๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Investigation into the Absolute Stereochemistry of the Marine Sponge Alkaloid Pyrinodemin A.

โœ Scribed by Stuart P. Romeril; Victor Lee; Jack E. Baldwin; Timothy D. W. Claridge; Barbara Odell

Publisher
John Wiley and Sons
Year
2004
Weight
66 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

โœฆ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

๐Ÿ“œ SIMILAR VOLUMES

Synthesis of Topsentin-A, A Bisindole Al
Synthesis of Topsentin-A, A Bisindole Alkaloid of the Marine Sponge Topsentia genitrix
โœ J. C. Braekman; D. Daloze; C. Stoller ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› Wiley (John Wiley & Sons) โš– 153 KB ๐Ÿ‘ 1 views

ring sponge TOp8mtM g e n i t r k , has been achieved starting from 3-acetylindole. The synthesis of topsentin-A, a bisindole alkaloid isolated from the ma-Recently, we reported the isolation from the marine sponge T o p e e n t i a g e n i t r k of three related basic compounds, topsentin-AU), -el

The Absolute Configuration of Axinellami
The Absolute Configuration of Axinellamine A, a Pyrrole Alkaloid of the Marine Sponge Axinella sp., was Determined as R by Synthesizing Its (S)-Isomer
โœ Masanori Seki; Kenji Mori ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 247 KB ๐Ÿ‘ 1 views

Scheme 2. Synthesis of the achiral building block 7; reagents: (a) ICH 2 CO 2 Et, FeSO 4 โ€ข7H 2 O, H 2 O 2 , DMSO (72%); (b) (Boc) 2 O, DMAP, MeCN (93%); (c) DIBAL, CH 2 Cl 2 ; (d) (EtO) 2 P(O)CH 2 -CO 2 Et, NaH, THF (63% based on 3); (e) MnO 2 , CHCl 3 Scheme 3. Synthesis of (S)-axinellamine A (1);