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Volumn 58, Issue 16, 2002, Pages 3249-3262
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The Diels-Alder reactivity of nitrobenzofuroxans: Mono- and di-adducts of isoprene and 2,3-dimethylbutadiene. New convenient precursors to naphtho- and phenanthreno-furoxanic and -furazanic structures
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Author keywords
Diels Alder adducts; Nitrobenzofuroxans; Phenanthrenofuroxanic structures; Precursor; Rearomatization; Stereoselectivity
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Indexed keywords
1,3 BUTADIENE DERIVATIVE;
2,3 DIMETHYLBUTADIENE;
4 NITRO 6 TRIFLUOROMETHANESULFONYLBENZOFUROXAN;
4 TRIFLUOROMETHYL 6 NITROBENZOFUROXAN;
4,6 DINITROBENZOFUROXAN;
4,6 DINITROTETRAZOLO[1,5 A]PYRIDINE;
6 CYANO 4 NITROBENZOFUROXAN;
6 TRIFLUOROMETHYL 4 NITROBENZOFUROXAN;
AZAPHENANTHRENOTETRAZOLE;
ISOPRENE;
NITROBENZENE DERIVATIVE;
NITROUS ACID;
PYRIDINE DERIVATIVE;
TETRAZOLE DERIVATIVE;
UNCLASSIFIED DRUG;
AROMATIZATION;
ARTICLE;
CHEMICAL BOND;
CHEMICAL REACTION;
CRYSTAL STRUCTURE;
DIELS ALDER REACTION;
MOLECULE;
OXIDATION;
POLYMERIZATION;
PRIORITY JOURNAL;
STEREOCHEMISTRY;
STEREOSPECIFICITY;
X RAY CRYSTALLOGRAPHY;
BETULACEAE;
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EID: 0037090552
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(02)00236-3 Document Type: Article |
Times cited : (37)
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References (76)
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