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Volumn 57, Issue 31, 2001, Pages 6815-6822
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A joint experimental and ab initio study on the reactivity of several hydroxy selenides. Stereoselective synthesis of cis-disubstituted tetrahydrofurans via seleniranium ions
a
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Author keywords
Cyclizations; Oxygen heterocycles; Selenium; Theoretical studies
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Indexed keywords
1 (BENZYLOXY) 4 PHENYLSELENYLHEPTAN 2,5,7 TRIOL;
1 (BENZYLOXY) 5 PHENYLSELENYLHEPTAN 2,4,7 TRIOL;
1 (BENZYLOXY) 7 (TRIISOPROPYLSILYLOXY) 4 PHENYLSELENYLHEPTAN 2,5 DIOL;
1 (BENZYLOXY) 7 (TRIISOPROPYLSILYLOXY) 5 PHENYLSELENYLHEPTAN 2,4 DIOL;
1,6 (DIBENZYLOXY) 2 PHENYLSELENYLHEXAN 3,5 DIOL;
1,6 (DIBENZYLOXY) 3 PHENYLSELENYLHEXAN 2,5 DIOL;
1,7 (DIBENZYLOXY) 4 PHENYLSELENYLHEPTAN 2,5 DIOL;
1,7 (DIBENZYLOXY) 5 PHENYLSELENYLHEPTAN 2,4 DIOL;
2 BENZYLOXYETHYL 3 PHENYLSELENYL 5 BENZYLOXYMETHYL TETRAHYDROFURAN;
2 HYDROXYETHYL 3 PHENYLSELENYL 5 BENZYLOXYMETHYL TETRAHYDROFURAN;
2,5 DIBENZYLOXYMETHYL 3 PHENYLSELENYL TETRAHYDROFURAN;
HYDROXYL GROUP;
HYDROXYSELENIDE DERIVATIVE;
PERCHLORIC ACID;
SELENIRANIUM ION;
SELENIUM;
SELENIUM DERIVATIVE;
TETRAHYDROFURAN DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
ATOM;
CATALYSIS;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
PRIORITY JOURNAL;
REACTION ANALYSIS;
STEREOCHEMISTRY;
STOICHIOMETRY;
SYNTHESIS;
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EID: 0035974349
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)00618-4 Document Type: Article |
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Times cited : (22)
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References (34)
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