Synthetic studies towards optically active 13-oxyingenol via asymmetric cyclopropanation

Synthesis

Volumn , Issue 5, 2011, Pages 769-777

  Hayakawa, Ichiro ^a   Miyazawa, Yamato ^a   Ohyoshi, Takayuki ^a   Asuma, Yuki ^a   Aoki, Kenta ^a   Kigoshi, Hideo ^a  

^a UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

13 oxyingenol; asymmetric cyclopropanation; chiral aza semicorrin ligand; intramolecular aldol reaction; reductive deoxygenation

Indexed keywords

13-OXYINGENOL; ASYMMETRIC CYCLOPROPANATION; CHIRAL AZA-SEMICORRIN LIGAND; DEOXYGENATIONS; INTRAMOLECULAR -ALDOL REACTION;

CONDENSATION REACTIONS; LIGANDS;

SYNTHESIS (CHEMICAL);

13 OXYINGENOL; DITERPENOID; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CYCLIZATION; CYCLOPROPANATION; DEOXYGENATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; RACEMIC MIXTURE; RING CLOSING METATHESIS; STEREOCHEMISTRY;

EID: 79951855626     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1259430     Document Type: Article

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