π-facial selectivities of diastereotopic ketones: P-bromobenzoates of 4-hetero-1-decalinols

dc.contributor.author Parvez, M.
dc.contributor.author Yadav, V. K.
dc.contributor.author Balamurugan, R.
dc.date.accessioned 2022-03-27T08:39:47Z
dc.date.available 2022-03-27T08:39:47Z
dc.date.issued 2001-01-01
dc.description.abstract The crystal structures of the p-bromobenzoates of cis-4-oxa-1-decalinyl (C16H19BrO3), trans-4-oxa-1-decalinyl (C16H19BrO3), N-benzyl-cis-4-aza-1-decalinyl (C23H26BrNO2), N-benzyl-trans-4-aza-1-decalinyl (C23H26BrNO2) and trans-4-thia-1-decalinyl (C16H19BrO2S) (decalin is perhydronaphthalene) have been determined as part of a study directed at predicting and interpreting the π-facial selectivities of diastereotopic ketones in reactions with nucleophiles. All five structures are composed of molecules that are separated by normal van der Waals distances. In all five structures, the heterocyclic and cyclohexyl rings adopt chair conformations, and the p-bromobenzoate groups are planar.
dc.identifier.citation Acta Crystallographica Section C: Crystal Structure Communications. v.57(9)
dc.identifier.issn 01082701
dc.identifier.uri 10.1107/S0108270101009544
dc.identifier.uri http://scripts.iucr.org/cgi-bin/paper?S0108270101009544
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11410
dc.title π-facial selectivities of diastereotopic ketones: P-bromobenzoates of 4-hetero-1-decalinols
dc.type Journal. Article
dspace.entity.type
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