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A new synthesis of serricornin [(4s,6s,7s)-7-hydroxy-4,6-dimethyl-3-nonanone], the sex pheromone of the cigarette beetle

✍ Scribed by Kenji Mori; Hidenori Watanabe

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and absolute stereochemistry o

✍ Kenji Mori; Hiroko Nomi; Tatsuji Chuman; Masahiro Kohno; Kunio Kato; Masao Noguc 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 751 KB

Inhibitory action of (4S,6S,7R)-isomer t

✍ M. Mori; K. Mochizuki; M. Kohno; T. Chuman; A. Ohnishi; H. Watanabe; K. Mori 📂 Article 📅 1986 🏛 Springer 🌐 English ⚖ 457 KB

Determination of the absolute configurat

✍ Kenji Mori; Hiroko Nomi (née Iwasawa); Tatsuji Chuman; Masahiro Kohno; Kunio Kat 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 228 KB

The absolute configuration at C-6 and C-7 of serricornin was established as (6S, 75) by synthesizing its (65, 7S)-erythro and (6R, 7R)threo isomers.

A stereoselective synthesis of “natural”

✍ Masataka Mori; Tatsuji Chuman; Kunio Katō; Kenji Mori 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 231 KB

Synthesis of (4 R ,6 S ,7 R )-7-Hydroxy-

✍ MASUDA, Yui; FUJITA, Ken; MORI, Kenji 📂 Article 📅 2003 🏛 Japan Science and Technology Information Aggregato 🌐 English ⚖ 300 KB

Synthesis of (4R,6S,7R)-7-hydroxy-4,6-di

✍ Gowravaram Sabitha; Chitti Srinivas; Chittapragada Maruthi; Jhillu Singh Yadav 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 536 KB