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Natural Product Synthesis I7 Z3 B- \( I: c/ `, E* P8 i1 ]+ Q
Targets, Methods, Concepts0 _9 u# r! [. c: f
- X5 `+ t: y4 Q% `Volume Editor: Johann H. Mulzer7 e( j7 m& R4 x
" M6 P8 A2 C- h J! R$ `& [( v
With contributions by
. }1 c' J: z- _8 f2 p3 |! @; OT. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann+ f1 L+ F- n! Z( y9 [; y1 @- X
H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow" d2 z9 \) `+ U0 x/ y! h1 p( x# |
A. Spiegel · L.A. Wessjohann
6 n6 o7 }- ?- R# Q; t/ m' g# J' ~1 S6 h3 }
Contents
% I3 s* R9 t- h4 w( k) s `Total Syntheses of Kelsoene and Preussin
. P; P6 J% e m4 `B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1( [3 `; |. S' j' v; J" n; n) d
Paraconic Acids – The Natural Products from Lichen Symbiont" ` |9 i& j w# f# W+ U- C7 m. E& B
R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43' a5 g/ D2 w6 R5 a4 X @
Recent Progress in the Total Synthesis of Dolabellane. g6 A" [+ [+ Y6 m4 U0 h
and Dolastane Diterpenes
8 }: Y v: r! _6 E1 fM. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 738 R" M) w* S o
Strategies for Total and Diversity-Oriented Synthesis5 ?3 ]4 g" D) G7 t8 i$ }* O( I
of Natural Product(-Like) Macrocycles
+ R5 `. h" s# ~1 E$ X! T* OL.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 1378 N5 W* a3 d( \0 Y& m8 }* `8 `
Enantioselective Synthesis of C(8)-Hydroxylated Lignans:! R& P- Z1 h, s0 P- _3 L: J
Early Approaches and Recent Advances M. Sefkow . . .. . . . 185
^% Y" w8 T7 u0 L, ]$ hAuthor Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225
! Q, m) U( o- e# bSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237% k/ K% V: }* @6 a3 L
0 ? b; y+ p, F" H2 s' ]4 R" [5 w6 |/ S5 D' E+ V8 J N
: B% }+ j) k8 sNatural Products Synthesis II
* L3 K2 ]1 y7 X# R9 E$ w* ITargets, Methods, Concecpts
& z' n( w2 J+ m1 v: h3 s( p( a5 E7 }( U
Volume Editor: Johann Mulzer. r( x8 f! x1 Q( o# V% N" Z
. s+ @% V2 k& a
With contributions by3 z6 u9 }- L q" A
U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·- o9 w8 H* Y- ^% ~
J.Mulzer · U.Nubbemeyer · M. Tietze/ H) k) A8 z& j6 J* K9 F% `! Z
& G1 |$ u' o$ x V2 F* k" V! n. u, I, M% I
Contents
8 C( D" ~; y( f7 A6 sMarine Natural Products from Pseudopterogorgia Elisabethae:
! X, u& r/ n0 t) u) IStructures, Biosynthesis, Pharmacology and Total Synthesis
8 l( l$ C& Y4 s3 k* oT. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
$ L: P/ I0 L- K- E) nRecent Advances in Vinylogous Aldol Reactions and their Applications
) k2 _. r S. N& i* r$ A* u: Vin the Syntheses of Natural Products% Y0 ~! m: `) Y1 w6 r4 A( _. Y0 H: }
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
( J8 u7 @9 @& N2 H" TMethanophenazine and Other Natural Biologically Active Phenazines
7 g7 I/ ]1 @5 `9 I( f+ NU. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
3 D9 X) f! j! h) rOccurrence, Biological Activity, and Convergent Organometallic
; n) f. M% m: m- c0 e6 tSynthesis of Carbazole Alkaloids( J( h6 W9 p+ L# \: @8 ~+ a
H.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
( J3 C1 t+ a3 x1 {- x& s2 kRecent Advances in Charge-Accelerated Aza-Claisen Rearrangements
" m6 r; l# ^- F9 L1 d4 }+ VU.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149
/ H* n9 e3 s/ s7 f% n2 ^Synthetic Studies on the Pamamycin Macrodiolides3 ~4 w V6 l# y9 B. X3 M) t- y% [
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215
?/ ]% a. _- S) xAuthor Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
# {' ?8 k3 D. ^3 i7 p; LSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2678 \) q* [5 o$ u4 R
1部分共3个压缩卷,解压4.65M,含7个PDF文档# j& H9 j4 f# g" u/ E+ [
2部分共3个压缩卷,解压5.23M,含8个PDF文档
& `( O: U9 g; i. b$ |4 \
$ ] z" @/ Y( Q4 J/ ^; X[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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