Enantioselective esterification of 5-hydroxy-2-methyl-6-(diethoxy-methyl)-1-cyclohexenecarbaldehyde. Synthesis of both enantiomers of 6-methylbicyclo[4.1.0]hept-2-ene-1,2-dicarbaldehyde

Tetrahedron: Asymmetry

Volumn 6, Issue 2, 1995, Pages 595-602

  Gustafsson, Jörgen ^a   Sandström, Jan ^a   Sterner, Olov ^a  

^a LUND UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

6 METHYLBICYCLO[4.1.0]HEPT 2 ENE 1,2 DICARBALDEHYDE; BICYCLO COMPOUND; BICYCLO[4.1.0]HEPTANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CIRCULAR DICHROISM; DRUG SYNTHESIS; ENANTIOMER; ESTERIFICATION; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0028954631     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00043-O     Document Type: Article

References (24)

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3. Enzymatic preparation of enantiomerically pure and selectively protected 1,2- and 1,3-diols
4. Exciton chirality methods as applied to conjugated enones, esters, and lactones
5. The Exciton Chirality Method
6. Rotatory properties of molecules containing two peptide groups: theory
7. 329. Studies in the polyene series. Part III