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Natural Product Synthesis I# X! p+ _3 E, S2 R. ?3 r
Targets, Methods, Concepts' K" P; m- o2 Y% l8 p# N
$ n& f, B; S6 H! Q' B# IVolume Editor: Johann H. Mulzer
/ b' h4 J4 s1 @, O
0 Q( b3 d3 T* x- e6 K+ J) RWith contributions by
' y. s2 h K/ [3 n: ST. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann- F9 i1 I( g9 L9 _- R
H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow
& P5 o* z2 C* B ~/ [A. Spiegel · L.A. Wessjohann
4 @8 A- s' d5 \# c" o$ G; ]8 ~' }8 F& L, Y$ y: k/ y
Contents) y: f& b/ U2 i, q6 [' @& H
Total Syntheses of Kelsoene and Preussin
* S8 p& C/ y& y, W( a# A( }, vB. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1
5 q" F# ~* d. w1 y( `' @Paraconic Acids – The Natural Products from Lichen Symbiont1 R' s" y" {! d
R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43
) L! [# X* o z1 y) dRecent Progress in the Total Synthesis of Dolabellane \' ?8 I# F# F
and Dolastane Diterpenes9 C: u; d0 G- W. q
M. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 73# `0 O( m ?; R4 X$ Y3 n; f
Strategies for Total and Diversity-Oriented Synthesis7 v9 K! d( ]* m7 a' i3 J
of Natural Product(-Like) Macrocycles
' I1 K+ \5 e! kL.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
( y1 N( e- H) w5 sEnantioselective Synthesis of C(8)-Hydroxylated Lignans:
' T' q9 O, k6 n: }( J: SEarly Approaches and Recent Advances M. Sefkow . . .. . . . 1854 Q1 Y% Y& [, z( {9 ]5 y& e' v2 c
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225
% u* n- F, {7 WSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237
% y U9 J7 [% y) i% J" x7 V% h9 Z8 q4 U1 R
; J, n2 r* j( q# R- `
; I0 `% o l# P, p' L) @# C' K
Natural Products Synthesis II. C+ _. t; U7 G G
Targets, Methods, Concecpts
4 x. U/ ?2 }/ S7 o
& X2 n: e1 F6 q8 V& O3 N, GVolume Editor: Johann Mulzer, u6 |, H$ V- H+ |3 w: N2 T
! @% }+ y6 Z; d6 m4 T& y2 }With contributions by
; ~6 X2 V4 a* S! r3 w! ~U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·' ^, ~; i; N) Z1 B6 Y8 O4 y9 ^0 w
J.Mulzer · U.Nubbemeyer · M. Tietze; s. \3 @; L$ H' Z( J( z2 m ]
2 y* @' x- f: _# C" l
3 U8 E' X( j4 Q3 b' q$ L# G! jContents
- o8 [! z- W' z0 WMarine Natural Products from Pseudopterogorgia Elisabethae:, f R3 }+ E' d( p2 D: b
Structures, Biosynthesis, Pharmacology and Total Synthesis
- I& M% v! N2 ^$ V. Y, ?% xT. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
) X: k1 q2 g! l) ~Recent Advances in Vinylogous Aldol Reactions and their Applications
0 z7 @( r' Q( M& \$ k& n% P: pin the Syntheses of Natural Products; E: L' _0 {: d5 `9 ]
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43, M# S7 q( T4 e
Methanophenazine and Other Natural Biologically Active Phenazines
, E+ T r- N! p! r5 `U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77( M$ R6 N+ Q, {% K" X. c% u
Occurrence, Biological Activity, and Convergent Organometallic
" h8 m& W8 E" V' K- K3 r3 QSynthesis of Carbazole Alkaloids
$ `3 M, y* |$ R" R/ |0 y1 b6 tH.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
7 _: Q7 o# F6 u# c4 WRecent Advances in Charge-Accelerated Aza-Claisen Rearrangements- U/ z I' M. M6 L: Y* a
U.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149
1 Y1 I3 V) Y! t4 }9 RSynthetic Studies on the Pamamycin Macrodiolides. S" P$ r: R( B; r2 r6 l* O
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215
) l" M7 `! N! s2 Q. N" ^5 r; nAuthor Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
8 `# f( H2 T& S( KSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
2 {2 c& |- M1 t" W+ X' w/ {) D1部分共3个压缩卷,解压4.65M,含7个PDF文档
N0 W4 M2 c: ~1 K4 q5 J. @2部分共3个压缩卷,解压5.23M,含8个PDF文档% F) x- u" C Y) _, N
) n3 k' Q! q2 c8 P[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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