Journal article

ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE

Abstract:: The potential of D-glucuronolactone as a starting material for the synthesis of polyfunctional amino acids is illustrated by its conversion to 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine. © 1986.

Publication status:: Published

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APA Style

Bashyal, B., Chow, H., & Fleet, G. (1986). ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE. TETRAHEDRON LETTERS, 27(27), 3205–3208.

MLA Style

Bashyal, B., et al. “ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE.” TETRAHEDRON LETTERS, vol. 27, no. 27, 1986, pp. 3205–08.

Chicago Style

Bashyal, B, H Chow, and G Fleet. 1986. “ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM DEUTERIUM-GLUCURONOLACTONE.” TETRAHEDRON LETTERS 27 (27): 3205–8.
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Publisher copy:: 10.1016/S0040-4039(00)84755-3

Authors

+ Bashyal, B More by this author

Role:: Author

+ Chow, H More by this author

Role:: Author

+ Fleet, G More by this author

Role:: Author

Journal:: TETRAHEDRON LETTERS More from this journal
Volume:: 27
Issue:: 27
Pages:: 3205-3208
Publication date:: 1986-01-01
DOI:: 10.1016/S0040-4039(00)84755-3
ISSN:: 0040-4039

Language:: English
Pubs id:: pubs:42553
UUID:: uuid:cec8384a-44d7-40ef-a3ed-a8d9cd47bed8
Local pid:: pubs:42553
Source identifiers:: 42553
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 1986

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

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