✦ LIBER ✦

Enzymatic synthesis of propargylamides

✍ Scribed by Francisca Rebolledo; Rosario Brieva; Vicente Gotor

Book ID: 104244865
Publisher: Elsevier Science
Year: 1989
Tongue: French
Weight: 127 KB
Volume: 30
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)93782-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

PIDA-mediated synthesis of oxazoles thro

PIDA-mediated synthesis of oxazoles through oxidative cycloisomerization of propargylamides

✍ Akio Saito; Asami Matsumoto; Yuji Hanzawa 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 428 KB

PIDA [phenyliodine(III) diacetate] in AcOH or AcOH-HFIP (hexafluoroisopropanol) efficiently promotes the formation of 2,5-disubstituted oxazoles via the oxidative cycloisomerization of propargylamide derivatives.

Asymmetric Synthesis of Propargylamides

Asymmetric Synthesis of Propargylamides via 3,3′-Disubstituted Binaphthol-Modified Alkynylboronates.

✍ T. Robert Wu; J. Michael Chong 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 52 KB 👁 1 views

Asymmetric Synthesis of Propargylamides

Asymmetric Synthesis of Propargylamides via 3,3‘-Disubstituted Binaphthol-Modified Alkynylboronates

✍ Wu, T. Robert; Chong, J. Michael 📂 Article 📅 2006 🏛 American Chemical Society 🌐 English ⚖ 77 KB

Intramolecular Pd(II)-Catalyzed Cyclizat

Intramolecular Pd(II)-Catalyzed Cyclization of Propargylamides: Straightforward Synthesis of 5-Oxazolecarbaldehydes

✍ Beccalli, Egle M.; Borsini, Elena; Broggini, Gianluigi; Palmisano, Giovanni; Sot 📂 Article 📅 2008 🏛 American Chemical Society 🌐 English ⚖ 144 KB

Amphiphilic Poly(N-propargylamide) with

Amphiphilic Poly(N-propargylamide) with Galactose and Lauryloyl Groups: Synthesis and Properties

✍ Masakazu Suenaga; Yoshiro Kaneko; Jun-ichi Kadokawa; Takehiro Nishikawa; Hidezo 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 343 KB

## Abstract **Summary:** An amphiphilic poly(__N__‐propargylamide) with galactose and lauryloyl groups was synthesized by copolymerization of the corresponding __N__‐propargylamide monomers using a Rh catalyst. The obtained copolymer formed a one‐handed helical conformation and molecular aggregates

Synthesis of oxazoles through Pd-catalyz

Synthesis of oxazoles through Pd-catalyzed cycloisomerization–allylation of N-propargylamides with allyl carbonates

✍ Akio Saito; Koichi Iimura; Yuji Hanzawa 📂 Article 📅 2010 🏛 Elsevier Science 🌐 French ⚖ 816 KB

In the presence of Pd 2 (dba) 3 -Cy 3 P catalyst, IPrÁHCl salt [IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2ylidene], and Cs 2 CO 3 , N-propargylamides react with allyl carbonates to give 2,5-disubstituted oxazoles having homoallyl groups through the tandem cycloisomerization-allylation.