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Natural Product Synthesis I
0 N: ^# W6 O9 ^! u0 H) P- RTargets, Methods, Concepts
! _/ ?( x: r7 G% o2 i, u
- l, N! @% R% i% _/ u2 eVolume Editor: Johann H. Mulzer! N0 ~' ~) @" P. Q, }5 S1 o6 ~* P' S% W
6 {0 t2 |' A5 v# I. G
With contributions by1 P; ~0 C# I4 |3 Z0 N# U" U
T. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann8 @% C2 D {) R+ \0 N. x% y
H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow
$ `, z0 z2 r; u2 }0 p+ q3 F% lA. Spiegel · L.A. Wessjohann
2 o7 P$ F! M5 [9 P" l/ j1 V* ?
7 v6 T' M% N4 g: \/ \0 pContents0 N& m" y, G# Q" E2 n& c) p
Total Syntheses of Kelsoene and Preussin
6 {% `: Q7 `; `" PB. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1( S. g2 a! o+ t5 A: H, h1 w9 E
Paraconic Acids – The Natural Products from Lichen Symbiont
6 V: y: @# I) m& B) S( PR. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43! P( T# J& g2 j2 v' T
Recent Progress in the Total Synthesis of Dolabellane
+ V/ C4 N- ?& o7 y1 ^! [2 Y8 hand Dolastane Diterpenes
8 C3 t U! s2 F; k/ ?5 HM. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
6 k1 P& F/ B" K( \9 K! [% xStrategies for Total and Diversity-Oriented Synthesis
a* M# x5 k7 D: d$ Z& E# Hof Natural Product(-Like) Macrocycles) d; y* ?$ m; R& ~9 I( }4 E
L.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137% h/ h2 `# C, k$ F9 i
Enantioselective Synthesis of C(8)-Hydroxylated Lignans:
& ], y8 k5 A% m) h/ A/ cEarly Approaches and Recent Advances M. Sefkow . . .. . . . 185) r f2 s, e. I& v
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 2252 k: P t' y6 S/ F1 Q
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237. @3 G! h5 i# ~( I0 N
2 P, ~4 a4 t3 u% Z+ O3 z j
) [, s5 p J" z
+ j6 W1 G7 ]- O& VNatural Products Synthesis II
3 u) H2 ~8 ?8 w* A9 u3 CTargets, Methods, Concecpts0 @/ t3 J' R5 L: D: J9 H& g
: Z/ [5 X8 k5 f9 H' i
Volume Editor: Johann Mulzer h7 e" M" K" p ]0 r {0 H
% {( @ E" Z& I" r, F) n( f5 ]With contributions by x x7 S4 G0 q3 w9 B
U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·
9 Z; w8 B) O4 v* W) ?0 V3 o0 T: }J.Mulzer · U.Nubbemeyer · M. Tietze
5 j/ t5 w, E5 i0 P* I5 L7 ~9 c. d0 c' M5 h
$ g* I1 M! t/ l; W$ H2 ^
Contents
8 |/ {0 H8 U! [" z o# E M+ GMarine Natural Products from Pseudopterogorgia Elisabethae:
9 o9 e. J. A( D# sStructures, Biosynthesis, Pharmacology and Total Synthesis0 L4 t/ Y( [+ @$ a$ ?; F1 M+ T
T. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1( S2 E1 f" e2 U% U1 v# Q! w) y" q
Recent Advances in Vinylogous Aldol Reactions and their Applications2 N5 x/ J+ U$ z1 M5 d/ J
in the Syntheses of Natural Products
0 P9 U* e0 V$ C: R" \M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
) ]# @. W# Z6 G. o0 H; JMethanophenazine and Other Natural Biologically Active Phenazines% B) ?+ H* e8 u" C* K
U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77' u* b @+ S, R ` a+ H/ y
Occurrence, Biological Activity, and Convergent Organometallic8 I0 F6 ^# \; i
Synthesis of Carbazole Alkaloids/ o- b, @3 M% a1 l8 A4 V$ r
H.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
$ |- Z, p; u) X! b7 ~3 f& e7 FRecent Advances in Charge-Accelerated Aza-Claisen Rearrangements
0 i& l5 W+ d$ H) _1 GU.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149
9 {3 d3 v* c$ b) l! a2 Q' Z! w( LSynthetic Studies on the Pamamycin Macrodiolides
2 m7 J5 ?* M) \ |6 n. FP.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2153 J0 A4 b+ |; Y: H# b+ D/ W
Author Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
5 T5 r- G9 _4 B8 a" Z/ l. Z4 bSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
! X& @: ^& n" O1部分共3个压缩卷,解压4.65M,含7个PDF文档
' @! v' P& `1 K/ U. z2部分共3个压缩卷,解压5.23M,含8个PDF文档$ R9 H; j& r7 C" B% a
& ^8 M) a+ d. A+ ~[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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