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Natural Product Synthesis I/ ]* R. g+ i% B& X
Targets, Methods, Concepts
3 q, I0 D9 z. y( v+ @1 @- Q' v6 H9 v
Volume Editor: Johann H. Mulzer
# N' ?7 ]2 b) M8 m( m7 I( @
! x9 o% C" B/ I cWith contributions by: J! I% M' d' X
T. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann
8 S( ]8 w! t! |H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow
6 n; k" F# {" y7 {3 \! [& ZA. Spiegel · L.A. Wessjohann7 D. R7 P% T5 B8 O3 a3 Z
$ a6 d, J6 v4 bContents) T6 |) \6 O" M9 X4 a
Total Syntheses of Kelsoene and Preussin, Z1 C( R9 K2 l4 q1 M6 x
B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1
! r8 x9 x2 R# J1 ]0 oParaconic Acids – The Natural Products from Lichen Symbiont
, R' ?" H4 S3 G% a8 o! E$ GR. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43
* h$ B g' I& f( X* l. [Recent Progress in the Total Synthesis of Dolabellane. i% R1 R6 [' j3 Q! {0 W
and Dolastane Diterpenes4 t+ J7 h% K1 }7 O8 `- f
M. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
. [" Z8 D* o9 v# G6 MStrategies for Total and Diversity-Oriented Synthesis& _0 ^3 |$ a9 ]0 Y5 i" M, X
of Natural Product(-Like) Macrocycles; u3 D& f* C0 d; x5 n. @+ |& k
L.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137: m3 d0 {! e) @' H) p7 O5 p* e% T
Enantioselective Synthesis of C(8)-Hydroxylated Lignans:
0 t* h, H3 k5 d4 X: K) w3 f$ q& y/ }Early Approaches and Recent Advances M. Sefkow . . .. . . . 185
( c* F( a2 h5 qAuthor Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225: U# [0 _9 t1 f. R; m( b
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2379 j8 u4 L' E; R
9 k4 q+ [7 G( ~% h& E
1 Y( O# d _4 j/ v3 q- C0 F$ ?: m
Natural Products Synthesis II" Q5 F6 }! s9 f8 r. a& I
Targets, Methods, Concecpts
& g. T9 U$ {; f- \: l* A7 w* o: l; d& V; s8 u+ b# d+ f
Volume Editor: Johann Mulzer0 i N' ~; h' o, w, E
+ M+ A0 l9 p8 y8 [+ h0 n. H3 z# S6 tWith contributions by
4 a: r) X( Z* j" @* BU. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·
1 u8 b! O, d7 ]8 vJ.Mulzer · U.Nubbemeyer · M. Tietze! T# h3 a' T0 n) q# u
7 e: ~4 P' m# r1 n& O h5 c5 E1 g
- m- Z4 @' Z: k; W! ?2 ]9 dContents
1 j6 K* u7 x& \7 y. |; C$ PMarine Natural Products from Pseudopterogorgia Elisabethae:9 X) v3 m7 D% J. e2 y
Structures, Biosynthesis, Pharmacology and Total Synthesis
! l2 R: s5 [6 r5 ?$ M0 S; D- {* F- E, ^T. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
7 A5 Q/ r* X8 f* L4 E; MRecent Advances in Vinylogous Aldol Reactions and their Applications8 M' ~2 t1 R" b; v! Q& |: k
in the Syntheses of Natural Products3 e5 D6 M2 ?5 h) T
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
/ l: t! l! O+ B4 o9 w5 w: U0 @Methanophenazine and Other Natural Biologically Active Phenazines
- a$ ?& ?# u5 f* OU. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
( D% ^5 b( u, ~# _8 C- M& eOccurrence, Biological Activity, and Convergent Organometallic' N8 e6 V" B+ ~0 ]0 _; d8 r, u& J
Synthesis of Carbazole Alkaloids
! u. Y6 x+ o, i5 {; sH.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115; R7 N) C/ B) }9 n8 O! d. ?3 q! ]
Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements
' [3 D# v x# l. s1 ]" @U.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149- `1 h3 E1 K" @" Z' u( N
Synthetic Studies on the Pamamycin Macrodiolides
! v. {5 F; }- H T& R* J$ FP.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215. ?' J6 V i9 b( y
Author Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
! m- h( ]$ y" v& l' p2 m+ [3 HSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
9 U. K9 w7 D' J! l1部分共3个压缩卷，解压4.65M，含7个PDF文档
- x, e! f6 `3 X& r2部分共3个压缩卷，解压5.23M，含8个PDF文档/ j" \( T0 D* v, _% _: Q
. L$ D. b5 C& x- j* Y$ ?
[ 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
