Добавил:
ivanov666
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Хиральные лиганды в асимметрическом катализе. Монография
.pdf
itaconic acid derivatives catalyzed by a modified DIOP
-rhodium
complex / T. Mori
Lett.
rhodium and a chiral bisphosphine / W.S.Knowles, M.J.Sabacky,
B.D.Vineyard, D.J.Weinkauff // J. Am. Chem. Soc.
Vol.97.
bisphosphine catalyst / B.D. Vineyard, W.S. Knowles, M.J.
Sabacky, G.L. Bachman, D.J. Weinkauff // J. Am. Chem. Soc.
1977.
Acc. Chem. Res.
binaphthyl (BINAP), an atropisomeric chiral
bis(triaryl)phosphine, and its use in the
asymmetric hydrogenation of .alpha.
Miyashita, A. Yasuda, H. Toriumi, T. Ito, T. Souchi, R. Noyori
// J. Am. Chem. Soc.
bis(diarylphosphino)
K.Mashima, K.Koyano, M. Yagi, H. Kumobayashi, T.Taketomi,
S. Akutagawa, R. Noyori // J. Org. Chem.
No.5.
// In “Applied Homogeneous Catalysis with Organometallic
Compounds”. Applications. Vol. 1 Ed. by B. Cornils, W. A.
Herrmann. VCH, Weinheim
Tokyo.
highly enantioselective hydrogenation reactions / M.J. Burk // J.
Am. Chem. Soc.
Preparation of Novel Amino Acids and Peptides / M.J. Burk,
J.R. Lee, J.P.Martinez // J. Am. Chem. Soc.
moto, M. Chiba, K. Achiwa // Tetrahedron
–1989.- Vol.30.- P.735-738.
30. Knowles, W.S. Asymmetric hydrogenation with a complex of
–1975.-
- No. 9.- P.2567-2568.
31. Vineyard, B.D. Asymmetric hydrogenation. Rhodium chiral
–
- Vol.99.- No.18.- P.5946-5952.
32. Knowles, W.S. Asymmetric hydrogenation / W.S. Knowles //
–1983.- Vol.16.- No.3.- P.106-112.
33. Miyashita, A. Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-
rhodium(I)-catalyzed
-(acylamino)acrylic acids/A.
- 1980.- Vol.102.- No.27.- P.7932-7934.
34. Takaya, H. Practical synthesis of (R)- or (S)-2,2'-
-1,1'-binaphthyls (BINAPs) / H.Takaya,
–1986.- Vol.51.-
- P.629-635.
35. Noyori, R. Asymmetric synthesis / R. Noyori, S. Hashiguchi
-New York-Basel-Cambridg-
-1996. - P. 552.
36. Burk, M.J. C2-symmetric bis(phospholanes) and their use in
–1991.- Vol.113.- No.22.- P. 8518-8519.
37. Burk, M.J. A Versatile Tandem Catalysis Procedure for the
–1994.- Vol. 116.-
221
No. 23.
- P.10847-10848.
tric catalysis / M. J. Burk, J. E. Feaster, R. L. Harlow // Organ
metallics.
Transition Metal Compounds. Vol. II / H. Brunner, W. Zettlme
er //
cent trends and new developments / H.
Pugin, F. Spindler, H. Steiner, M. Studer // Adv. Synth. Catal.
2003.
dation / T. Katsuki, K.B. Sharpless // J. Am. Chem. Soc.
1980.
hydrogenation. Rhodium(I) complexes of dehydroamino acids
containing asymmetric ligands r
diphenylphosphino)ethane
Chem. Soc.
the asymmetric catalytic hydrogenation of a prochiral olefin
S. C. Chan, J. J
Vol. 102.
талитических реакциях гидрирования, гидросилилирования,
кросс
Ус
конфигурационные отношения в асимметрических катал
тических реакциях под действием металлокомплексов / В.А.
Павлов // Успехи химии.
1307.
lyzed by rhodium complexes with chiral pyrrolidinodipho
phines. Crucial factors for the effective asymmetric
38. Burk, M.J. New electron-rich chiral phosphines for asymme-
o-
- 1990.- Vol. 9.- No10.- P. 2653-2655.
39. Brunner, H. Handbook of enantioselective Catalysis with
i-
Ligands-References WCH.- Weinheim.- 1993.- P. 359.
40. Blaser, H.-U. Selective hydrogenation for fine chemicals: Re-
-U. Blaser, C. Malan, B.
–
- Vol.345.- No 1+2. - P.103-151.
41. Katsuki, T. The first practical method for asymmetric epoxi–
-Vol.102.- P.5974.
42. Brown, J. M. The mechanism of asymmetric homogeneous
elated to bis(1,2-
/ J.M. Brown, P.A. Chaloner // J. Am.
