|
|
马上注册，结识高手，享用更多资源，轻松玩转三维网社区。
您需要 登录 才可以下载或查看，没有帐号？注册
x
Natural Product Synthesis I
& s) x( T* `' dTargets, Methods, Concepts6 z8 i( G% `! t5 _1 c1 g3 h" Z! h
! b9 O! E Z7 P$ S8 b0 n
Volume Editor: Johann H. Mulzer$ w8 }4 j0 s9 @$ }/ V E
: r& J1 \ [7 a% T$ Y6 ~With contributions by6 Y; w4 ^( i6 ]1 Q
T. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann4 w1 _3 t9 p3 U$ a$ H6 H
H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow+ `6 c3 p* v- k
A. Spiegel · L.A. Wessjohann# e' i& `. y# C6 v, p
/ J% x, U' W$ \, z7 N1 C, qContents: @/ F2 F' t$ f( d7 X9 V7 n
Total Syntheses of Kelsoene and Preussin! d' x6 ~$ b& `$ e5 o4 Y
B. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 1 r0 Z; v6 g2 @+ p, n7 S. e
Paraconic Acids – The Natural Products from Lichen Symbiont
6 J2 T. C7 ^ a7 G9 t3 v5 \R. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43; ]) P0 K. K8 a) J q! m
Recent Progress in the Total Synthesis of Dolabellane0 o" y! Y2 z9 H, _4 P
and Dolastane Diterpenes
9 ~9 h' v0 E) L; T2 X+ y5 N, s4 h: o1 WM. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 733 k C+ G9 g( X R
Strategies for Total and Diversity-Oriented Synthesis
7 ?9 G, T0 _' Nof Natural Product(-Like) Macrocycles
- O9 c5 B3 m0 I7 KL.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
' L9 W4 x) s( R# G, ]9 ]Enantioselective Synthesis of C(8)-Hydroxylated Lignans:% Z4 |5 l4 l5 V2 u! G
Early Approaches and Recent Advances M. Sefkow . . .. . . . 185' I: O/ ]. {2 q
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225" W" Y5 E+ e# D3 t: H: v
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2375 C2 J! v' o- g& {
# V. s+ b% K0 y& B# J3 L# A
4 S9 a2 d, }+ t- _% T% }
$ `6 e2 T" ^% ~& r. M% H2 b( jNatural Products Synthesis II
3 \! e7 g" ]3 a, j# CTargets, Methods, Concecpts6 l% O, v2 \0 i5 I
+ Y" d( o0 V5 w0 F OVolume Editor: Johann Mulzer0 T m6 T" ]) ?1 o0 n
! B: \5 V; w: w3 X3 t+ m
With contributions by1 G# c0 Y( U9 R& V! c ^8 \/ d" f" D/ U
U. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·
' y9 `3 m; R, U/ YJ.Mulzer · U.Nubbemeyer · M. Tietze( Q$ O2 o" E4 H! W
4 P3 E/ O2 z" n6 I4 J- Q+ u4 _* Q1 x6 ?- P4 r
Contents1 o, w9 @) e% Q9 g2 R3 v
Marine Natural Products from Pseudopterogorgia Elisabethae:, D4 E! {6 v+ P
Structures, Biosynthesis, Pharmacology and Total Synthesis
! o U* j- E( n. v) W2 C2 ]1 cT. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
4 n" M4 h' ?7 S7 lRecent Advances in Vinylogous Aldol Reactions and their Applications9 v( I: I' R. b) c# o, S
in the Syntheses of Natural Products: w/ y% o4 J. O
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
, j% [! X9 v2 I3 fMethanophenazine and Other Natural Biologically Active Phenazines4 G! K8 B4 M% w% i7 N# ~0 V
U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 779 t& G0 Q8 H4 N! n
Occurrence, Biological Activity, and Convergent Organometallic
+ G5 l- j# f: S3 |; [7 GSynthesis of Carbazole Alkaloids
7 l1 ^) K* `: N. l6 g9 V1 OH.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115# Q6 {) b) ?% o
Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements4 D, Q- u* c P6 _( G5 X' j! P
U.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149. |0 T9 P E8 ?) ~
Synthetic Studies on the Pamamycin Macrodiolides6 e+ t5 ^9 N4 O9 w4 K
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215
( h7 N1 w3 a- ~& |: m0 ^/ n' rAuthor Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 251
# F. e; s1 Y$ k( ]Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267) ~; r' J' k' q9 r- H$ h
1部分共3个压缩卷，解压4.65M，含7个PDF文档- Q/ |; X4 H) N( M2 Q0 @
2部分共3个压缩卷，解压5.23M，含8个PDF文档
' I$ w$ S3 z. M$ T* c! d5 y
0 t3 n7 A0 P' \5 o4 }7 T[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
评分
-
查看全部评分
|
[复制链接]
发表于 2008-8-5 18:53:04
