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Regioselective Synthesis of Chiral Six- and Seven-Membered N-Heterocycles from N-AIIyl Carbohydrate Nitrones: Tuning of Regioselectivity by N-Substitution
EPrints@IICB
View Archive Info| Field | Value | |
| Title |
Regioselective Synthesis of Chiral Six- and Seven-Membered N-Heterocycles from N-AIIyl Carbohydrate Nitrones: Tuning of Regioselectivity by N-Substitution |
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| Creator |
Majmndar, Swapan
Bhattacharjya, Anup Patra, Amarendra |
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| Subject |
Chemistry
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| Description |
The intramoleodar cydoaddition of N-allyl carbohydrate nitrones leads to enantiomefically pure six- and seven-membered nitrogen heterocydes and the regioselectivity of the cycloaddition was controlled by changing the substituent on the nitrogea atom of the N-allyl moiety. © 1999 Elsevier Science Ltd. All rights reserved |
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| Publisher |
Elsevier
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| Date |
1999
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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/731/1/TETRAHEDRON__55_(41)12157%2D12174;1999[15].pdf
Majmndar, Swapan and Bhattacharjya, Anup and Patra, Amarendra (1999) Regioselective Synthesis of Chiral Six- and Seven-Membered N-Heterocycles from N-AIIyl Carbohydrate Nitrones: Tuning of Regioselectivity by N-Substitution. Tetrahedron, 55 (41). pp. 12157-12174. |
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| Relation |
http://dx.doi.org/10.1016/S0040-4020(99)00694-8
http://www.eprints.iicb.res.in/731/ |
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