Diastereoselective reductive N-alkylation of (R,R)-trans-1,2-diaminocyclohexane with prochiral ketones using the Ti(O < sup > i < /sup > Pr) < inf > 4 < /inf > /NaBH < inf > 4 < /inf > system

dc.contributor.author Dalai, Manasi
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:07:50Z
dc.date.available 2022-03-27T09:07:50Z
dc.date.issued 2009-06-19
dc.description.abstract A simple and convenient one-pot method for the reductive N-alkylation of (R,R)-trans-1,2-diaminocyclohexane by prochiral ketones using a Ti(OiPr)4/NaBH4 system to obtain the corresponding alkyl amine derivatives in 76-95% yields with good diastereoselectivity (dr = up to 23:1:1) is reported. © 2009 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Asymmetry. v.20(11)
dc.identifier.issn 09574166
dc.identifier.uri 10.1016/j.tetasy.2009.05.004
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0957416609003632
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12463
dc.title Diastereoselective reductive N-alkylation of (R,R)-trans-1,2-diaminocyclohexane with prochiral ketones using the Ti(O < sup > i < /sup > Pr) < inf > 4 < /inf > /NaBH < inf > 4 < /inf > system
dc.type Journal. Article
dspace.entity.type
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description: