✦ LIBER ✦

Synthesis of (±)-Ambrox from ( E )-Nerolidol and β-Ionone via Allylic Alcohol [2,3] Sigmatropic Rearrangement

✍ Scribed by Barrero, Alejandro F.; Altarejos, Joaquín; Alvarez-Manzaneda, Enrique J.; Ramos, José M.; Salido, Sofía

Book ID: 126159515
Publisher: American Chemical Society
Year: 1996
Tongue: English
Weight: 183 KB
Volume: 61
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo951908o

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of (.+-.)

ChemInform Abstract: Synthesis of (.+-.)-Ambrox from (E)-Nerolidol and β-Ionone via Allylic Alcohol (2,3) Sigmatropic Rearrangement.

✍ A. F. BARRERO; J. ALTAREJOS; E. J. ALVAREZ-MANZANEDA; J. M. RAMOS; S. SALIDO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB

Stereospecific [2,3] sigmatropic rearran

Stereospecific [2,3] sigmatropic rearrangement of allylic sulfoxides and selenoxides. Synthesis of novel polycyclic allylic alcohols and α-hydroxy ketones

✍ Marek Koprowski; Ewa Krawczyk; Aleksandra Skowroñska; Mary McPartlin; Nick Choi; 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 302 KB

Selective Syntheses of Δ α,β and Δ β,γ B

Selective Syntheses of Δ α,β and Δ β,γ Butenolides from Allylic Cyclopropenecarboxylates via Tandem Ring Expansion/[3,3]-Sigmatropic Rearrangements

✍ Xie, Xiaocong; Li, Yi; Fox, Joseph M. 📂 Article 📅 2013 🏛 American Chemical Society 🌐 English ⚖ 586 KB

ChemInform Abstract: Stereospecific [2,3

ChemInform Abstract: Stereospecific [2,3] Sigmatropic Rearrangement of Allylic Sulfoxides and Selenoxides. Synthesis of Novel Polycyclic Allylic Alcohols and α-Hydroxy Ketones.

✍ Marek Koprowski; Ewa Krawczyk; Aleksandra Skowronska; Mary McPartlin; Nick Choi; 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 2 views

ChemInform Abstract: Aryl Sulfoxides fro

ChemInform Abstract: Aryl Sulfoxides from Allyl Sulfoxides via [2,3]-Sigmatropic Rearrangement and Domino Pd-Catalyzed Generation/Arylation of Sulfenate Anions.

✍ Elise Bernoud; Gaetan Le Duc; Xavier Bantreil; Guillaume Prestat; David Madec; G 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views

Synthesis of optically active partly gem

Synthesis of optically active partly gem-difluorinated allylic alcohols via [2,3]-Wittig rearrangements and lipase-catalyzed reaction

✍ Toshiyuki Itoh; Kazutoshi Kudo; Naoko Tanaka; Kohei Sakabe; Yumiko Takagi; Hiros 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 201 KB

2,3]-Wittig rearrangement of 1,1,2-tri¯uoroallylic ethers gave ®ve types of novel 4,4,5-tri¯uoroalk-1,5dien-3-ols. The rearrangement reaction gave the alcohols with perfect (E)\*-selection over the newly created ole®n bond for two substrates. Lipase-catalyzed optical resolution of 4,4,5-tri¯uoroalk-