✦ LIBER ✦

Total synthesis of (.+-.)-maytansinol. The common precursor to the maytansinoids

✍ Scribed by Meyers, A. I.; Reider, Paul J.; Campbell, Arthur L.

Book ID: 121312475
Publisher: American Chemical Society
Year: 1980
Tongue: English
Weight: 259 KB
Volume: 102
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00541a054

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Progress toward the total synthesis of m

Progress toward the total synthesis of maytansinoids. An efficient route to two major precursors (western-southern zone)

✍ A.I. Meyers; Kiyoshi Tomioka; Dennis M. Roland; Daniel Comins 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 264 KB

Studies related to the synthesis of mayt

✍ Derek H.R. Barton; Michel Bénéchie; Françoise Khuong-Huu; Pierre Potier; Victor 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 196 KB

Two approaches to the partial synthesis of C1-Cs of a bis-nor maytansinoid 1 have been investigated starting on the one hand with (S)-(-)-malic acid and on the other, with D-(+)-ribonolactone. 2 Maytansinoids are interesting naturally occurringIantitumor agents . 3 Extensive work has already been ca

Progress toward the total synthesis of m

Progress toward the total synthesis of maytansinoids. Synthesis of (.+-.)-4,5-deoxymaysine (N-methylmaysenine)

✍ Meyers, A. I.; Roland, Dennis M.; Comins, Daniel L.; Henning, Rainer; Fleming, M 📂 Article 📅 1979 🏛 American Chemical Society 🌐 English ⚖ 390 KB

Progress toward the total synthesis of m

Progress toward the total synthesis of maytansinoids. A facile route to the aromatic moiety (western zone)

✍ John M. Kane; A.I. Meyers 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 164 KB

On the total synthesis of (S)-methanophe

On the total synthesis of (S)-methanophenazine and the formal synthesis of (R)-methanophenazine from a common precursor

✍ Uwe Beifuss; Mario Tietze 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 79 KB

Methanophenazine is a new cofactor from methanogenic archaea. (S)-Methanophenazine has been synthesized from three building blocks, i.e. 2-hydroxy-phenazine, ethyl (R)-3-methylglutarate and (E,E)farnesyl acetone; a stereodivergent approach from ethyl (R)-3-methylglutarate warrants the formal synthes

The asymmetric total synthesis of (−)-de

The asymmetric total synthesis of (−)-dehydrovomifoliol. The penultimate precursor to (−)-abscisic acid (ABA)

✍ A.I. Meyers; Michael A. Sturgess 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 220 KB