|
|
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
《Comprehensive Asymmetric Catalysis I–III》，Springer出品，共12个压缩卷，解压后28.3M，共1479页。全书开头有以单词开头字母的索引。由众多专家共同编辑，是一个不对称催化反应不可多得的好书，里边有专家的简介和联系方式。压缩卷见2-4楼。6 O* r7 l4 V) J) L3 Q* V5 B# w
6 d; P) x2 C7 _0 F5 \Volume I
2 p) s( _6 ?! L. `1 Introduction
# d, M% R) i6 h6 hAndreas Pfaltz. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
/ J. O* u+ k8 ^2 Historical Perspective1 S! T2 X" U, i$ t. }: O. l6 k
Henri B. Kagan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 99 l- `# I+ [% X' M2 K
3 Basic Principles of Asymmetric Synthesis
8 D" h' @ b8 [- e& e* L, fJohann Mulzer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
5 D& F- }# [5 q P; S- c4 General Aspects of Asymmetric Catalysis
% Z7 x- x- k: @+ `4.1 Non-Linear Effects and Autocatalysis
# ?8 u; d2 ], J; u* i) QHenri B. Kagan, T. O. Luukas. . . . . . . . . . . . . . . . . . . . . . . . 1011 g0 c" [6 r: o v4 y. ~2 l
5Hydrogenation of Carbon-Carbon Double Bonds
( G+ E$ S- g: ?5.1 Hydrogenation of Functionalized Carbon-Carbon Double Bonds$ M- A& z3 B- w9 f. l7 |# j
John M. Brown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
$ w- z8 r" S$ V$ T% T5.2 Hydrogenation of Non-Functionalized Carbon-Carbon Double Bonds
: U0 H5 R. J: ^ Y( {Ronald L. Halterman . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1831 J+ Z6 E" t; f9 W% L" p' j
6 Reduction of Carbonyl and Imino Groups
, U2 M; T2 E# R8 X7 C/ M' g6.1 Hydrogenation of Carbonyl Groups S, [. D2 r' S$ e j
T. Ohkuma · R. Noyori . . . . . . . . . . . . . . . . . . . . . . . . . . . 199
) b$ i! _) k5 b) H, ~6.2 Hydrogenation of Imino Groups
, ^( H. A* G) v- e) U4 KHans-Ulrich Blaser, Felix Spindler . . . . . . . . . . . . . . . . . . . . 247
/ R: V, _7 l7 a3 V6.3 Hydrosilylation of Carbonyl and Imino Groups
' n" p+ n" `0 `* @, PHisao Nishiyama . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
& f8 @, }; N3 V* ^# W3 o% X" C6.4 Hydroboration of Carbonyl Groups8 b2 Q3 i }3 A
Shinichi Itsuno . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 289
' M, N$ C" d/ Y4 ~2 J- ]7 Hydrosilylation of Carbon-Carbon Double Bonds# _: p! J& r8 L F
Tamio Hayashi . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 319
8 {2 O4 @+ `1 F- b! s5 D; s8 Hydroalumination of Carbon-Carbon Double Bonds6 F6 |4 J* S. S5 t/ i" V3 s
Mark Lautens, Tomislav Rovis. . . . . . . . . . . . . . . . . . . . . . . 337, N8 ]1 k7 D8 n" k7 D2 f1 a
9 Hydroboration of Carbon-Carbon Double Bonds
! m% J+ \9 D0 y1 ATamio Hayashi . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3514 k, q9 v0 `' P a
10 Hydrocyanation of Carbon-Carbon Double Bonds8 d: K. |- F! L6 |
T.V. RajanBabu, Albert L. Casalnuovo. . . . . . . . . . . . . . . . . . . 367& J" z {1 y/ o: z
11 Hydrocarbonylation of Carbon-Carbon Double Bonds
