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Natural Product Synthesis I5 y, M) L9 j3 ~' \$ m/ W
Targets, Methods, Concepts
' v% {7 L( I( l+ [0 z* J% y: D2 _
6 K4 z" B( O2 t, ]' l$ O2 aVolume Editor: Johann H. Mulzer
' T. q; G+ C! O% T. l. Z# }4 f' U1 s5 |& x! S3 G
With contributions by. f6 r# y' [/ C
T. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann
% |3 G: }3 |" _0 }8 XH. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow! J: l7 T9 i+ W: M6 t2 W
A. Spiegel · L.A. Wessjohann; P, `; W1 N2 o: c
, v9 \- B5 V! T7 ~Contents
. A- y& Q; u( h, T1 k8 _Total Syntheses of Kelsoene and Preussin
/ G8 ^# c# H p4 U) Y( tB. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1
1 B9 B& A- t. N1 {( D3 H- kParaconic Acids – The Natural Products from Lichen Symbiont* l+ s! _& K% e5 J% n3 ^% g
R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43
( u& }$ ~" Z/ W/ PRecent Progress in the Total Synthesis of Dolabellane* w( E u6 A& p- |7 t7 Q
and Dolastane Diterpenes
1 `7 L' z/ K2 p, K. w1 @M. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 733 u. t6 e( k6 C) f; n1 s
Strategies for Total and Diversity-Oriented Synthesis
: |5 z! @; a% `of Natural Product(-Like) Macrocycles
7 r0 p% M' F O) K4 QL.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
$ X# l' E( W; _. `Enantioselective Synthesis of C(8)-Hydroxylated Lignans:
9 t2 ]- E, x9 P, R: {4 nEarly Approaches and Recent Advances M. Sefkow . . .. . . . 1852 V0 ~' c. S; l1 p& n) f
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225& q# r: H7 r/ t N6 N' z5 |) }
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237
4 f2 w. U5 M: e1 b' V$ ^# X: D. @% g9 s0 i7 z) `
# u: c0 Z! |! C3 Q0 j. O( B0 j% U; T. i6 s2 [. G
Natural Products Synthesis II
& `7 Q6 D: s3 p+ C$ M HTargets, Methods, Concecpts5 B2 X& Q' R- H" H S! {
6 o/ O* U$ y! l9 BVolume Editor: Johann Mulzer3 c$ U5 v& f. c# ~! n4 m
2 b+ \% m6 u1 A2 B3 ]With contributions by% ]) @0 e+ d6 Q( N# H' a. w
U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·2 t: u/ \ P4 g
J.Mulzer · U.Nubbemeyer · M. Tietze
9 C; f# ~, o, U/ X; w
: v$ z5 K* l) q) N) c s! Q1 H5 P% _! f
Contents) c6 W% `9 h" m% x9 d
Marine Natural Products from Pseudopterogorgia Elisabethae:
2 ~1 a2 |, ]0 e: m9 F4 m- A2 NStructures, Biosynthesis, Pharmacology and Total Synthesis" ]+ W2 ^ }- v( f" r
T. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
3 ?" Q, D0 j0 J/ ERecent Advances in Vinylogous Aldol Reactions and their Applications; Y& r2 s" K# u% [. c+ r
in the Syntheses of Natural Products
" \" `+ J% H7 B3 k1 P: DM.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 431 Q, X% \2 J$ E3 O p9 B0 b6 W
Methanophenazine and Other Natural Biologically Active Phenazines u# u2 \3 H' a( C
U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
, u9 u% t8 u- ]# bOccurrence, Biological Activity, and Convergent Organometallic) B" f) d: _5 _1 P4 F8 g4 n
Synthesis of Carbazole Alkaloids/ x g. u, B% K0 q% G
H.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115 _4 r" }( b/ @3 c: q" m
Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements7 I" d+ b _6 C: ~+ J" S- D: ?
U.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149
% M* s A3 E/ F# W2 z1 WSynthetic Studies on the Pamamycin Macrodiolides* u$ F, l7 k, d8 L1 {! d
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215
" j- r4 z; Y" `; p. s6 N, jAuthor Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
4 e; e* P3 m1 c0 j6 B0 f" PSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2672 w: ~7 s5 k" T: Y: Z. @
1部分共3个压缩卷，解压4.65M，含7个PDF文档
2 ]. L. r; ^% A. Y7 [$ p, |" v6 ^- X2部分共3个压缩卷，解压5.23M，含8个PDF文档
0 Q/ N4 W; b; Y& C1 H. L o0 L: ]2 q5 l# x" H0 i* P" c6 Y. k
[ 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
