Stereospecific Construction of Contiguous Quaternary and Tertiary Stereocenters by Rearrangement from Indoline-2-methanol to 2,2,3-Trisubstituted Tetrahydroquinoline: Application to an Efficient Total Synthesis of Natural Virantmycin.

Stereospecific Construction of Contiguou

Stereospecific Construction of Contiguous Quaternary and Tertiary Stereocenters by Rearrangement from Indoline-2-methanol to 2,2,3-Trisubstituted Tetrahydroquinoline: Application to an Efficient Total Synthesis of Natural Virantmycin

✍ Mayuko Ori; Narihiro Toda; Kazuko Takami; Keiko Tago; Hiroshi Kogen 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 124 KB

Stereospecific Construction of Contiguou

Stereospecific Construction of Contiguous Quaternary and Tertiary Stereocenters by Rearrangement from Indoline-2-methanol to 2,2,3-Trisubstituted Tetrahydroquinoline: Application to an Efficient Total Synthesis of Natural Virantmycin

✍ Mayuko Ori; Narihiro Toda; Kazuko Takami; Keiko Tago; Hiroshi Kogen 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 124 KB

The stereoselective construction of chiral quaternary stereocenters is one of the most challenging problems in synthetic organic chemistry. [1] Substituted tetrahydroquinolines and tetrahydroisoquinolines have attracted considerable attention from organic and medicinal chemists, primarily because th

Stereospecific Synthesis of 2,2,3-Trisub

Stereospecific Synthesis of 2,2,3-Trisubstituted Tetrahydroquinolines: Application to the Total Syntheses of Benzastatin E and Natural Virantmycin.

✍ Mayuko Ori; Narihiro Toda; Kazuko Takami; Keiko Tago; Hiroshi Kogen 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

Stereospecific Synthesis of 2,2,3-Trisub

Stereospecific Synthesis of 2,2,3-Trisubstituted Tetrahydroquinolines: Application to the Total Syntheses of Benzastatin E and Natural Virantmycin.

✍ Mayuko Ori; Narihiro Toda; Kazuko Takami; Keiko Tago; Hiroshi Kogen 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 35 KB