Journal article

Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives

Abstract:: Regioselective Dieckmann cyclisations using an N-acyloxazolidine derived from L-serine give substituted tetramic acids in high yield and enantioselectivity. The products are easily deprotected under mild conditions to give hydroxymethyltetramic acids.

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.
Cite

Cite this record

APA Style

Andrews, M. D., Brewster, A., Crapnell, K., Ibbett, A., Jones, T., Moloney, M., Prout, K., & Watkin, D. (1998). Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2, 223–235.

MLA Style

Andrews, M. D., et al. “Regioselective Dieckmann Cyclisations Leading to Enantiopure Highly Functionalised Tetramic Acid Derivatives.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 2, 1998, pp. 223–35.

Chicago Style

Andrews, MD, A Brewster, K Crapnell, A Ibbett, T Jones, M Moloney, K Prout, and D Watkin. 1998. “Regioselective Dieckmann Cyclisations Leading to Enantiopure Highly Functionalised Tetramic Acid Derivatives.” JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no. 2: 223–35.
Share
Print

Access Document

Publisher copy:: 10.1039/a706014i

Authors

+ Andrews, MD More by this author

Role:: Author

+ Brewster, A More by this author

Role:: Author

+ Crapnell, K More by this author

Role:: Author

+ Ibbett, A More by this author

Role:: Author

+ Jones, T More by this author

Role:: Author

More authors...

Journal:: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 More from this journal
Issue:: 2
Pages:: 223-235
Publication date:: 1998-01-21
DOI:: 10.1039/a706014i
EISSN:: 1364-5463
ISSN:: 0300-922X

Language:: English
Pubs id:: pubs:36311
UUID:: uuid:3f5a6f9a-f401-4af8-8e31-03208c041f0a
Local pid:: pubs:36311
Source identifiers:: 36311
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1998

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