Synthesis of highly functionalized phenylalanine derivatives via cross-enyne metathesis reactions
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Title |
Synthesis of highly functionalized phenylalanine derivatives via cross-enyne metathesis reactions
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Creator |
KOTHA, S
HALDER, S BRAHMACHARY, E |
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Subject |
amino-acid derivatives
olefin metathesis amino acids and derivatives metathesis dienes diels-alder reaction |
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Description |
A new method for the synthesis of constrained phenylalanine derivatives is described. In this regard, the simple synthesis of acyclic diene building blocks embodying an alpha-amino acid moiety has been achieved. The diene building blocks have been prepared by cross enyne-metathesis reaction as a key step. The Diels-Alder reaction of the dienes with a dienophile such as dimethyl acetylenedicarboxilate (DMAD) followed by oxidation of the resulting cycloadduct gave highly substituted phenylalanine derivatives. (C) 2002 . .
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Publisher |
PERGAMON-ELSEVIER SCIENCE LTD
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Date |
2011-08-26T21:34:58Z
2011-12-26T12:57:36Z 2011-12-27T05:44:09Z 2011-08-26T21:34:58Z 2011-12-26T12:57:36Z 2011-12-27T05:44:09Z 2002 |
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Type |
Article
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Identifier |
TETRAHEDRON, 58(45), 9203-9208
0040-4020 http://dx.doi.org/10.1016/S0040-4020(02)01178-X http://dspace.library.iitb.ac.in/xmlui/handle/10054/11442 http://hdl.handle.net/10054/11442 |
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Language |
en
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