`* I( D2 i( J3 a4 k' {( w$ mKyoko Nozaki . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3816 P5 g$ h4 K5 x! ?; h5 ~9 b
12 Hydrovinylation of Carbon-Carbon Double Bonds d* s. V( F) ?# s
T.V. RajanBabu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 417
0 f3 O% b$ q3 r! ?13 Carbometalation of Carbon-Carbon Double Bonds
! ~+ o- N9 r( Q2 \6 q) r; o2 YAmir H. Hoveyda, Nicola M. Heron . . . . . . . . . . . . . . . . . . . . 4314 M1 H, o$ U/ N! P0 n8 F# x$ m, m5 x
14 Heck Reaction% W8 x* A% T/ N- ~
Masakatsu Shibasaki, Erasmus M. Vogl. . . . . . . . . . . . . . . . . . 457: g1 R Q7 x8 ]# b
Volume II( J8 G0 x9 m: B
15 Pauson-Khand Type Reactions; k! j& }+ h) p( Y9 y) ^
Stephen L. Buchwald, Frederick A. Hicks. . . . . . . . . . . . . . . . . 491
( j% y2 S" n( k* p$ u16 Cyclopropanation and C-H Insertion Reactions
# T4 [; `; t0 F' I8 V16.1 Cyclopropanation and C-H Insertion with Cu
7 B m0 U6 i4 k* L( tAndreas Pfaltz. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5139 `; u# P$ V/ s
16.2 Cyclopropanation and C-H Insertion with Rh
0 V! J0 V# S* Z3 E' fKevin M. Lydon, M. Anthony McKervey . . . . . . . . . . . . . . . . . 539& T, v$ W# `; W' ?! C. B
16.3 Cyclopropanation and C-H Insertion with Metals
. ~/ f" p( z; g2 AOther Than Cu and Rh9 v6 p/ C, R9 j* q- _
André B. Charette, Hélène Lebel. . . . . . . . . . . . . . . . . . . . . . 581' ^. M, y' C8 G0 d1 X- L
17 Aziridination0 V1 _ d6 J5 @) Q; `! W
Eric N. Jacobsen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6075 h9 t v7 E$ \8 I
18 Epoxidation6 ?- D3 `# p! b( `$ o' w, |) Q1 e
18.1 Epoxidation of Allylic Alcohols' j+ a, n$ B5 ^; |6 P$ R) ?
Tsutomu Katsuki . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 621
/ g/ g1 z" t; H9 V% j2 i18.2 Epoxidation of Alkenes Other than Allylic Alcohols
* K0 J! r0 U1 Q2 ~, Z$ A0 FEric N. Jacobsen, Michael H. Wu. . . . . . . . . . . . . . . . . . . . . . 649
4 q' c# ~# `1 N: X' B( h18.3 Epoxide Formation of Enones and Aldehydes ; Q* t$ {; {/ X7 T7 m: r- ]6 i# c
Varinder K. Aggarwal. . . . . . . . . . . . . . . . . . . . . . . . . . . . 679# s2 v) ~/ T' G( \+ s# [5 d
19 Oxidation of Sulfides- l9 |9 T. R( a3 w* r8 n) i' n: t
Carsten Bolm, Kilian Muniz, Jens P. Hildebrand. . . . . . . . . . . . . 697
, l8 A; f) g P20 Dihydroxylation of Carbon-Carbon Double Bonds
+ d( M7 ?4 M; G& e. p- NIstvan E. Markó, John S. Svendsen. . . . . . . . . . . . . . . . . . . . . 7139 l H b+ M$ m$ U; l+ N
21 C-H Oxidation
+ a( B3 W9 M7 v, w1 \Tsutomu Katsuki . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 791
+ _; J3 O% I+ Y4 k* t22 Baeyer-Villiger Reaction) [* a- y' D6 ?' e
Carsten Bolm, Oliver Beckmann . . . . . . . . . . . . . . . . . . . . . 8037 {0 c1 @) t4 A2 S% p( W! e7 O9 |
23 Isomerization of Carbon-Carbon Double Bonds
