✦ LIBER ✦

Stereospecific anionic polymerization of chiral benzyl α-[(1-phenylethoxy)methyl]acrylate

✍ Scribed by Takahiro Uno; Shigeki Habaue; Yoshio Okamoto

Publisher: John Wiley and Sons
Year: 1998
Tongue: English
Weight: 139 KB
Volume: 10
Category: Article
ISSN: 0899-0042
DOI: 10.1002/(sici)1520-636x(1998)10:7<711::aid-chir18>3.0.co;2-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Stereospecific polymerization of benzyl

Stereospecific polymerization of benzyl α-(alkoxymethyl) acrylates

✍ Shigeki Habaue; Hiroshi Yamada; Takahiro Uno; Yoshio Okamoto 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 158 KB

a-(Alkoxymethyl)acrylates, such as methyl a-(phenoxymethyl)acrylate, benzyl a-(methoxymethyl)acrylate (BMMA), benzyl a-(benzyloxymethyl)acrylate, and benzyl a-(tert-butoxymethyl)acrylate, were synthesized, and their polymerizability and the stereoregularity of the polymers obtained by radical and an

Photoinduced Electron Transfer (PET) Pro

Photoinduced Electron Transfer (PET) Promoted Oxidative Activation of 1-(N-Benzyl-N-methylglycyl)-(S)-prolinol: Development of Novel Strategies Towards Enantioselective Syntheses of α-Amino Acids, Their N-Methyl Derivatives and α-Hydroxy Acids Employing (S)-Prolinol as aRecyclable Chiral Auxiliary

✍ Ganesh Pandey; Parthasarathi Das; P. Yella Reddy 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB 👁 1 views

Photoinduced electron transfer (PET) / Enantioselective syntheses / α-Amino acids / α-Hydroxy acids / (S)-Prolinol / Recyclable chiral auxiliary PET activation of 1-(N-benzyl-N-methylglycyl)-(S)-prolinol (1) in dry acetonitrile, utilizing 1,4-dicyanonaphthalene (DCN) as a light-harvesting electron-a