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Total Synthesis of a Pyrrolidin‐2‐one with the Structure Proposed for the Alkaloid Rigidiusculamide A
Author(s) -
Radha Krishna Palakodety,
Karunakar Reddy Bonepally
Publication year - 2013
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.201200598
Subject(s) - chemistry , alkaloid , total synthesis , dihydroxylation , stereochemistry , salt metathesis reaction , ring closing metathesis , metathesis , ring (chemistry) , organic chemistry , enantioselective synthesis , polymerization , polymer , catalysis
The total synthesis of the pyrrolidinone alkaloid rigidiusculamide A is reported starting from L ‐tyrosine, using amidation, ring‐closing metathesis, and dihydroxylation as the key reactions.
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