The Baylis-Hillman reaction: An expedient synthesis of (Z)-keto allyl bromides and chlorides

Tetrahedron

Volumn 55, Issue 22, 1999, Pages 6971-6976

  Basavaiah, Deevi ^a   Hyma, Rachakonda Suguna ^a   Padmaja, Kisari ^a   Krishnamacharyulu, Marimganti ^a  

^a UNIVERSITY OF HYDERABAD   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BROMINE DERIVATIVE; CHLORIDE;

ARTICLE; CHEMICAL BOND; CHEMICAL PROCEDURES; CHEMICAL REACTION; CHEMICAL STRUCTURE; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0033612106     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00326-9     Document Type: Article

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21. 1H NMR spectrum of 2a the vinylic proton appears at δ 7.64 (partly merged with aromatic protons). Therefore we assigned (Z)-stereochemistry to 2a.
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