Structural Diversity Based on Cyclopropane Scaffolds
A practical and efficient route for the stereoselective conversion of easily accessible homoallylic alcohols to diastereomerically pure cis- and trans-disubstituted and 1,2,3-trisubstituted cyclopropanes has been developed. The diversity of structures that can be prepared and the simplicity of the o...
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| Veröffentlicht in: | Organic letters 2000-03, Vol.2 (5), p.601-603 |
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| container_title | Organic letters |
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| creator | Taylor, Richard E Schmitt, Michael J Yuan, Haiqing |
| description | A practical and efficient route for the stereoselective conversion of easily accessible homoallylic alcohols to diastereomerically pure cis- and trans-disubstituted and 1,2,3-trisubstituted cyclopropanes has been developed. The diversity of structures that can be prepared and the simplicity of the overall sequence make this route ideal for extension to solid-phase synthesis techniques and ultimately combinatorial library generation. |
| doi_str_mv | 10.1021/ol9913542 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1523-7060 |
| ispartof | Organic letters, 2000-03, Vol.2 (5), p.601-603 |
| issn | 1523-7060 1523-7052 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1859326930 |
| source | ACS Publications |
| title | Structural Diversity Based on Cyclopropane Scaffolds |
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