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Chirality control by the aid of 2:2-dimethyloxazolidine chiral auxiliaries. Highly 1:4-chiral inductive asymmetric alkylations of amide enolates

✍ Scribed by Shuji Kanemasa; Koichi Ueno; Kenjiro Onimura; Takashi Kikukawa; Hidetoshi Yamamoto

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Chirality Control b

✍ S. KANEMASA; K. UENO; K. ONIMURA; T. KIKUKAWA; H. YAMAMOTO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB

Chiral 4-Phenyl-2-trifluoromethyloxazoli

✍ Arnaud Tessier; Julien Pytkowicz; Thierry Brigaud 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 43 KB

Chiral 4-Phenyl-2-trifluoromethyloxazoli

✍ Arnaud Tessier; Julien Pytkowicz; Thierry Brigaud 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 126 KB

Chiral 4-Phenyl-2-trifluoromethyloxazoli

✍ Arnaud Tessier; Julien Pytkowicz; Thierry Brigaud 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 126 KB

ChemInform Abstract: Effective Enantioco

✍ S. KANEMASA; H. SUENAGA; K. ONIMURA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

Bifunctional chiral auxiliaries 4: Alkyl

✍ Stephen G. Davies; Andrew A. Mortlock 📂 Article 📅 1992 🏛 Elsevier Science 🌐 French ⚖ 273 KB

Addition of alkyl halides to sodium and potassium enolates of 1,3-diacyl-trans-4,5-