% a* u3 n) p4 g! R$ Y$ ASusumu Akutagawa. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 813
5 t; O0 V5 G; v; h3 _24 Allylic Substitution Reactions
$ y; X' ]* j( BAndreas Pfaltz, Mark Lautens . . . . . . . . . . . . . . . . . . . . . . . 833- C* U; E" P' B. L6 P6 c
25Cross-Coupling Reactions
9 C- _2 m/ D, mTamio Hayashi . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 887: B8 K) I5 Z8 O9 e% t4 O- Q7 |
26 Alkylation of Carbonyl and Imino Groups; [/ I3 j1 |( m/ e0 F9 l2 V& k
26.1 Alkylation of Carbonyl Groups
$ F' Y; x9 q% o9 m5 P" ?Kenso Soai, Takanori Shibata . . . . . . . . . . . . . . . . . . . . . . . 911
4 O; Q8 M8 A$ V; ?26.2 Alkylation of Imino Groups
" p$ i Q8 n4 P/ s9 \' MScott E. Denmark, Olivier J.-C. Nicaise. . . . . . . . . . . . . . . . . . 923
/ Y6 }9 P Y# Q! { U6 L27 Allylation of Carbonyl Groups
" j! @. q: l3 Q* rAkira Yanagisawa . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9657 y3 d" d8 @, [( \' _+ Z
28 Cyanation of Carbonyl and Imino Groups4 y; p/ N* ]- X0 ^, E
Atsunori Mori, Shohei Inoue . . . . . . . . . . . . . . . . . . . . . . . 983 D2 d7 x5 C/ a4 y) ]7 }" n
Volume III1 R3 n4 c' T* i5 m0 t4 u J( i% M
29 Aldol Reactions3 n3 `3 K3 U. t0 }% V
29.1 Mukaiyama Aldol Reaction
P k' T( ^$ D) f5 R+ t2 AErick M. Carreira . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 997
% ?# O! N" x/ `$ n+ @9 i0 T29.2 Addition of Isocyanocarboxylates to Aldehydes# [5 j3 A4 d" {5 e
Ryoichi Kuwano, Yoshihiko Ito . . . . . . . . . . . . . . . . . . . . . . 10670 I L$ @8 Y$ u: |
29.3 Nitroaldol Reaction1 H, v' p5 i3 y: c9 H
Masakatsu Shibasaki, Harald Groger. . . . . . . . . . . . . . . . . . . 1075
! d4 S: s K, I4 p8 R! O% k30 Addition of Acyl Carbanion Equivalents to , ], B: X. L9 S! E5 H( u+ g, o
Carbonyl Groups and Enones
) ~0 @/ a9 @- W( l( JDieter Enders, Klaus Breuer. . . . . . . . . . . . . . . . . . . . . . . . 1093" N+ L+ r7 v, I9 @) V b" W
31 Conjugate Addition Reactions5 ]$ M/ X$ N' _3 y/ C6 _4 ^$ I
31.1 Conjugate Addition of Organometallic Reagents
" X) a2 I# x; `7 y @Kiyoshi Tomioka, Yasuo Nagaoka. . . . . . . . . . . . . . . . . . . . . 1105 K& [$ W! f3 R
31.2 Conjugate Addition of Stabilized Carbanions
6 j4 V) ?; c& S. X4 {5 U2 \+ iMasahiko Yamaguchi. . . . . . . . . . . . . . . . . . . . . . . . . . . . 11216 q) E0 a: g k7 ]
32 Ene-Type Reactions
: ?# t) M. K' r3 tKoichi Mikami, Masahiro Terada . . . . . . . . . . . . . . . . . . . . . 11439 t6 k! l& A6 Q) }5 ^5 V
33 Cycloaddition Reactions
; ~. x# [, J9 i33.1 Diels-Alder Reactions, p' w5 z& a9 i H: k
David A. Evans, Jeffrey S. Johnson . . . . . . . . . . . . . . . . . . . . 1177
& G+ M& h( ~1 G, h2 N0 V33.2 Hetero-Diels-Alder and Related Reactions0 D2 q. S) u; A$ [
