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Olivanic acid analogues. Part 10. 1 X-ray crystallographic study of the stereochemistry of some 7-heteroatom-substituted 7-acetyl-8-oxo-3-oxa-1-azabicyclo[4.2.0]octane-2-spirocyclohexanes : functional group control of the stereoselectivity of their reduction products using borohydride reagents
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Published in: | Perkin transactions. 1 1992 (11), p.1305-1312 |
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creator | BATESON, J. H FELL, S. C. M SOUTHGATE, R EGGLESTON, D. S BAURES, P. W |
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Part 10. 1 X-ray crystallographic study of the stereochemistry of some 7-heteroatom-substituted 7-acetyl-8-oxo-3-oxa-1-azabicyclo[4.2.0]octane-2-spirocyclohexanes : functional group control of the stereoselectivity of their reduction products using borohydride reagents</title><source>Royal Society of Chemistry: Jisc Collections: Journals Archive 1841-2007 (2019-2023)</source><creator>BATESON, J. H ; FELL, S. C. M ; SOUTHGATE, R ; EGGLESTON, D. S ; BAURES, P. W</creator><creatorcontrib>BATESON, J. H ; FELL, S. C. M ; SOUTHGATE, R ; EGGLESTON, D. S ; BAURES, P. 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Part 10. 1 X-ray crystallographic study of the stereochemistry of some 7-heteroatom-substituted 7-acetyl-8-oxo-3-oxa-1-azabicyclo[4.2.0]octane-2-spirocyclohexanes : functional group control of the stereoselectivity of their reduction products using borohydride reagents</title><title>Perkin transactions. 1</title><subject>Chemistry</subject><subject>Condensed matter: structure, mechanical and thermal properties</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms</subject><subject>Organic chemistry</subject><subject>Organic compounds</subject><subject>Physics</subject><subject>Preparations and properties</subject><subject>Structure of solids and liquids; crystallography</subject><subject>Structure of specific crystalline solids</subject><issn>0300-922X</issn><issn>2050-8255</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNqNjjtPw0AQhA0CifD4D1sguovONg4JLQLRQUERCaFoc97Yhy5ea_ccYX49RwQFHc0-5puR5jCbFLayZl5U1VE2saW1ZlEUy5PsVPXdWpvbxWxycPUU_A477wCdrwE7DNwMpFN4RomQ2ynksDSCIzgZNWJIXLBvU0LjUI_AG4gtpYeE2LW09RplLytvCW5MSwkxRt4aHdYafRwi1QmgozgGMzf8waZME01u8BPX3o0u8Ov1tJjaN3YROzKF0d4L70lLH0lSuIXN0LnoObWGRnjowXEXhcPfVkqBkm3n429dLyBUD_ss9MLfp8KgvmtgzcLtWIuvKZmwoS7qeXa8waB08bPPssuH-5e7R9OjOgwbwc55XfXityjjqirLxczm5T9tXwtWkGg</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>BATESON, J. 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ispartof | Perkin transactions. 1, 1992 (11), p.1305-1312 |
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source | Royal Society of Chemistry: Jisc Collections: Journals Archive 1841-2007 (2019-2023) |
subjects | Chemistry Condensed matter: structure, mechanical and thermal properties Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms Organic chemistry Organic compounds Physics Preparations and properties Structure of solids and liquids crystallography Structure of specific crystalline solids |
title | Olivanic acid analogues. Part 10. 1 X-ray crystallographic study of the stereochemistry of some 7-heteroatom-substituted 7-acetyl-8-oxo-3-oxa-1-azabicyclo[4.2.0]octane-2-spirocyclohexanes : functional group control of the stereoselectivity of their reduction products using borohydride reagents |
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