Synthesis of novel 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives through the application of rongalite: A synergistic combination of [2+2+2]- and [4+2]-cycloaddition reactions
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Title |
Synthesis of novel 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives through the application of rongalite: A synergistic combination of [2+2+2]- and [4+2]-cycloaddition reactions
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Creator |
KOTHA, S
BANERJEE, S |
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Subject |
phenylethanolamine n-methyltransferase
diversity-oriented synthesis natural-product hybrids asymmetric-synthesis amino-acids napieralski reaction constrained analogs peptide antagonists tic derivatives potent 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid rongalite cycloaddition amino acids quinones |
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Description |
An efficient route for the synthesis of several novel 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives has been reported. A synergistic combination of [2+2+2]- and [4+2]-cycloaddition reactions has been used for the synthesis of the desired targets.
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Publisher |
GEORG THIEME VERLAG KG
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Date |
2011-07-30T09:18:17Z
2011-12-26T12:52:46Z 2011-12-27T05:39:38Z 2011-07-30T09:18:17Z 2011-12-26T12:52:46Z 2011-12-27T05:39:38Z 2007 |
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Type |
Article
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Identifier |
SYNTHESIS-STUTTGART, (7), 1015-1020
0039-7881 http://dx.doi.org/10.1055/s-2007-965946 http://dspace.library.iitb.ac.in/xmlui/handle/10054/7915 http://hdl.handle.net/10054/7915 |
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Language |
en
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