Takashi Ooi, Keiji Maruoka . . . . . . . . . . . . . . . . . . . . . . . . 1237
9 f, @2 X# m/ T$ k$ q' n33.3 [2+2] Cycloaddition Reactions
& N9 t# [6 m! D, A4 V! m# {Yujiro Hayashi, Koichi Narasaka . . . . . . . . . . . . . . . . . . . . . 1255
# g/ n, S8 N( {1 d34 Additions to Enolates
9 @* V1 t7 Y4 r: k# Z: ~34.1 Alkylation of Enolates
& p4 t( O2 w. U# a& c- jDavid L. Hughes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1273
! l" q. D% b% r9 O4 @34.2 Protonation of Enolates' u& A% u5 c% v( {
Akira Yanagisawa, Hisashi Yamamoto . . . . . . . . . . . . . . . . . . 1295% ], p( V. q$ r2 I; d
35Ring Opening of Epoxides and Related Reactions) G4 C$ \- E% e% b2 X' j
Eric N. Jacobsen, Michael H. Wu. . . . . . . . . . . . . . . . . . . . . . 1309
0 ^: Q" T5 H, k* L) y36 Polymerization Reactions* p+ [5 u! { ~' a! v6 a1 K2 J9 J- p
Geoffrey W. Coates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1329" `+ @) M# z3 d
37 Heterogeneous Catalysis
; Z& ~0 A* S2 }* ]7 R1 uHans-Ulrich Blaser, Martin Studer . . . . . . . . . . . . . . . . . . . . 1353
' X2 k% M% \) w' u6 M; F; t38 Catalyst Immobilization) i6 x8 Q. e( u+ z) W3 j
38.1 Catalyst Immobilization: Solid Supports
- d+ M! H8 r2 i7 IBeno^?t Pugin, Hans-Ulrich Blaser. . . . . . . . . . . . . . . . . . . . . 13678 Q4 I/ j' X h) ]0 o; O
38.2 Catalyst Immobilization: Two-Phase Systems! |: |3 M% T* ]* a! r a
Günther Oehme . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1377% J; J' o' C- W* g6 h, w" P: B' _( r
39 Combinatorial Approaches" M6 T& H( a8 L7 G0 l |' b! n3 g
Ken D. Shimizu, Marc L. Snapper, Amir H. Hoveyda . . . . . . . . . . 1389% K7 G8 {& Z& G
40 Catalytic Antibodies7 R4 d3 z W. A6 H, S7 b9 W
Paul Wentworth Jr., Kim D. Janda . . . . . . . . . . . . . . . . . . . . . 1403
, j! \- h' e1 C1 F8 X41 Industrial Applications3 y7 t, d/ `/ R2 x& B3 M/ k
41.1 The Chiral Switch of Metolachlor
0 P. F' r3 H2 R; V0 b' XHans-Ulrich Blaser, Felix Spindler . . . . . . . . . . . . . . . . . . . . 1427
. ^: d; N1 T/ B+ q* Q) s, {41.2 Process R&D of Pharmaceuticals, Vitamins,
5 J* y4 i* u5 I- s+ _7 sand Fine Chemicals. M' Z1 R1 `9 V9 P: n ^/ {
Rudolf Schmid, Michelangelo Scalone . . . . . . . . . . . . . . . . . . 1439
* B0 z1 ]5 U1 b2 T7 C( ?$ K41.3 Cyclopropanation
1 b. b4 J: c/ y# y& LTadatoshi Aratani . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1451; b; [9 F9 p! q+ v" R
41.4 Asymmetric Isomerization of Olefins8 X5 r* ~) Q/ T
Susumu Akutagawa. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1461" x. i( W. Z* v: s. w9 F2 e
42 Future Perspectives in Asymmetric Catalysis
6 k* H; n8 q: XEric N. Jacobsen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1473; b* u4 @( u. m0 k* k; m" ]% g0 w
Subject Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1479 |
|
[复制链接]
发表于 2008-6-22 17:09:42
楼主