Source:http://linkedlifedata.com/resource/pubmed/id/21615116
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2011-6-10
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pubmed:abstractText |
A straightforward, highly stereoselective protocol toward the synthesis of deuterium-labeled (2R,3S,4S)-?-cyclohexenylserine has been developed. Key steps are a Nozaki-Hiyama-Kishi reaction generating the stereogenic centers and a ring-closing metathesis for the construction of the cyclohexenyl ring system. The labeled amino acid was further activated as an SNAc-ester for feeding experiments.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cyclohexenes,
http://linkedlifedata.com/resource/pubmed/chemical/Deuterium,
http://linkedlifedata.com/resource/pubmed/chemical/Lactones,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles,
http://linkedlifedata.com/resource/pubmed/chemical/Serine,
http://linkedlifedata.com/resource/pubmed/chemical/marizomib
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1523-7052
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pubmed:author | |
pubmed:copyrightInfo |
© 2011 American Chemical Society
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pubmed:issnType |
Electronic
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pubmed:day |
17
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3210-3
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pubmed:meshHeading | |
pubmed:year |
2011
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pubmed:articleTitle |
Stereoselective synthesis of deuterated ?-cyclohexenylserine, a biosynthetic intermediate of the salinosporamides.
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pubmed:affiliation |
Universita?t des Saarlandes, Institut fu?r Organische Chemie, Im Stadtwald, Geb. C4.2, D-66123 Saarbru?cken, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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