Synchronized stereocontrol of planar chirality by crystallization-induced asymmetric transformation

Tetrahedron Letters

Volumn 50, Issue 4, 2009, Pages 409-412

  Kanomata, Nobuhiro ^a   Mishima, Gou ^b   Onozato, Jun ^b  

^a WASEDA UNIVERSITY   (Japan)

^b MEIJI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BUTANOL; CYCLOPHANE DERIVATIVE; NICOTINIC ACID DERIVATIVE;

ARTICLE; ASYMMETRIC CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CRYSTALLIZATION; DIASTEREOISOMER; PHASE TRANSITION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 57149140845     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.11.021     Document Type: Article

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39. ext = 283 (Δε -18.4), 261 (-1.3), 230 (-40.1), 203.7 (+20.5).
40. p)-5b (column: Chiralcel OD, Dicel Chemical Industries, Ltd; Mobile phase: 5% IPA in hexane; flow rate: 2.0 mL/min; oven temperature: 25 °C).
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43. ext = 283 (Δε -6.9), 262 (-1.7), 232 (-20.3), 205 (+18.7).
44. ext = 282 (Δε -14.8), 259 (+3.9), 233 (-60.5).
45. p)-7. The ratio was determined by HPLC analysis using CHIRALPAK IA, Dicel Chemical Industries, Ltd, with hexane/ethyl acetate (2/1) as a mobile phase (flow rate: 1.0 mL/min; oven temperature: 40 °C).