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Natural Product Synthesis I
0 i: Y. s5 {7 e' N9 YTargets, Methods, Concepts
" B) Z! }! i" `* l9 |/ E" M1 S4 X H- ?& f* p4 M2 {' y5 V) _
Volume Editor: Johann H. Mulzer$ E) T5 P1 T: A2 k& o
$ A/ t* v4 E3 eWith contributions by+ q& B7 f8 \. h3 r
T. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann
+ s, E- u% w) J7 H; D+ GH. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow6 Q# x7 R- e: `3 k( l
A. Spiegel · L.A. Wessjohann
# v& g& C. F4 Y/ X9 d+ W5 a. Z# }- `9 L% K' G# i
Contents
( Q; A0 l; E4 s [* ~/ }! VTotal Syntheses of Kelsoene and Preussin' k& M& ]( k- }$ o# l) X
B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1& f8 [' j5 [7 T* r0 r* `
Paraconic Acids – The Natural Products from Lichen Symbiont
/ p! w0 a. f& U/ |R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43. K T/ o, h) l6 i8 d0 ]
Recent Progress in the Total Synthesis of Dolabellane
+ F V1 p8 a4 _ S9 mand Dolastane Diterpenes
1 j' x9 a) S* v& |M. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 73$ q( X9 N6 _" i4 ^4 L0 T
Strategies for Total and Diversity-Oriented Synthesis
, C8 m- ` e0 |6 H' `' B; ]5 \of Natural Product(-Like) Macrocycles% y* z9 w0 z i& m2 X. K; B
L.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
$ \' b- e9 d8 a9 W# x; |, iEnantioselective Synthesis of C(8)-Hydroxylated Lignans:: E9 Y! l! l" V$ _/ Y
Early Approaches and Recent Advances M. Sefkow . . .. . . . 185
# T1 |# V' v2 S: Y @Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225
+ k/ v2 E+ n# bSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237
, Q' v& m, y4 T" P4 I- s7 t
- k2 I% ^7 m. C. U0 [# W0 P' ^
; N2 f s" e$ n
1 D+ D$ r# R3 L9 z: }, `Natural Products Synthesis II0 `4 W" w2 R2 C
Targets, Methods, Concecpts
; p$ w: N' O5 }4 u; U
4 ^" g4 D: w7 u B4 L ~Volume Editor: Johann Mulzer
& k/ u6 d; V3 i( X, W9 K6 q8 u+ q4 d0 b2 D" O- u) k6 p0 U
With contributions by1 j! }6 A2 M; b5 M# N
U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·1 G/ X q8 z/ _& A( h
J.Mulzer · U.Nubbemeyer · M. Tietze
, ^# T. z# s0 Y) m& ~. S; o
& M% I; ? K" x! ]
( g* d8 \* F( a8 w# L) CContents8 L6 f, I! P/ Z5 z1 r
Marine Natural Products from Pseudopterogorgia Elisabethae:
. `/ I6 F6 m- `6 _8 d6 {0 [ {Structures, Biosynthesis, Pharmacology and Total Synthesis
) w$ d$ w" |+ ^ TT. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
. k4 o( W) c* J n1 E9 JRecent Advances in Vinylogous Aldol Reactions and their Applications5 P& Z! r+ F- w
in the Syntheses of Natural Products
7 f$ f/ D# \- r4 `: l( C0 d* x" cM.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
+ |% z! {- n5 x! }Methanophenazine and Other Natural Biologically Active Phenazines
! v: I# Y: R$ M0 k1 aU. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
& L7 b6 t) _: @: t/ D% w- U0 XOccurrence, Biological Activity, and Convergent Organometallic2 p0 d& \# a& z$ V- _* B; u$ W
Synthesis of Carbazole Alkaloids
8 ?* Z( W) Y4 a' M; VH.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
% i8 F3 R. L$ w% f6 iRecent Advances in Charge-Accelerated Aza-Claisen Rearrangements
7 @! g5 b) a3 o1 f! rU.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1492 v% s! a- H6 i" B- D$ L. N
Synthetic Studies on the Pamamycin Macrodiolides/ }5 g( Y% D0 r
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215" {% H3 L. T+ j& t
Author Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
. ]# m7 A' X! zSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
, N( y( q( _4 P1部分共3个压缩卷，解压4.65M，含7个PDF文档
- t0 Z# ^) n) _2部分共3个压缩卷，解压5.23M，含8个PDF文档* t1 i: |( {1 ~% w8 V l& i
9 K) d( X+ | K. o[ 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
