Edema and fibrosis imaging by cardiovascular magnetic resonance: How can the experience of Cardiology be best utilized in rheumatological practice?

Stereoselective Construction of 3a-Methylhydrindans Starting from 2,7-Enynol Derivatives Based on Ti(II)-Mediated Cyclization and Ru-Catalyzed Ring-Closing Metathesis. -The efficient two-step method developed for the diastereoselective construction of tetrahydroindenes can also be applied to other ring systems. -(OHKUBO, M.; UCHIKAWA, W.; MATSUSHITA, H.; NAKANO, A.; SHIRATO, T.; OKAMOTO*, S.; Tetrahedron Lett. 47 (2006) 29, 5181-5185; Dep. Appl. Chem., Fac. Eng., Kanagawa Univ., Kanagawa, Yokohama 221, Japan; Eng.) -Mais 44-106

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Wataru Uchikawa

Use of CaH2 as a reductive hydride source: reduction of ketones and imines with CaH2/ZnX2 in the presence of a Lewis acid

Formation of azatitanacyclopentanes from ene-imines and a Ti(O-i-Pr)4/2i-PrMgX reagent and their synthetic reactions

Stereoselective construction of 3a-methylhydrindanes starting from 2,7-enynol derivatives based on Ti(II)-mediated cyclization and Ru-catalyzed ring-closing metathesis

Formation of Azatitanacyclopentanes from Ene-Imines and a Ti(O-iPr)4/2iPrMgX Reagent and Their Synthetic Reactions.

Use of CaH₂ as a Reductive Hydride Source: Reduction of Ketones and Imines with CaH₂/ZnX₂ in the Presence of a Lewis Acid.

Stereoselective Construction of 3a‐Methylhydrindans Starting from 2,7‐Enynol Derivatives Based on Ti(II)‐Mediated Cyclization and Ru‐Catalyzed Ring‐Closing Metathesis.

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Wataru Uchikawa

Use of CaH2 as a reductive hydride source: reduction of ketones and imines with CaH2/ZnX2 in the presence of a Lewis acid

Formation of azatitanacyclopentanes from ene-imines and a Ti(O-i-Pr)4/2i-PrMgX reagent and their synthetic reactions

Stereoselective construction of 3a-methylhydrindanes starting from 2,7-enynol derivatives based on Ti(II)-mediated cyclization and Ru-catalyzed ring-closing metathesis

Formation of Azatitanacyclopentanes from Ene-Imines and a Ti(O-iPr)4/2iPrMgX Reagent and Their Synthetic Reactions.

Use of CaH2 as a Reductive Hydride Source: Reduction of Ketones and Imines with CaH2/ZnX2 in the Presence of a Lewis Acid.

Stereoselective Construction of 3a‐Methylhydrindans Starting from 2,7‐Enynol Derivatives Based on Ti(II)‐Mediated Cyclization and Ru‐Catalyzed Ring‐Closing Metathesis.

Contact Info

Product

Resources

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Use of CaH₂ as a Reductive Hydride Source: Reduction of Ketones and Imines with CaH₂/ZnX₂ in the Presence of a Lewis Acid.