✦ LIBER ✦

Enantiocontrolled synthesis of (4S,5S,6S)-6-benzyl-4,5-epoxy-6-hydroxy-2-cyclohexen-1-one, a model compound for the epoxycyclohexenone moiety of scyphostatin

✍ Scribed by Takashi Izuhara; Tadashi Katoh

Publisher: Elsevier Science
Year: 2000
Tongue: French
Weight: 97 KB
Volume: 41
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)01312-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Enantiocontrolled S

ChemInform Abstract: Enantiocontrolled Synthesis of (4S,5S,6S)-6-Benzyl-4,5-epoxy-6-hydroxy-2-cyclohexen-1-one (I), a Model Compound for the Epoxycyclohexenone Moiety of Scyphostatin.

✍ Takashi Izuhara; Tadashi Katoh 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 25 KB 👁 1 views

Concise asymmetric synthesis of a model

Concise asymmetric synthesis of a model compound, (4S,5S,6S)-6-(2,2-dimethoxy)ethyl-4,5-epoxy-6-hydroxy-2-cyclohexenone, for the cyclohexenone core of scyphostatin

✍ Hiromichi Fujioka; Naoyuki Kotoku; Yoshinari Sawama; Yasushi Nagatomi; Yasuyuki 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 90 KB

Synthesis of (1S,5S)-4,5-Dihydro-1,5-epo

Synthesis of (1S,5S)-4,5-Dihydro-1,5-epoxy-1H-2-benzoxocin-6(3H)-one from (S)-Malic Acid Derivatives

✍ Wünsch, Bernhard ;Diekmann, Heike 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 997 KB

## Abstract The homochiral 1,3‐dioxanes 8a–e with a 2‐bromophenyl substituent in position 2 and an electrophilic group in position 4 were stereo‐ and regioselectively prepared from the (__S__)‐malic acid derivatives 6a, 6b, 11, and 14. Attempts to prepare the tricycles 5a–c by connecting the 2‐phen

Stereoselective synthesis of N-Boc-O-ben

Stereoselective synthesis of N-Boc-O-benzyl-(4S,5S)-5-amino-4-hydroxy-6-phenylhexanoic acid, the hydroxyethylene isosteric moiety of potent HIV-1 protease inhibitor

✍ Tk Chakraborty; Kiran Kumar Gangakhedkar 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 152 KB

N-Boc-O-benzyl-(4S,5S)-5-amino-4-hydroxy-6-phenylhexanoic acid is synthesized in a highly stereoselective way involving, as a key step, regioselective opening of carbohydrate-based aziridine ring.

S5N6(CH2)4—The First Spirocyclic 1′λ6-Th

S5N6(CH2)4—The First Spirocyclic 1′λ6-Thiacyclopentane Derivative of a Sulfur-Nitrogen Compound

✍ Prof. Dr. Herbert W. Roesky; Dipl.-Chem. Cornelia Graf; Dr. M. N. S. Rao; Prof. 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 243 KB 👁 1 views

A practical method for multigram scale s

A practical method for multigram scale synthesis of (+)-methyl 5(S),6(R)-epoxy-6-formylhexanoate and 2(R),3(S)-epoxyoctanal, key intermediates for synthesis of leukotrienes A4

✍ Yuichi Kobayashi; Yasunori Kitano; Takashi Matsumoto; Fumie Sato 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 212 KB

A practical method for multigram scale synthesis of (+)-methyl 5(S),6(R)-epoxy-6-formylhexanoate (l\_) and 2(R),3(S)-epoxyoctanal (z), key