✦ LIBER ✦

Synthesis of (4R,5R)-muricatacin and its (4R,5S)-analog by sequential use of the photo-induced rearrangement of epoxy diazomethyl ketones

✍ Scribed by Marcel P.M. van Aar; Lambertus Thijs; Binne Zwanenburg

Book ID: 103400550
Publisher: Elsevier Science
Year: 1995
Tongue: French
Weight: 832 KB
Volume: 51
Category: Article
ISSN: 0040-4020
DOI: 10.1016/0040-4020(95)00670-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of (4R,5R

ChemInform Abstract: Synthesis of (4R,5R)-Muricatacin and Its (4R,5S)-Analogue by Sequential Use of the Photo-Induced Rearrangement of Epoxy Diazomethyl Ketones.

✍ M. P. M. VAN AAR; L. THIJS; B. ZWANENBURG 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB

Synthesis of (2S,4R,5R)-4,5,6-Trihydroxy

Synthesis of (2S,4R,5R)-4,5,6-Trihydroxynorleucine and 5-Hydroxynorvaline from precursors obtained by an unusual rearrangement in a 5,6-dihydro-2-pyrone

✍ Alejandro P. Nin; Rosa M. de Lederkremer; Oscar Varela 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 547 KB

ChemInform Abstract: Synthesis of (2S,4R

ChemInform Abstract: Synthesis of (2S,4R,5R)-4,5,6-Trihydroxynorleucine and 5- Hydroxynorvaline from Precursors Obtained by an Unusual Rearrangement in a 5,6-Dihydro-2-pyrone.

✍ A. P. NIN; R. M. DE LEDERKREMER; O. VARELA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A Versatile Approach Towards Enantiopure

A Versatile Approach Towards Enantiopure α-Methyl β-Hydroxy Ketones. Application to the Synthesis of (4R,5S) Sitophilure and of Its Stereoisomers

✍ Delas, Christophe; Szymoniak, Jan; Thery, Nadine; Moïse, Claude 📂 Article 📅 1998 🏛 Taylor and Francis Group 🌐 English ⚖ 287 KB

Pheromone Synthesis, CXXXV. Synthesis of

Pheromone Synthesis, CXXXV. Synthesis of (4R,5R,6S,7E,9E)-4,6,8-Trimethyl-7,9-undecadien-5-ol and Its Antipode, the Female Specific Compound of the WoodroachCryptocercus punctulatus

✍ Mori, Kenji ;Itou, Masamichi 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 674 KB

## Abstract (4__R__,5__R__,6__S__,7__E__,9__E__)‐4,6,8‐Trimethyl‐7,9‐undecadien‐5‐ol (1) and its antipode 1′, the female specific compound of the woodroach __Cryptocercus punctulatus__, were synthesized by starting from methyl (__R__)‐3‐hydroxy‐2‐methylpropanoate (C).

ChemInform Abstract: Lipase-Mediated Syn

ChemInform Abstract: Lipase-Mediated Synthesis of the Enantiomeric Forms of 4,5-Epoxy-4,5-dihydro-α-ionone and 5,6-Epoxy-5,6-dihydro-β-ionone. A New Direct Access to Enantiopure (R)- and (S)-α-Ionone.

✍ Josefina Aleu; Elisabetta Brenna; Claudio Fuganti; Stefano Serra 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

Lipase-Mediated Synthesis of the Enantiomeric Forms of 4,5-Epoxy-4,5-dihydro-α-ionone and 5,6-Epoxy-5,6-dihydro-β-ionone. A New Direct Access to Enantiopure (R)-and (S)-α-Ionone. -In continuation of a recent study a lipase-mediated approach to optically active α-ionone starting from its racemate is