The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety
- 3 June 1996
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 35 (10) , 1093-1096
- https://doi.org/10.1002/anie.199610931
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- The First Syntheses of 6‐/10‐Membered Ring Analogs and of a 6‐/11‐Membered Ring Analog of the Dienediyne Core of the Neocarzinostatin Chromophore by Ring‐Closure According to the Nozaki‐Hiyama ReactionEuropean Journal of Organic Chemistry, 1996
- Synthesis of 6‐/10‐Membered Ring Analogs of the Dienediyne Core of the Neocarzinostatin Chromophore by Palladium(0)‐Mediated Ring‐Closure ReactionsEuropean Journal of Organic Chemistry, 1996
- Synthese neuer Dehydroannulene vom Sworski‐Typ:3,4‐Benz‐1,2,5,6,8,9,12, 13‐octadehydro[14]annuleneAngewandte Chemie, 1995
- Totalsynthese von (±)‐Dynemicin AAngewandte Chemie, 1995
- The First 6-Membered/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatin ChromophoreTetrahedron Letters, 1995
- Low Valent Titanium - A versatile reagent for deoxygenation and carbonyl coupling. 11Advanced Synthesis & Catalysis, 1995
- Der Kampf um Calicheamicin γ**Angewandte Chemie, 1993
- Titanium‐Catalyzed Epoxy–Hydroxylation of Allylic Alcohols: A Convenient Diastereoselective Synthesis of Epoxy DiolsAngewandte Chemie International Edition in English, 1993
- Vanadium-catalyzed epoxidations. 2. Highly stereoselective epoxidations of acyclic homoallylic alcohols predicted by a detailed transition-state modelJournal of the American Chemical Society, 1981
- Über die Ester der halogenierten Alkohole. (II. Mitteilung). „Über die Reaktionen der Ester, die die Trichlormethoxylgruppe enthalten”︁Journal für Praktische Chemie, 1930