✦ LIBER ✦

Synthesis of (2S, 3S, 4R, 5R, 6Z)-2-amino-1,3,4,5-tetrahydroxyoctadecene, a long chain base part of cerebroside

✍ Scribed by Li Yun-Long; Wu Yu-Lin

Publisher: Elsevier Science
Year: 1995
Tongue: French
Weight: 109 KB
Volume: 36
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(95)00738-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of (+)-1,3:2,5-dianhydroviburn

Synthesis of (+)-1,3:2,5-dianhydroviburnitol ((+)-(1R,2R,3S,5R,6S)-4,7-dioxatricyclo[3.2.1.03,6]octan-2-ol)

✍ Claude Le Drian; Pierre Vogel 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 German ⚖ 490 KB 👁 1 views

Asymmetric synthesis of (1R, 2S, 3R)-2-a

Asymmetric synthesis of (1R, 2S, 3R)-2-acetyl-4(5)-(1,2,3,4-tetrahydroxybutyl)imidazole

✍ Matthew D Cliff; Stephen G Pyne 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 192 KB

A new practical synthesis of (2S,3R,4R,5

A new practical synthesis of (2S,3R,4R,5S)-3,4-dihydroxy-2,5-bis(hydroxymethyl)pyrrolidine

✍ Wei Zou; Walter A. Szarek 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 317 KB

Efficient syntheses of 13C-labelled eryt

Efficient syntheses of 13C-labelled erythromycin biosynthetic intermediates. 2: (2S,3S,4S,5R,6R,7R)-3,6,7-trihydroxy-2,4,6-trimethyl[1-13C]nonan-5-olide and S-2-acetylaminoethyl (2R,3S,4S,5R,6S,7R)-3,5,6,7-tetrahydroxy-2,4,6-trimethyl[1-13C]nonanethioate

✍ Katsumi Iida; Masahiro Kajiwara; Mineo Fukui; Tadashi Nakata; Takeshi Oishi 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 French ⚖ 222 KB 👁 1 views

## Abstract The ^13^C‐labelled putative erythromycin biosynthetic intermediates, ((2__S__,3__S__,4__S__,5__R__,6__R__,7__R__)‐3,6,7‐trihydroxy‐2,4,6‐trimethyl[1‐^13^C]nonan‐5‐olide and __S__‐2‐acetylaminoethyl (2__R__,3__S__,4__S__,5__R__,6__S__,7__R__)‐3,5,6,7‐tetrahydroxy‐2,4,6‐trimethyl[1‐^13^C]

Non-Classical Epimerisation of (1S,2S,3S

Non-Classical Epimerisation of (1S,2S,3S,4R,5R)-1-O-Methylcyclohexane-1,2,3,4,5-pentol

✍ Michael Frank; Ralf Miethchen; Helmut Reinke 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 290 KB 👁 1 views

Methoxycyclitol 4 was acetalized in a non-classical one-pot idene moiety was realised in two steps via the corresponding ethylidene acetals 8 and 9; the ethylidene function was procedure with chloral/dicyclohexylcarbodiimide forming the 4-epi derivative 6. The stepwise deprotection of removed with a

ChemInform Abstract: Synthesis of 2-R-6-

ChemInform Abstract: Synthesis of 2-R-6-R′-4-(5-Amino-1,3,4-oxadiazol-2-yl)quinolines.

✍ A. G. Kashaev; A. V. Zimichev 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 21 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