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Synthesis of excitatory amino acid analogues

Abstract:
A general route to excitatory amino acid analogues has been developed as exemplified by the synthesis of A-1 and A-2. The key reactions involved were a Negishi coupling of Jackson's organozinc reagent with vinyl bromide 8 and subsequent ring closure of 15 and 16 using the Mitsunobu reaction. © Georg Thieme Verlag Stuttgart.
Publication status:
Published

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Publisher copy:
10.1055/s-2006-950399

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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Role:
Author
Journal:
SYNLETT
Volume:
2006
Issue:
15
Pages:
2407-2410
Publication date:
2006-09-18
DOI:
EISSN:
1437-2096
ISSN:
0936-5214
URN:
uuid:908e3018-2488-47f2-84e6-7056f87f24d4
Source identifiers:
118263
Local pid:
pubs:118263

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