✦ LIBER ✦

Transition-Metal-Catalysed Reactions of Diazoesters: Synthesis of Chrysanthemic and Permethric Acid Esters by Cyclopropanation of Conjugated Dienes

✍ Scribed by A. Demonceau; A. F. Noels; A. J. Anciaux; A. J. Hubert; P. Teyssié

Publisher: Wiley (John Wiley & Sons)
Year: 2010
Weight: 182 KB
Volume: 93
Category: Article
ISSN: 0037-9646
DOI: 10.1002/bscb.19840931104

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Transition metal catalysed reactions of

Transition metal catalysed reactions of diazocompounds - part III a one-step synthesis of substituted furanes and esters.

✍ R. Paulissen; E. Hayez; A.J. Hubert; P. Teyssie 📂 Article 📅 1974 🏛 Elsevier Science 🌐 French ⚖ 97 KB

Oxidation of alcohols by transition meta

Oxidation of alcohols by transition metal complexes—iv : The rhodium catalysed synthesis of esters from aldehydes and alcohols

✍ Ronald Grigg; Thomas R.B. Mitchell; Somyote Sutthivaiyakit 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 646 KB

Synthesis of Functionalized Alkenes by T

Synthesis of Functionalized Alkenes by Transition Metal Catalyzed Carbostannylations of Alkynes and Dienes Followed by Cross-Coupling Reactions.

✍ Eiji Shirakawa; Tamejiro Hiyama 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

Cross-Dehydrogenative Coupling Reactions

Cross-Dehydrogenative Coupling Reactions by Transition-Metal and Aminocatalysis for the Synthesis of Amino Acid Derivatives

✍ Jin Xie; Prof. Zhi-Zhen Huang 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 329 KB 👁 2 views

Cross-Dehydrogenative Coupling Reactions

Cross-Dehydrogenative Coupling Reactions by Transition-Metal and Aminocatalysis for the Synthesis of Amino Acid Derivatives

✍ Jin Xie; Prof. Zhi-Zhen Huang 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 364 KB 👁 2 views

Fatty acids, part 20: The base-catalysed

Fatty acids, part 20: The base-catalysed rearrangement of vernolic and other epoxy esters: The partial synthesis of methyl coriolate, methyl dimorphecolate, and some conjugated polyenoic esters by a possible biosynthetic route

✍ H.B.S. Conacher; F.D. Gunstone 📂 Article 📅 1969 🏛 Elsevier Science 🌐 English ⚖ 524 KB

Meth) l ,,ernolate ~s rearranged to methyl cor~olate by hthmna dJeth)lamlde at 0 C Jn about 60 "o y~eld Dehydration of th~s hydroxy ester yields a mixture of octadecatr~enoates By SMlllar reactions hnole~c ester has been con,mrted to racemlc corlohc ester and to racem~c dJmorphecohc ester, and hnole