs></article></channel></rss>
