Literature summary extracted from

Turner, N.J.; Winterman, J.R.; McCague, R.; Parratt, J.S.; Taylor, S.J.C.
Synthesis of homochiral L-(S)-tert-leucine via a lipase catalysed dynamic resolution process (1995), Tetrahedron Lett., 36 (7), 1113-1116.

No PubMed abstract available

Application

EC Number	Application	Comment	Organism
3.1.1.3	synthesis	production of (S)-ester amide, which is useful as a lipophilic, hindered component of peptides. The amino acids are also useful building blocks for a number of chiral auxiliaries and ligands	Rhizomucor miehei

Organism

EC Number	Organism	UniProt	Comment	Textmining
3.1.1.3	Rhizomucor miehei	-	-	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
3.1.1.3	(4S)-4-tert-butyl-2-phenyl-1,3-oxazol-5(4H)-one + butanol	-	Rhizomucor miehei	butyl (2S)-2-(benzoylamino)3,3-dimethylbutanoate	-	?

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Release 2023.1 (January 2023)