✦ LIBER ✦

Application of a New Tandem Isomerization−Aldolization Reaction of Allylic Alcohols to the Synthesis of Three Diastereoisomers of (2 R )-1,2- O -Isopropylidene-4-methylpentane-1,2,3,5-tetraol

✍ Scribed by Cuperly, David; Crévisy, Christophe; Grée, René

Book ID: 121338311
Publisher: American Chemical Society
Year: 2003
Tongue: English
Weight: 159 KB
Volume: 68
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo0342727

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1,3-Dipolar Cycloaddition Reactions Lead

1,3-Dipolar Cycloaddition Reactions Leading to the Synthesis of New 2,3,5-Triaryl-4 H ,2,3,3a,5,6,6a-hexahydropyrrolo[3,4- d ]isoxazole-4,6-diones

✍ Kaur, Anjandeep; Singh, Baldev 📂 Article 📅 2014 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 930 KB

Optically pure (S)- and (R)-4,5-dihydro-

Optically pure (S)- and (R)-4,5-dihydro-3H-4-methyldinaphth[2,1-c; 1′,2′-e]azepines. Application to the synthesis of new bidentate ligands with axial asymmetry

✍ Irena G. Stará; Ivo Starý; Jiří Závada 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 317 KB

2,2′-carbonyl-bis(3,5-dioxo-4-methyl-1,2

2,2′-carbonyl-bis(3,5-dioxo-4-methyl-1,2,4-oxadiazolidine): I-A new reagent for the preparation of carbamates and amides, application to the synthesis of dipeptides.

✍ Michel Denarié; Denis Grehouillat; Thierry Malfroot; Jean-Pierre Senet; Gérard S 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 210 KB

2,2'-Carbonyl bis (3,5-dioxo-4-methyl-1,2,4-oxadiazolidine) was prepared and used for the synthesis of various carbamates and dipeptides. 3,5-Dioxo-1,2,4-oxadiazolidines have been found as a part of the natural excitatory aminoacid guisgualic acid and their synthesis has been extensively studied by

A New Resin-Bound Universal Isonitrile f

A New Resin-Bound Universal Isonitrile for the Ugi 4CC Reaction: Preparation and Applications to the Synthesis of 2,5-Diketopiperazines and 1,4-Benzodiazepine-2,5-diones

✍ Kennedy, April L.; Fryer, Andrew M.; Josey, John A. 📂 Article 📅 2002 🏛 American Chemical Society 🌐 English ⚖ 58 KB

A stereospecific synthesis of 3,3-disubs

A stereospecific synthesis of 3,3-disubstituted allylic alcohols. The intermolecular pinacol cross-coupling reaction between .alpha.,.alpha.-disubstituted .alpha.-(diphenylphosphinoyl)acetaldehydes [Ph2P(O)CR1R2CHO] and saturated aldehyde

✍ Park, Jeonghan; Pedersen, Steven F. 📂 Article 📅 1990 🏛 American Chemical Society 🌐 English ⚖ 391 KB

Mitsunobu reaction of 1,5-anhydro-3,4,6-

Mitsunobu reaction of 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-hydroxymethyl-hex-1-enitols and 1,5-anhydro-2-deoxy-4,6-O-protected-hex-1-enitols. A novel method for the synthesis of 2-C-methylene glycosides and an useful alternative to Ferrier rearrangement

✍ Namakkal G. Ramesh; Kalpattu K. Balasubramanian 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 932 KB