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Natural Product Synthesis I
# a4 P0 s6 J' U# e: w' u, C, ^Targets, Methods, Concepts: T5 D$ u1 H9 U9 H8 Z
& m% ]+ R( Q! s% W& kVolume Editor: Johann H. Mulzer
+ ^. S5 ^9 q" q* D" U+ ]- N; G1 i" b: e! ]$ `0 k1 J0 \
With contributions by
3 P% _5 H) |' fT. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann
$ F ~& R8 N: F, LH. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow
2 {' h+ y5 l* u6 ?# _1 \0 Z# K: YA. Spiegel · L.A. Wessjohann
* E: G7 i, u8 J* J/ S
" H& j- o, A+ {5 ?% [Contents
. }. m# I+ K$ u9 N$ n* Q% KTotal Syntheses of Kelsoene and Preussin- f8 {8 r0 G. w2 k4 u
B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1
: `- A7 V% Q( J* k" @3 R8 fParaconic Acids – The Natural Products from Lichen Symbiont9 x0 G. l6 v" h' e
R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 434 V. S2 I5 T# p
Recent Progress in the Total Synthesis of Dolabellane
& x) Z0 q# s! k* Uand Dolastane Diterpenes
- _& b0 j2 \# E5 dM. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
. V* d. z3 h" F' ~* c8 uStrategies for Total and Diversity-Oriented Synthesis
" x: J# \# M# }* T% ~+ i, nof Natural Product(-Like) Macrocycles. n; s6 y) |+ m8 r" O
L.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
' l. M) }/ [3 p% C% s& _' tEnantioselective Synthesis of C(8)-Hydroxylated Lignans:* S1 D, M" v; c- M1 B
Early Approaches and Recent Advances M. Sefkow . . .. . . . 185. H! Y; Q5 Q# w3 z
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225
9 m P% r* |- I' ^; u: t3 Z9 x: lSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237- m1 c8 D. v. c
, {6 q- q$ s- V# ~$ C) o: ?7 M9 H3 r
* B+ x9 U' k" ^5 o( @# t0 k' g
Natural Products Synthesis II; y) v" V3 w0 Q! U) h
Targets, Methods, Concecpts5 n% Y. c" J. ~6 O9 K, N/ R. @
. S! U' E, l0 t' I/ P6 [Volume Editor: Johann Mulzer
7 s3 m% t' m: ]9 {: @$ ]3 _' H. s+ d: ^! ?+ p
With contributions by
" B9 G& u: j; E7 gU. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·+ B3 f% A+ h, v8 `
J.Mulzer · U.Nubbemeyer · M. Tietze( b d+ \( ]2 r6 n' |9 X
1 @9 W8 J; T, U4 C! g w( x8 M' S( `
Contents
: j3 M4 h2 u# U5 ^- h9 |: P" B! e2 d$ sMarine Natural Products from Pseudopterogorgia Elisabethae:
9 t' D" I9 T0 [' iStructures, Biosynthesis, Pharmacology and Total Synthesis
2 M! k% A* `- a5 a. {T. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 B) I; k' w1 ^. p
Recent Advances in Vinylogous Aldol Reactions and their Applications2 _, K8 |/ R% w" @- `2 k
in the Syntheses of Natural Products2 I+ Q8 V* N. T* D, ]7 R% P) k
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43, @; V2 t6 R2 Z# p2 S f
Methanophenazine and Other Natural Biologically Active Phenazines
8 }+ R' y+ M2 T" m" m3 T% \U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
$ P$ f! [- F: d( p0 A+ |" \, e% lOccurrence, Biological Activity, and Convergent Organometallic3 f8 I* ] c x' F: ]- @
Synthesis of Carbazole Alkaloids4 B0 k6 M. |# X! J( ~
H.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1155 s- E, ~- j$ G9 E9 v
Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements
! P6 d$ x5 n" VU.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149
- [$ A& J1 v1 d- h5 N, M8 l( _# ]/ l5 tSynthetic Studies on the Pamamycin Macrodiolides/ k5 v, b& {) x k- L
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2156 }3 h$ X; ?" d# a' ^- _
Author Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
5 R D8 ^( H1 h$ |0 I! P& HSubject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
$ F9 e' z- W8 I) t0 {( H. G) c1部分共3个压缩卷,解压4.65M,含7个PDF文档
5 _, n9 E& g u2部分共3个压缩卷,解压5.23M,含8个PDF文档3 z8 U5 j, b9 y/ q
4 p8 P5 |; ~9 y, D, h. N# x* t2 R
[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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