Stereoelectronic effects on π-facial selectivity in addition to 4H- 1,3-dioxin-4-ones

Chemical and Pharmaceutical Bulletin

Volumn 47, Issue 2, 1999, Pages 293-294

  Uehara, Fumiaki ^a   Sato, Masayuki ^a,b   Kaneko, Chikara ^a  

^a TOHOKU UNIVERSITY   (Japan)

^b UNIVERSITY OF SHIZUOKA   (Japan)

Author keywords

4H 1,3 dioxin 4 one; Asymmetric addition; Conformation analysis; Stereoelectronic effect

Indexed keywords

4H 1,3 DIOXIN 4 ONE; DIOXIN; UNCLASSIFIED DRUG;

ARTICLE; DERIVATIZATION; DRUG CONFORMATION; DRUG EFFECT; DRUG SYNTHESIS; HYDROGENATION; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY;

EID: 0032962682     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.47.293     Document Type: Article

References (22)

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18. Hydrogenolysis of 2e with Pd-C catalyst gave the carboxylic acid, treatment of which with p-TsCl and then with amine hydrochlorides in pyridine furnished 2c and 2d, respectively.
19. MOPAC PM3 calculations were done on a Tektronix CAChe work system.
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