A Modified Synthetic Approach to Optically Pure Benzoxazepines from Amino Acid Precursors Using Intramolecular Buchwald–Hartwig C–O Bond-Formation Reaction
EPrints@IICB
View Archive InfoField | Value | |
Title |
A Modified Synthetic Approach to Optically Pure Benzoxazepines from Amino Acid Precursors Using Intramolecular Buchwald–Hartwig C–O Bond-Formation Reaction
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Creator |
Bhattacharya, Debleena
Behera, Ashok Hota, Sandip K Chattopadhyay, Partha |
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Subject |
Chemistry
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Description |
Palladium-catalyzed intramolecular aryl etherification reaction using bulky binaphthylphosphane ligand is shown to be a convenient method for the synthesis of seven-membered heterocycles. Application of this methodology to a naturally occurring proteinogenic L-amino acid has led to the synthesis of optically active benzoxazepine ring systems of versatile biological importance |
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Date |
2011
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Type |
Article
PeerReviewed |
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Format |
application/pdf
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Identifier |
http://www.eprints.iicb.res.in/83/1/SYNTHESIS%2DSTUTTGART%2C4%2C585%2D592%2C2011[90].pdf
Bhattacharya, Debleena and Behera, Ashok and Hota, Sandip K and Chattopadhyay, Partha (2011) A Modified Synthetic Approach to Optically Pure Benzoxazepines from Amino Acid Precursors Using Intramolecular Buchwald–Hartwig C–O Bond-Formation Reaction. SYNTHESIS (4). pp. 585-592. |
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Relation |
http://dx.doi.org/10.1055/s-0030-1258406
http://www.eprints.iicb.res.in/83/ |
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