Diastereoselective strategies for the synthesis of glutamate-containing natural products: Total synthesis of (S)-(+)-lycoperdic acid and studies toward the total synthesis of (-)-dysiherbaine and the design and synthesis of a scaffold for glutamate receptor ligands using a natural product-based library approach

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" Diastereoselective strategies for the synthesis of glutamate-containing natural products: Total synthesis of (S)-(+)-lycoperdic acid and studies toward the total synthesis of (-)-dysiherbaine and the design and synthesis of a scaffold for glutamate receptor ligands using a natural product-based library approach "

Record identifier	:	566022
Personal Name - Primary Intelectual Responsibility	:	Cohen, Jamie Lisa
Title and statement of responsibility	:	Diastereoselective strategies for the synthesis of glutamate-containing natural products: Total synthesis of (S)-(+)-lycoperdic acid and studies toward the total synthesis of (-)-dysiherbaine and the design and synthesis of a scaffold for glutamate receptor ligands using a natural product-based library approach [Thesis]
Publication, Distribution,Etc.	:	University of California, Irvine, 2006
Language of Text,Soundtrack etc.	:	eng
Dissertation of thesis details and type of degree	:	phd
Body granting the degree	:	, University of California, Irvine
Summary or Abstract	:	Chapter 1 of this dissertation reviews the recent use of pyroglutamic acid as a chiral building block for asymmetric natural product synthesis. The synthetic examples illustrated in this chapter provide a foundation for the research projects described in the remainder of this dissertation, which investigate the diastereoselective reactions of pyroglutamic acid derivatives for the synthesis of glutamate-containing natural products and analogs..
Topical Name Used as Subject	:	Organic chemistry
Information of biblio record	:	TL
Material Type	:	Latin Dissertation

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