Stereochemistry of Tropine and pseudo-Tropine
ACYL migration N → O was used for the determination of the configuration of the diastereomeric 1.2-amino-alcohols, for example, ephedrine 1 , chloromycetin 2 , as well as for that of the alicyclic amino-alcohols (2-amino- cyclo hexanol and pentanols) containing flexible 3 a or rigid 3 b ring systems...
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| Veröffentlicht in: | Nature (London) 1952-03, Vol.169 (4298), p.462-463 |
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| container_issue | 4298 |
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| container_title | Nature (London) |
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| creator | FODOR, G NÁDOR, K |
| description | ACYL migration N → O was used for the determination of the configuration of the diastereomeric 1.2-amino-alcohols, for example, ephedrine
1
, chloromycetin
2
, as well as for that of the alicyclic amino-alcohols (2-amino-
cyclo
hexanol and pentanols) containing flexible
3
a
or rigid
3
b
ring systems by Fodor and Kiss. More recently, McCasland
4
elucidated the configuration of the epimeric inosamines by the same means. |
| doi_str_mv | 10.1038/169462a0 |
| format | Article |
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1
, chloromycetin
2
, as well as for that of the alicyclic amino-alcohols (2-amino-
cyclo
hexanol and pentanols) containing flexible
3
a
or rigid
3
b
ring systems by Fodor and Kiss. More recently, McCasland
4
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1
, chloromycetin
2
, as well as for that of the alicyclic amino-alcohols (2-amino-
cyclo
hexanol and pentanols) containing flexible
3
a
or rigid
3
b
ring systems by Fodor and Kiss. More recently, McCasland
4
elucidated the configuration of the epimeric inosamines by the same means.</description><subject>Humanities and Social Sciences</subject><subject>letter</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1952</creationdate><recordtype>article</recordtype><recordid>eNptz01LxDAQBuAgCtZV8BdIj3qITj6apEdZXBUWPLieS5pMtYvblKQ97L-30l28OJeB4eFlXkKuGdwzEOaBqVIqbuGEZExqRaUy-pRkANxQMEKdk4uUtgBQMC0zQt8HjBjcF-7aNMR9Hpp8E0Pfdpjbzud9wtEHejhdkrPGfie8OuwF-Vg9bZYvdP32_Lp8XFPHDR-o1MYoXZtClSgYk8px4dBKXcsGODBvjGfTCAPecVRQlKXCWhTMWo9YiAW5nXNdDClFbKo-tjsb9xWD6rdmdaw50buZpol0nxirbRhjN333n72ZbWeHMeJf6BH8AA-wWpI</recordid><startdate>19520315</startdate><enddate>19520315</enddate><creator>FODOR, G</creator><creator>NÁDOR, K</creator><general>Nature Publishing Group UK</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19520315</creationdate><title>Stereochemistry of Tropine and pseudo-Tropine</title><author>FODOR, G ; NÁDOR, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-478867b8569e31146c23cea47b4f0201d88d1111380dc2e605996eb351aadee53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1952</creationdate><topic>Humanities and Social Sciences</topic><topic>letter</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FODOR, G</creatorcontrib><creatorcontrib>NÁDOR, K</creatorcontrib><collection>CrossRef</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FODOR, G</au><au>NÁDOR, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stereochemistry of Tropine and pseudo-Tropine</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><date>1952-03-15</date><risdate>1952</risdate><volume>169</volume><issue>4298</issue><spage>462</spage><epage>463</epage><pages>462-463</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>ACYL migration N → O was used for the determination of the configuration of the diastereomeric 1.2-amino-alcohols, for example, ephedrine
1
, chloromycetin
2
, as well as for that of the alicyclic amino-alcohols (2-amino-
cyclo
hexanol and pentanols) containing flexible
3
a
or rigid
3
b
ring systems by Fodor and Kiss. More recently, McCasland
4
elucidated the configuration of the epimeric inosamines by the same means.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/169462a0</doi><tpages>2</tpages></addata></record> |
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| language | eng |
| recordid | cdi_crossref_primary_10_1038_169462a0 |
| source | Nature; SpringerLink Journals - AutoHoldings |
| subjects | Humanities and Social Sciences letter multidisciplinary Science Science (multidisciplinary) |
| title | Stereochemistry of Tropine and pseudo-Tropine |
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