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Natural Product Synthesis I4 e7 B9 G5 K( k
Targets, Methods, Concepts* L& p2 {+ l7 b& @2 L: p T- y5 h% |+ A
9 u0 w" t6 S1 P2 e- TVolume Editor: Johann H. Mulzer0 G9 ~" c: @8 \/ c* { n3 A8 T
: p5 P3 g( ^: I) P! _: m
With contributions by
7 N, |0 Q0 s( g/ `; E$ @1 uT. Bach · R. Bandichhor · B. Basler · S. Brandes · M. Hiersemann Y0 y" g( p) H4 F+ u' E8 y
H. Helmboldt · B. Nosse · O. Reiser · E. Ruijter · M. Sefkow
. C0 c0 g& t/ o; p+ d/ `0 qA. Spiegel · L.A. Wessjohann
+ O6 x% M6 v0 a \; Y5 k
& K) e) v" L; u8 E& z5 NContents
/ p# O8 X9 H" N$ I0 w6 |Total Syntheses of Kelsoene and Preussin
/ v3 z1 R! B. f% N% J0 y+ D1 rB. Basler · S. Brandes · A. Spiegel · T. Bach . . . . . . . . . . . . . . . . . . . 15 H W- h( p# [8 R/ ?0 A
Paraconic Acids – The Natural Products from Lichen Symbiont
" I7 E- G" p9 X0 M. XR. Bandichhor · B. Nosse · O. Reiser . . . . . . . . . . . . . . . . . . . . . . .. . 43
! S- ]1 [$ Z' a* B6 vRecent Progress in the Total Synthesis of Dolabellane7 P5 n% n8 m, a& K6 B8 j7 [4 l
and Dolastane Diterpenes7 u# J, ~" v5 \# X
M. Hiersemann · H. Helmboldt . . . . . . . . . . . . . . . . . . . . . . . . . . . 736 u7 n2 a7 ^" ~" E4 B# W
Strategies for Total and Diversity-Oriented Synthesis
# A; z) w3 [/ `" Cof Natural Product(-Like) Macrocycles
# H. F2 M' J. uL.A. Wessjohann · E. Ruijter . . . . . . . . . . . . . . . . . . . . . . . . .. . . 137
( Y) A9 k/ x3 w* ]: YEnantioselective Synthesis of C(8)-Hydroxylated Lignans:% c/ J8 w( y% P" h9 x
Early Approaches and Recent Advances M. Sefkow . . .. . . . 185$ a8 x: ^+ u d% r
Author Index Volumes 201–243 . . . . . . . . . . . . . . . . . . . . . . . . . 225
4 J. J& s. b, s! E5 f! U- ?& ^Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 237
' B b: K: [' v9 d7 C% s" p8 Y# S' u; y% K' H; H
1 }* F7 T9 \/ f
, ~ S& s4 q$ F/ {% MNatural Products Synthesis II
9 f1 I8 ?+ A8 k1 {Targets, Methods, Concecpts4 ^1 D. c) W% i+ Z5 w5 e3 ^
6 V, {7 M- d5 C
Volume Editor: Johann Mulzer
& ^# z; A- x0 z7 r
0 l$ T" z4 `! x2 V3 ?. N4 E( OWith contributions by
" Q6 C. J; Z- cU. Beifuss · T. J.Heckrodt · M.Kalesse · H.-J.Knölker · P.Metz ·
1 c+ S( y' e( \& b% {J.Mulzer · U.Nubbemeyer · M. Tietze
) Q! a( U, T# \( g# X! ]
" @& O: t- x& O: q. @
% \6 f' G; M* Y4 ?" JContents
: J, ?) }3 i1 b3 }8 c7 A2 P, RMarine Natural Products from Pseudopterogorgia Elisabethae:
% s6 E" k. X+ F WStructures, Biosynthesis, Pharmacology and Total Synthesis6 j$ y& L# n# P$ G/ V5 l/ N
T. J.Heckrodt · J.Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
/ K6 t; j! X) H; |8 G* d' FRecent Advances in Vinylogous Aldol Reactions and their Applications m, v j5 s& }( z+ j' |
in the Syntheses of Natural Products0 T3 I/ g$ P4 L j4 Q4 {
M.Kalesse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43! x9 ]) B% [0 Q; V% o: [
Methanophenazine and Other Natural Biologically Active Phenazines5 w& K, F( X1 c/ H5 @% O3 v+ |5 L' r6 a
U. Beifuss · M. Tietze . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
5 P6 H" u# v" ^# V# O+ qOccurrence, Biological Activity, and Convergent Organometallic4 q. f, w5 y; `1 z! @
Synthesis of Carbazole Alkaloids. x. v+ P% A2 C7 c* I) B. ?% @' _
H.-J.Knoelker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1158 H8 t& b7 q$ \
Recent Advances in Charge-Accelerated Aza-Claisen Rearrangements
- o- ^2 A- V- OU.Nubbemeyer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149$ o& B8 I/ x, J) k9 p' f; `
Synthetic Studies on the Pamamycin Macrodiolides' p6 `3 p" A1 l: a2 ]) D
P.Metz . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 215
" b* T1 }! `; m- Q6 xAuthor Index Volumes 201–244 . . . . . . . . . . . . . . . . . . . . . . . . 2510 o, J, B) _; D1 q$ M+ M
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
/ u' J( K& |& {1部分共3个压缩卷，解压4.65M，含7个PDF文档
# I( e& l( c7 b# W& }! C4 J8 D2部分共3个压缩卷，解压5.23M，含8个PDF文档
. H" ~- P0 f* B, E. J
- W0 V b1 H8 p) W: X4 v[ 本帖最后由 fenglianxiang 于 2008-8-5 18:55 编辑 ] |
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发表于 2008-8-5 18:53:04
