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Natural Product Synthesis I4 w( w! P7 a. w1 B! p
Targets, Methods, Concepts+ |8 t% `3 x5 j( l4 D$ o8 o
$ z0 N, }7 t( I$ v0 D# Q% Q w
Volume Editor: Johann H. Mulzer! ~/ ~8 h) s" d `+ u% n' u& d
% r) v: n5 H" L3 ]With contributions by
1 T" }+ v( G3 F; Y& [- F" P# i/ gT. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann
7 }: m2 L! ]5 b+ C! L4 s. k! [* X SH. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow* W( r: E' ^. Y4 A
A. Spiegel · L.A. Wessjohann
- q$ U$ X1 G$ Q! V Q' z* L3 ~1 E f$ V3 V4 K# _; M
Contents
# N Z0 |/ h* e" R7 PTotal Syntheses of Kelsoene and Preussin, |# Z. I* p+ B$ w
B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1
- u- \$ U/ A! Y! ~# wParaconic Acids – The Natural Products from Lichen Symbiont% ]9 O2 ]# [! {+ b6 q) c
R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43
2 o% T7 _: X5 E7 URecent Progress in the Total Synthesis of Dolabellane8 B: W) w* Y4 t' W; I
and Dolastane Diterpenes
3 _$ F9 o$ \ g( oM. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
7 M1 `% ` l5 c: W& wStrategies for Total and Diversity-Oriented Synthesis' X, j1 g1 a- E, o% {; z* y6 j5 g
of Natural Product(-Like) Macrocycles; g' \" B# P2 l3 `& Z
L.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
* {4 a. P6 K% Q$ l5 c6 F9 c8 t& YEnantioselective Synthesis of C(8)-Hydroxylated Lignans: R5 i) @# M2 e5 S' T+ Q
Early Approaches and Recent Advances M. Sefkow . . .. . . . 185( W( j% [) i* {6 r& K( K" Z4 e3 e
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225
( W; _) g+ N5 w+ M: |# R' ?; x0 cSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237* x2 Y1 ?7 l. B1 @" X/ _& |
0 R9 G/ |- \& Q( O2 c
% {- h. N6 J$ p e5 D* X
+ t& |* b7 ? A9 pNatural Products Synthesis II
5 [6 Y3 o. p6 F+ {Targets, Methods, Concecpts
% ?7 T4 H+ r* W0 \: m. a7 P" G9 K) r" S; _* w( f) K$ u
Volume Editor: Johann Mulzer
; ^4 x! g- ~. T; V7 W7 [: e J: a: y! x
With contributions by) N4 P* v3 ]# N
U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·& ?* Z4 k; W% q. Z
J.Mulzer · U.Nubbemeyer · M. Tietze% ]- [/ I) q0 ^: I
6 _8 @& [+ B6 W" i1 I& ?) r* `
{0 n) @' \! zContents
) m/ f8 P. `3 q* BMarine Natural Products from Pseudopterogorgia Elisabethae:
5 z3 I- Z% ~+ sStructures, Biosynthesis, Pharmacology and Total Synthesis
8 S* \, ` i; ]1 t' M9 F7 XT. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
! d- q9 _1 \3 b3 v+ h, SRecent Advances in Vinylogous Aldol Reactions and their Applications
8 T' S3 q# d+ y! }. K8 W& H7 S2 H# z( Oin the Syntheses of Natural Products; [. ?: N' {# l3 H, d+ _1 n
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
- _" Z8 c/ P. M$ u: `' [Methanophenazine and Other Natural Biologically Active Phenazines& P0 U0 W- n- C9 M {5 u( D
U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
~: H4 M; g1 z& h2 POccurrence, Biological Activity, and Convergent Organometallic
! B, Q* o7 e3 n, X, s; b/ g, A3 {Synthesis of Carbazole Alkaloids
0 J6 D i; w9 _, t% n* X0 YH.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
3 M0 }' T5 u- f: N- b1 nRecent Advances in Charge-Accelerated Aza-Claisen Rearrangements/ {1 [% U$ G; Q. w' o
U.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149- g0 |2 A) o1 f% S$ n W0 i; y
Synthetic Studies on the Pamamycin Macrodiolides C. B) Y O; e. C, g+ l* M
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215
) g+ K9 F3 X, r i! c: R7 qAuthor Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251+ M) x9 B" h6 s: ` b0 H
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
' L4 w) |8 ?+ U/ f3 v5 M1部分共3个压缩卷，解压4.65M，含7个PDF文档
4 `9 e y! `7 y2部分共3个压缩卷，解压5.23M，含8个PDF文档
3 U+ ~' \) w' M- Z# x3 e9 B0 Y% Q! j; _2 W& {- Z. e4 J
[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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发表于 2008-8-5 18:53:04
