Carboxy Alkyl Cysteines

dc.contributor.author	Smith, John Walter
dc.date.accessioned	2009-04-14T22:03:26Z
dc.date.accessioned	2022-10-17T21:07:35Z
dc.date.available	2009-04-14T22:03:26Z
dc.date.available	2022-10-17T21:07:35Z
dc.date.copyright	1969
dc.date.issued	1969
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/22066
dc.description.abstract	A. S-Alkyl substituted cysteines and their sulphoxides (I) Structure These compounds comprise a large number of cysteine derivatives in which the thiol hydrogen is replaced by various aliphatic residues. The basic structure is R - S - CH2-CH.(NH2).COOH where R represents the aliphatic residue, which may range in size from methyl to 2-carboxy-1,1-dimethylethyl. The corresponding sulphoxides of the structurally simpler compound are also known to occur naturally, an example of these being S-methyl-L-cysteine.	en_NZ
dc.format	pdf	en_NZ
dc.language	en_NZ
dc.language.iso	en_NZ
dc.publisher	Te Herenga Waka—Victoria University of Wellington	en_NZ
dc.title	Carboxy Alkyl Cysteines	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ
thesis.degree.name	Master of Science	en_NZ

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