A convenient one-pot completely stereoselective synthesis of trans-4-Hydroxystilbenes and its derivatives and X-ray structure of its precursor

Synthetic Communications

Volumn 33, Issue 14, 2003, Pages 2519-2530

  Chhor, Rakeshwar B ^a   Singh, Kunwar A ^b   Nosse, B ^a   Tandon, Vishnu K ^b  

^a UNIVERSITY OF REGENSBURG   (Germany)

^b UNIVERSITY OF LUCKNOW   (India)

Author keywords

Fries rearrangement; Reductive elimination; Stereoselective; trans 4 Hydroxystilbene; X ray structure

Indexed keywords

2 CHLORO 4 HYDROXYSTILBENE; 2 METHYL 4 HYDROXYSTILBENE; 2 PHENYL 1 (4 HYDROXY 1 NAPHTHYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 2 CHLOROPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 2 METHYLPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 2,5 DIMETHYLPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 2,6 DIMETHYLPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 3 CHLOROPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 3 METHOXYPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 3 METHYLPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (4 HYDROXY 3 NITROPHENYL)ETHAN 1 ONE; 2 PHENYL 1 (6 HYDROXY 1 NAPHTHYL)ETHAN 1 ONE; 2 PHENYL(4 HYDROXYPHENYL)ETHAN 1 ONE; 2,5 DIMETHYL 4 HYDROXYSTILBENE; 2,6 DIMETHYL 4 HYDROXYSTILBENE; 3 CHLORO 4 HYDROXYSTILBENE; 3 METHOXY 4 HYDROXYSTILBENE; 3 METHYL 4 HYDROXYSTILBENE; 3 NITRO 4 HYDROXYSTILBENE; 4 (2 PHENYLVINYL) 1 NAPHTHOL; 4 HYDROXYSTILBENE; 5 (2 PHENYLVINYL) 1 NAPHTHOL; KETONE DERIVATIVE; STILBENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CRYSTAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; ISOMER; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY;

EID: 0042564664     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120021843     Document Type: Article

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