Journal article

ASYMMETRIC-SYNTHESIS OF THE N-TERMINAL COMPONENT OF MICROGININ - (2S,3R)-3-AMINO-2-HYDROXYDECANOIC ACID, ITS (2R,3R)-EPIMER AND (3R)-3-AMINODECANOIC ACID

Abstract:: 3-Amino-2-hydroxydecanoic acid (AHDA) is a novel amino acid which has been suggested as the N-terminal component of the recently isolated angiotensin-converting enzyme inhibitor microginin. The naturally occurring amino acid was found to possess syn relative stereochemistry and (2S,3R) absolute stereochemistry when the reported 1H and 13C nmr spectroscopic data and the CD data were compared to the spectroscopic data for synthetic (2R,3R)- and (2S,3R)-AHDA. These studies complete the stereochemical assignment of microginin. © 1994.

Publication status:: Published

Actions

Email

Email this record

Send the bibliographic details of this record to your email address.

Your Email
Please enter the email address that the record information will be sent to.

-
Your message (optional)
Please add any additional information to be included within the email.
Share
Cite

Cite this record

APA Style

Bunnage, M., Burke, A., Davies, S., & Goodwin, C. (1995). ASYMMETRIC-SYNTHESIS OF THE N-TERMINAL COMPONENT OF MICROGININ - (2S,3R)-3-AMINO-2-HYDROXYDECANOIC ACID, ITS (2R,3R)-EPIMER AND (3R)-3-AMINODECANOIC ACID. TETRAHEDRON-ASYMMETRY, 6(1), 165–176.

MLA Style

Bunnage, M, et al. “ASYMMETRIC-SYNTHESIS OF THE N-TERMINAL COMPONENT OF MICROGININ - (2S,3R)-3-AMINO-2-HYDROXYDECANOIC ACID, ITS (2R,3R)-EPIMER AND (3R)-3-AMINODECANOIC ACID.” TETRAHEDRON-ASYMMETRY, vol. 6, no. 1, 1995, pp. 165–76.

Chicago Style

Bunnage, M, A Burke, S Davies, and C Goodwin. 1995. “ASYMMETRIC-SYNTHESIS OF THE N-TERMINAL COMPONENT OF MICROGININ - (2S,3R)-3-AMINO-2-HYDROXYDECANOIC ACID, ITS (2R,3R)-EPIMER AND (3R)-3-AMINODECANOIC ACID.” TETRAHEDRON-ASYMMETRY 6 (1): 165–76.
Print

Access Document

Publisher copy:: 10.1016/0957-4166(94)00372-I

Authors

+ Bunnage, M More by this author

Role:: Author

+ Burke, A More by this author

Role:: Author

+ Davies, S More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Goodwin, C More by this author

Role:: Author

Journal:: TETRAHEDRON-ASYMMETRY More from this journal
Volume:: 6
Issue:: 1
Pages:: 165-176
Publication date:: 1995-01-01
DOI:: 10.1016/0957-4166(94)00372-I
EISSN:: 1362-511X
ISSN:: 0957-4166

Pubs id:: pubs:110856
UUID:: uuid:15a3c645-9001-4939-b0a9-872e512a68b6
Local pid:: pubs:110856
Source identifiers:: 110856
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_15a3c64590014939b0a9872e512a68b6

Terms of use

Copyright date:: 1995

Licence:: Terms and Conditions of Use for Oxford University Research Archive

Views and Downloads

About views and downloads

If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP