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Volumn 1, Issue 11, 1999, Pages 1775-1777

Solvent-dependent stereoselectivity of bis-2-pyridone [4 + 4] photocycloaddition is due to H-bonded dimers

Author keywords

[No Author keywords available]

Indexed keywords

PYRIDONE DERIVATIVE; SOLVENT;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; CYCLIZATION; DIMERIZATION; HYDROGEN BOND; LIGHT; RADIATION EXPOSURE; STEREOISOMERISM;

CYCLIZATION; DIMERIZATION; HYDROGEN BONDING; LIGHT; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PYRIDONES; SOLVENTS; STEREOISOMERISM;

EID: 0033518060 PISSN: 15237060 EISSN: None Source Type: Journal
DOI: 10.1021/ol991058p Document Type: Article

Times cited : (24)

References (13)

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- Sieburth, S.McN.¹

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5
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6
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- and the steric effects of pyridone solvation (ref 4). Hydrogen bonding of 4a to solvent would enhance both of these effects
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