✦ LIBER ✦

An efficient solid-phase synthesis of 3-substituted and 3,3-disubstituted 1,2-dialkylpyrazolidine-3,5-diones

✍ Scribed by He, Rongjun; Lam, Yulin

Book ID: 118736497
Publisher: Royal Society of Chemistry
Year: 2008
Tongue: English
Weight: 193 KB
Volume: 6
Category: Article
ISSN: 1477-0520
DOI: 10.1039/B802648C

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Efficient solid phase synthesis of 3,5-d

Efficient solid phase synthesis of 3,5-disubstituted hydantoins

✍ Adel Nefzi; John M. Ostresh; Marc Giulianotti; Richard A. Houghten 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 170 KB

Solid-phase synthesis of 1,2,4-triazolid

Solid-phase synthesis of 1,2,4-triazolidine-3,5-diones

✍ Kyung-Ho Park; Linda J Cox 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 56 KB

A traceless synthesis of 1,2,4-triazolidine-3,5-diones has been achieved through cyclo-elimination from solid-phase. This traceless cyclo-elimination release step is induced by catalytic amount of base or by simply refluxing the urea carbamate intermediate.

Efficient solid-phase synthesis of 2,3-s

Efficient solid-phase synthesis of 2,3-substituted indoles

✍ Dean A Wacker; Padmaja Kasireddy 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 65 KB

The development of the solid-phase version of the modified Madelung indole synthesis is reported. The chemistry was initiated with the reductive amination of Bal resin using an ortho substituted aniline. The resin bound aniline was acylated with a variety of acid chlorides followed by cyclization wi

Solid phase synthesis of chiral 3-substi

Solid phase synthesis of chiral 3-substituted quinazoline-2,4-diones

✍ Laurent Gouilleux; Jean-Alain Fehrentz; F. Winternitz; Jean Martinez 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 213 KB

Solid-Phase Synthesis of 3,5-Disubstitut

Solid-Phase Synthesis of 3,5-Disubstituted 2,3-Dihydro-1,5-benzothiazepin-4(5 H )-ones

✍ Schwarz, Matthias K.; Tumelty, David; Gallop, Mark A. 📂 Article 📅 1999 🏛 American Chemical Society 🌐 English ⚖ 323 KB

Solid phase synthesis of 3,5-disubstitut

Solid phase synthesis of 3,5-disubstituted oxazolidin-2-ones

✍ S.K. Rastogi; G.K. Srivastava; S.K. Singh; R.K. Grover; R. Roy; B. Kundu 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 140 KB

A versatile method for the solid phase synthesis of oxazolidin-2-ones is described. A resin bound phenolic group was treated with (±)-epichlorohydrin followed by opening of the epoxide ring with sodium azide. The resulting 1-azido-3-aryloxypropan-2-ol was treated with p-nitrophenylchloroformate and