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3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone
The title bicyclic lactone, C(19)H(19)NO(3), is an intermediate in the synthesis of chiral α-methylprolines and branched C-methyl pyrrolidines; the absolute configuration was determined by the use of d-erythronolactone as the starting material. It exhibits no unusual crystal packing features, and...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2008
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959362/ https://www.ncbi.nlm.nih.gov/pubmed/21201113 http://dx.doi.org/10.1107/S1600536808027888 |
| _version_ | 1782188481328447488 |
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| author | da Cruz, Filipa P. Booth, K. Victoria Fleet, George W. J. Watkin, David J. |
| author_facet | da Cruz, Filipa P. Booth, K. Victoria Fleet, George W. J. Watkin, David J. |
| author_sort | da Cruz, Filipa P. |
| collection | PubMed |
| description | The title bicyclic lactone, C(19)H(19)NO(3), is an intermediate in the synthesis of chiral α-methylprolines and branched C-methyl pyrrolidines; the absolute configuration was determined by the use of d-erythronolactone as the starting material. It exhibits no unusual crystal packing features, and each molecule acts as a donor and acceptor for one C—H⋯O hydrogen bond. |
| format | Text |
| id | pubmed-2959362 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2008 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29593622010-12-30 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone da Cruz, Filipa P. Booth, K. Victoria Fleet, George W. J. Watkin, David J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title bicyclic lactone, C(19)H(19)NO(3), is an intermediate in the synthesis of chiral α-methylprolines and branched C-methyl pyrrolidines; the absolute configuration was determined by the use of d-erythronolactone as the starting material. It exhibits no unusual crystal packing features, and each molecule acts as a donor and acceptor for one C—H⋯O hydrogen bond. International Union of Crystallography 2008-09-06 /pmc/articles/PMC2959362/ /pubmed/21201113 http://dx.doi.org/10.1107/S1600536808027888 Text en © Cruz et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
| spellingShingle | Organic Papers da Cruz, Filipa P. Booth, K. Victoria Fleet, George W. J. Watkin, David J. 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone |
| title | 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone |
| title_full | 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone |
| title_fullStr | 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone |
| title_full_unstemmed | 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone |
| title_short | 3-O-Benzhydryl-2,5-dideoxy-2,5-imino-2-C-methyl-l-lyxono-1,4-lactone |
| title_sort | 3-o-benzhydryl-2,5-dideoxy-2,5-imino-2-c-methyl-l-lyxono-1,4-lactone |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959362/ https://www.ncbi.nlm.nih.gov/pubmed/21201113 http://dx.doi.org/10.1107/S1600536808027888 |
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