Details
| Original language | English |
|---|---|
| Pages (from-to) | 2537-2540 |
| Number of pages | 4 |
| Journal | Journal of the Chemical Society, Perkin Transactions 1 |
| Issue number | 10 |
| Publication status | Published - 1 Dec 1991 |
| Externally published | Yes |
Abstract
A synthesis of [3-13C]- and [3-14C]-3-amino-2- phenylpropionic acids 7a and 7b is described. The incorporation of this amino acid into tenellin 1 from Beauveria bassiana (Bals.) Vuill. and into tropic acid 10 moiety of the tropane alkaloids hyscoyamine 8 and scopolamine 9 from Datura innoxia was studied but proved unsuccessful in each case.
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In: Journal of the Chemical Society, Perkin Transactions 1, No. 10, 01.12.1991, p. 2537-2540.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Synthesis of isotopically labelled 3-amino-2-phenylpropionic acid and its role as a precursor in the biosynthesis of tenellin and tropic acid
AU - Cox, Russell J.
AU - O'Hagan, David
PY - 1991/12/1
Y1 - 1991/12/1
N2 - A synthesis of [3-13C]- and [3-14C]-3-amino-2- phenylpropionic acids 7a and 7b is described. The incorporation of this amino acid into tenellin 1 from Beauveria bassiana (Bals.) Vuill. and into tropic acid 10 moiety of the tropane alkaloids hyscoyamine 8 and scopolamine 9 from Datura innoxia was studied but proved unsuccessful in each case.
AB - A synthesis of [3-13C]- and [3-14C]-3-amino-2- phenylpropionic acids 7a and 7b is described. The incorporation of this amino acid into tenellin 1 from Beauveria bassiana (Bals.) Vuill. and into tropic acid 10 moiety of the tropane alkaloids hyscoyamine 8 and scopolamine 9 from Datura innoxia was studied but proved unsuccessful in each case.
UR - http://www.scopus.com/inward/record.url?scp=37049080638&partnerID=8YFLogxK
U2 - 10.1039/p19910002537
DO - 10.1039/p19910002537
M3 - Article
AN - SCOPUS:37049080638
SP - 2537
EP - 2540
JO - Journal of the Chemical Society, Perkin Transactions 1
JF - Journal of the Chemical Society, Perkin Transactions 1
SN - 1472-7781
IS - 10
ER -