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Total synthesis of antifungal gamahonolide A
[Display omitted] The first stereoselective total synthesis of gamahonolide A (1) has been accomplished using aminoxylation, Keck allylation, and ring-closing metathesis (RCM) reactions as key steps.
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| Published in: | Tetrahedron letters 2014-05, Vol.55 (21), p.3227-3228 |
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| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c372t-634e22696b3da893c1f02c9775d3ff2bd2f13aba5bbcd7b6a3a4738628bd6ed93 |
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| cites | cdi_FETCH-LOGICAL-c372t-634e22696b3da893c1f02c9775d3ff2bd2f13aba5bbcd7b6a3a4738628bd6ed93 |
| container_end_page | 3228 |
| container_issue | 21 |
| container_start_page | 3227 |
| container_title | Tetrahedron letters |
| container_volume | 55 |
| creator | Sabitha, Gowravaram Reddy, K. Purushotham Reddy, S. Purushotham Yadav, J.S. |
| description | [Display omitted]
The first stereoselective total synthesis of gamahonolide A (1) has been accomplished using aminoxylation, Keck allylation, and ring-closing metathesis (RCM) reactions as key steps. |
| doi_str_mv | 10.1016/j.tetlet.2014.04.026 |
| format | article |
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The first stereoselective total synthesis of gamahonolide A (1) has been accomplished using aminoxylation, Keck allylation, and ring-closing metathesis (RCM) reactions as key steps.</description><subject>Allyl compounds</subject><subject>Aminoxylation</subject><subject>Antifungal</subject><subject>Chemical reactions</subject><subject>Decomposition reactions</subject><subject>Keck allylation</subject><subject>Metathesis</subject><subject>Natural product</subject><subject>RCM</subject><subject>Ring-closing metathesis</subject><subject>Synthesis (chemistry)</subject><subject>Tetrahedrons</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFUEtLAzEYDKJgrf4DD3v04K5fHpvNXoRSfEHBSz2HbB5tynZTN6ngvzdlPevHwAfDzMAMQrcYKgyYP-yqZFNvU0UAswoyCD9DMywaWtJa4HM0A2BQMqDtJbqKcQf5uIAZul-HpPoifg9pa6OPRXCFGpJ3x2GT-Y3aq20YQu-NLRbX6MKpPtqb3z9HH89P6-VruXp_eVsuVqWmDUklp8wSwlveUaNESzV2QHTbNLWhzpHOEIep6lTdddo0HVdUsYYKTkRnuDUtnaO7Kfcwhs-jjUnufdS279VgwzFK3DDGBQcQ_0trxgBorp-lbJLqMcQ4WicPo9-r8VtikKcd5U5OO8rTjhIyCM-2x8lmc-Mvb0cZtbeDtsaPVidpgv874Ae8a3yr</recordid><startdate>20140521</startdate><enddate>20140521</enddate><creator>Sabitha, Gowravaram</creator><creator>Reddy, K. Purushotham</creator><creator>Reddy, S. Purushotham</creator><creator>Yadav, J.S.</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20140521</creationdate><title>Total synthesis of antifungal gamahonolide A</title><author>Sabitha, Gowravaram ; Reddy, K. Purushotham ; Reddy, S. Purushotham ; Yadav, J.S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-634e22696b3da893c1f02c9775d3ff2bd2f13aba5bbcd7b6a3a4738628bd6ed93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Allyl compounds</topic><topic>Aminoxylation</topic><topic>Antifungal</topic><topic>Chemical reactions</topic><topic>Decomposition reactions</topic><topic>Keck allylation</topic><topic>Metathesis</topic><topic>Natural product</topic><topic>RCM</topic><topic>Ring-closing metathesis</topic><topic>Synthesis (chemistry)</topic><topic>Tetrahedrons</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sabitha, Gowravaram</creatorcontrib><creatorcontrib>Reddy, K. Purushotham</creatorcontrib><creatorcontrib>Reddy, S. Purushotham</creatorcontrib><creatorcontrib>Yadav, J.S.</creatorcontrib><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sabitha, Gowravaram</au><au>Reddy, K. Purushotham</au><au>Reddy, S. Purushotham</au><au>Yadav, J.S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Total synthesis of antifungal gamahonolide A</atitle><jtitle>Tetrahedron letters</jtitle><date>2014-05-21</date><risdate>2014</risdate><volume>55</volume><issue>21</issue><spage>3227</spage><epage>3228</epage><pages>3227-3228</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>[Display omitted]
The first stereoselective total synthesis of gamahonolide A (1) has been accomplished using aminoxylation, Keck allylation, and ring-closing metathesis (RCM) reactions as key steps.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.tetlet.2014.04.026</doi><tpages>2</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0040-4039 |
| ispartof | Tetrahedron letters, 2014-05, Vol.55 (21), p.3227-3228 |
| issn | 0040-4039 1873-3581 |
| language | eng |
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| source | ScienceDirect Freedom Collection 2022-2024 |
| subjects | Allyl compounds Aminoxylation Antifungal Chemical reactions Decomposition reactions Keck allylation Metathesis Natural product RCM Ring-closing metathesis Synthesis (chemistry) Tetrahedrons |
| title | Total synthesis of antifungal gamahonolide A |
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