Molecular library synthesis using complex substrates: Expanding the framework of triterpenoids

Journal of Organic Chemistry

Volumn 78, Issue 2, 2013, Pages 410-418

  Ignatenko, Vasily A ^a   Han, Yong ^a   Tochtrop, Gregory P ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL LIBRARIES; CHEMICAL SPACE; COMPLEX SUBSTRATES; CONFORMATIONAL ANALYSIS; DIVERSITY-ORIENTED SYNTHESIS; INHERENT COMPLEXITY; MOLECULAR LIBRARIES; NATURAL PRODUCTS; PROOF OF PRINCIPLES; TRITERPENOIDS;

CHEMICAL COMPOUNDS;

SYNTHESIS (CHEMICAL);

METHYL 10 ACETOXY 12B HYDROXY 2,4A,6A,9,9,12A,14A HEPTAMETHYL 7 OXODOCOSAHYDROBENZO[A]NAPHTHO[2,1 F]AZULENE 2 CARBOXYLATE; METHYL 10 ACETOXY 2,4A,6A,6B,9,9,12A HEPTAMETHYL 13 OXO 1,2,3,4,4A,5,6,6A,6B,7,8,8A,9,10,11,12,12A,13,13A,14 ICOSAHYDROBENZO[F]NAPHTHA[2,1 ALPHA]AZULENE 2 CARBOXYLATE; METHYL 10 ACETOXY 2,4A,6A,9,9,12A,14A HEPTAMETHYL 7 OXO 1,2,3,4,4A,5,6,6A,7,8,8A,9,10,11,12,12A,13,14,14A,14B ICOSAHYDROBENZO[A]NAPHTHO[2,1 F]AZULENE 2 CARBOXYLATE; METHYL 10 ACETOXY 2,4A,6A,9,9,12B,14A HEPTAMETHYL 7 OXO 1,2,3,4,4A,5,6,6A,7,7A,8,9,10,11,12,12B,13,14,14A,14B ICOSAHYDROBENZO[A]NAPHTHO[2,1 F]AZULENE 2 CARBOXYLATE; METHYL 10 ACETOXY 6B HYDROXY 2,4A,6A,9,9,12A,14A HEPTAMETHYL 13 OXODOCOSAHYDROBENZO[F ]NAPHTHO[2,1 ALPHA]AZULENE 2 CARBOXYLATE; METHYL 11 ACETOXY 2,4A,6A,10,10,13A,16A HEPTAMETHYL 7,8,14 TRIOXODOCOSAHYDROBENZO[6,7]CYCLODECA[1,2 ALPHA]NAPHTHALENE 2 CARBOXYLATE; METHYL 11 ACETOXY 2,4A,6A,10,10,13A,16A HEPTAMETHYL 7,8,14,15 TETRAOXODOCOSAHYDROBENZO[6,7]CYCLODECA[1,2 ALPHA]NAPHTHALENE 2 CARBOXYLATE; METHYL 11 ACETOXY2,4A,6A,10,10,13A,16A HEPTAMETHYL 7,14 DIOXODOCOSAHYDROBENZO[6,7]CYCLODECA[1,2 ALPHA]NAPHTHALENE 2 CARBOXYLATE; TRITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; COMPLEX FORMATION; MOLECULAR LIBRARY; STEREOCHEMISTRY; SYNTHESIS;

CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; MOLECULAR CONFORMATION; SMALL MOLECULE LIBRARIES; TRITERPENES;

EID: 84872516295     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo302211f     Document Type: Article

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