The chalcogeno-Baylis-Hillman reaction: A new preparation of allylic alcohols from aldehydes and electron-deficient alkenes

Tetrahedron

Volumn 54, Issue 39, 1998, Pages 11813-11824

  Kataoka, Tadashi ^a   Iwama, Tetsuo ^a   Tsujiyama, Shin Ichiro ^a   Iwamura, Tatsunori ^a   Watanabe, Shin Ichi ^a  

^a GIFU PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL ALCOHOL;

ARTICLE; CATALYSIS; CHEMICAL REACTION; ENANTIOMER; PRIORITY JOURNAL; REACTION ANALYSIS; REACTION TIME; SYNTHESIS;

EID: 0032564002     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)83041-X     Document Type: Article

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29. The product 24 and p-nitrobenzaldehyde were overlapped each other on pareparative TLC, therefore, we did not isolate 24 in the chalcogeno-Baylis-Hillman reaction described in Tables 1 and 2. We did not also isolate chlorides in the reactions shown in Table 3.
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