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Natural Product Synthesis I: F# w7 d' ~9 n8 S% N/ E
Targets, Methods, Concepts
2 i( ] [* o# }; M4 d4 t, }, F% _) o
Volume Editor: Johann H. Mulzer$ G! F4 Q& n6 l/ Z2 Q( @- V5 ]
4 a) @4 L, N$ Y; d' I9 i, Y) F1 f
With contributions by
" l& f1 ]( ^8 | |/ YT. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann/ k: \# a2 P" d
H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow
3 O& h) c. m. {7 u0 M3 Q: U$ s+ SA. Spiegel · L.A. Wessjohann6 f3 o$ n R& {: N) z
8 f7 L4 S1 h" [, y5 _Contents6 G3 s: T# t( z' V
Total Syntheses of Kelsoene and Preussin: n7 C( f$ s# |" M" w5 @
B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1
7 s3 B: |. [ U- `5 EParaconic Acids – The Natural Products from Lichen Symbiont5 w% S1 j1 q/ T. F! k9 b. d
R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43
6 w, n" A$ T% w T1 K7 X! [6 SRecent Progress in the Total Synthesis of Dolabellane
2 T2 s# k. Z6 E( l+ }and Dolastane Diterpenes e0 ` l T% m4 e+ ~
M. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 730 H" q3 {( r( h$ p9 v9 |/ G
Strategies for Total and Diversity-Oriented Synthesis, `( [+ P" o4 W. I; y3 t
of Natural Product(-Like) Macrocycles7 Q! n& d+ P \7 x# u4 ?
L.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137- |( K% U0 l. d% n. y9 q7 m
Enantioselective Synthesis of C(8)-Hydroxylated Lignans:
1 I4 p. {5 H+ [3 y; v0 WEarly Approaches and Recent Advances M. Sefkow . . .. . . . 1857 E- y: N, J7 o/ _9 x! J
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225" |1 E6 Q/ N( e2 y8 \9 O
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237- ?% U6 l: w# I1 p. F3 I$ j* E
- Q( ?6 U/ P4 ~ {- d3 k0 J, ?
3 P5 h7 C) ^7 R% M. T/ L
: j7 r$ L+ Y$ j, w9 cNatural Products Synthesis II' z) m' t3 _# H, p, h, k+ e- z" g
Targets, Methods, Concecpts
8 s. Z' l( e+ h' p1 ^" p5 M2 z' s' l+ _9 P1 @5 U6 U
Volume Editor: Johann Mulzer7 U) }8 o4 a. \3 ]; ^$ E" y3 ]5 e
( e$ c! n6 L5 P T
With contributions by
. y) G/ l# R; @6 XU. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·6 K% I# f6 ~; d, `1 P- W
J.Mulzer · U.Nubbemeyer · M. Tietze
' s& @$ q) I6 }4 a3 l: W% ? m! O% S/ `# U" e+ O7 J3 B7 \
& P9 }$ [- M" M7 dContents
5 ^, d3 h6 }: T3 y* RMarine Natural Products from Pseudopterogorgia Elisabethae:
t, u+ m9 H3 e+ V$ cStructures, Biosynthesis, Pharmacology and Total Synthesis
3 @; K* [) j5 I3 h! vT. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 n2 o# H. U7 {& W! G5 k
Recent Advances in Vinylogous Aldol Reactions and their Applications
$ _/ H+ s2 J: d' O# v3 Xin the Syntheses of Natural Products: ?$ l2 Z: V9 `7 H
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43% G+ Y' B; q) e$ V# A; S
Methanophenazine and Other Natural Biologically Active Phenazines
6 P, h; U7 U/ D3 qU. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 778 G [3 U2 d* a/ B2 I, v
Occurrence, Biological Activity, and Convergent Organometallic
8 H# U0 T. `+ [' U8 TSynthesis of Carbazole Alkaloids
6 _% q( Z0 \) [H.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115" b) V. [* f) U& v. b" C# r" q
Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements: C9 Z, T7 J! `, U8 D% \. ?
U.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149& v/ L; M& S# a& c1 _1 Y: x7 W
Synthetic Studies on the Pamamycin Macrodiolides' h' }- T" T* @- P) x$ y1 e
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2154 Y) Z, P9 u4 u- q& l) [2 I- \
Author Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
3 n) k9 d+ B- cSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
! H0 {) u0 m7 Y+ P1部分共3个压缩卷,解压4.65M,含7个PDF文档+ V4 n3 K# `4 {2 \
2部分共3个压缩卷,解压5.23M,含8个PDF文档
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/ ], h l/ ] C, h6 \[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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