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Can I read Enantioselective synthesis of protected d-serine from tetrahydrooxazin-4-one via a hetero Diels–Alder reaction on EtoBox?

Enantioselective synthesis of protected d-serine from tetrahydrooxazin-4-one via a hetero Diels–Alder reaction by Mauro Panunzio; Elisa Bandini; Eileen Campana; Paola Vicennati is a Chemistry article available to read on EtoBox.

What is Enantioselective synthesis of protected d-serine from tetrahydrooxazin-4-one via a hetero Diels–Alder reaction about?

Hetero Diels-Alder reaction between 2-aza-3-trimethylsilyloxy-1,3-diene and aldehydes gives rise to tetrahydrooxazin-4ones, useful intermediates in the synthesis of a-amino-b-hydroxy acids. Herein we report the complete stereoselective synthesis of D-serine Cbz-methyl ester.

Who reads Enantioselective synthesis of protected d-serine from tetrahydrooxazin-4-one via a hetero Diels–Alder reaction?

It is typically read by researchers, students, and practitioners in Chemistry.

Author
Mauro Panunzio; Elisa Bandini; Eileen Campana; Paola Vicennati
Publisher
Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0957-4166)
Published
2002
Language
EN
Field
Chemistry (Physical Sciences)

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