A new synthetic approach to tv-protected amino aldehydes
Joint Authors
Hamdan, Abd Allah J.
Ismail, Zaynuhum M.
Source
The Arabian Journal for Science and Engineering
Issue
Vol. 19, Issue 4A (31 Oct. 1994), pp.661-665, 5 p.
Publisher
King Fahd University of Petroleum and Minerals
Publication Date
1994-10-31
Country of Publication
Saudi Arabia
No. of Pages
5
Main Subjects
Abstract EN
N-Protected (Boc- & Z-) L-a-amino acids have been converted to activated mixed anhydrides by reaction either with N,N-dimethylchloroiminium chloride to form (in situ) the imidate or with diethyl phosphorochloridate in the presence of pyridine.
Subsequent reduction of these anhydrides using either DIBAL or lithium tri-/-butoxyaluminum hydride gives the corresponding aldehydes.
Keywords: Organic Chemistry/Amino Acids, Peptides, and Proteins.
American Psychological Association (APA)
Ismail, Zaynuhum M.& Hamdan, Abd Allah J.. 1994. A new synthetic approach to tv-protected amino aldehydes. The Arabian Journal for Science and Engineering،Vol. 19, no. 4A, pp.661-665.
https://search.emarefa.net/detail/BIM-395084
Modern Language Association (MLA)
Ismail, Zaynuhum M.& Hamdan, Abd Allah J.. A new synthetic approach to tv-protected amino aldehydes. The Arabian Journal for Science and Engineering Vol. 19, no. 4A (Oct. 1994), pp.661-665.
https://search.emarefa.net/detail/BIM-395084
American Medical Association (AMA)
Ismail, Zaynuhum M.& Hamdan, Abd Allah J.. A new synthetic approach to tv-protected amino aldehydes. The Arabian Journal for Science and Engineering. 1994. Vol. 19, no. 4A, pp.661-665.
https://search.emarefa.net/detail/BIM-395084
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 665
Record ID
BIM-395084