– 1980 – Vol. 102 – No 9. – P.3040–3048.
43. Chan, A. S. C. Identification of the enantioselective step in
/ A.
. Pluth, J. Halpern // J. Am. Chem. Soc. - 1980 –
- No18. – P. 5952–5954.
44. Павлов, В.А. Механизм асимметрической индукции в ка-
-сочетания на комплексах металлов / В.А. Павлов //
пехи химии. – 2002. – Т. 21. - №1. – С. 39-56.
45. Павлов, В.А. Центральная хиральность атома металла и
– 2004. – Т. 73. - №12. – С. 1269-
46. Ojima, I. Asymmetric hydrogenation of prochiral olefins cata-
222
и-
s-
induction / I.
Ojima, T. Kogure, N. Yoda // J.Org. Chem.
– 1980. – Vol.45. –
No 23.
lyzed by a Rhodium Complex of (S,S)
butylmethylphosphino)ethane. Dihydride Mechanism of Asy
metric Hydrogenation
T. Imamoto // J. Am. Chem. Soc.
P.7183
Rh
Mechanism
to // J. Am. Chem. Soc.
5276.
ского гидрирования с хиральным лигандом
Павлов, А.А. Волобоев, Л.С.Горшкова, Е.И. Клабуновский //
Докл.
вие бисдифенилфосфиновых комплексов родия. Сообщение
2. (2
дифенилфосфинамино
(1,5
парирования. / В.А. Павлов, А.А. Волобоев, Л.С.Горшкова,
Е.И. Карпейская, Е.И. Клабуновский // Изв.
Хим.
// Wiley.
B. Jandeleit, D.J. Schaefer, T. S. Powers, H. W. Turner, W. H.
Weinberg // Angew. Chem. Int. Ed.
2532.
// Science (Washington, DC, US).
P. 1691
– PP.4728-4739.
47. Gridnev I.D. Mechanism of Asymmetric Hydrogenation Cata-
-1,2-Bis(tertm-
/ I. D. Gridnev, N. Higashi, K. Asakura,
– 2000 – Vol. 122 – No 30. –
–7194.
48. Gridnev I.D. Asymmetric Hydrogenation of Enamides with
-BisP* and Rh-MiniPHOS Catalysts. Scope, Limitations, and
/ I. D. Gridnev, M. Yasutake, N. Higashi, T. Imamo-
– 2001. – Vol. 123. - No22. – P.5268–
49. Павлов, В.А. Новый родиевый катализатор асимметричеPheNOP. / В.А.
АН СССР.- 1985 – Т.283. – С. 1206-1208.
50. Павлов, В.А. Асимметрическое гидрирование в присутст-
R)—3— фенил—2N—метил—2N—
— 1 —дифенилфосфорокси пропан-
-циклооктадиен) родий (1)-перхлорат — катализатор
АН СССР. Сер.
– 1987.- № 3.- С. 513-518.
51. Combinatorial Chemistry. Eds.: S.R. Wilson, A.W. Czarnik.
- New York.- 1997.
52. Jandeleit, B. Combinatorial materials science and catalysis /
– 1999.- Vol. 38.- P. 2494-
53. Yoon, T. Privileged chiral catalysts / T. Yoon, E.N. Jacobsen
– 2003.- Vol. 299.- No5613.-
-1693.
54. Breit, B. Supramolecular approaches to generate libraries of
223
chelating bidentate ligands for homogeneous catalysis / B. Breit
// Angew. Chem. Int. Ed.
– 2005.- Vol. 44. - No42. - P. 6816-
6825.
nation Reactions Based on Chiral Monophosphite Ligands /
M.T.
No.21
tion using chiral monophosphonite ligands / M.T. Reetz, T. Cell
// Tetrahedron Lett.
for asymmetric hydrogenation: factors controlling the reactivities
and enantioselectivities / D. Liu, W. Li, X. Zhang // Tetrah
dron: Asymmetry.
tric catalysis / H.B. Kagan, J.C. Fiaud, C. Hoornaert, D. Meyer
J.C. Poulin // Bulletin des Societes Chimiques Belges.
Vol. 88.
(diphenylphosphino) hexane and its application in Rh
highly enantioselective hydrogenation of enamides / W. Li, X.
Zhang // J. Org. Chem.
Phosphoramidite Ligands Derived from Quinoline (QUIN
PHOS) / G. Francio, F. Faraone, W. Leither // Angew. Chem.
Int. Ed.
phosphine for Highly
Alkylation, and Hydroboration Reactions / A. Togni, C. Breutel,
A. Schnyder, F. Spindler, H. Iandert, A. Tijani // J.Am.Chem.
Soc.
2,2
thesis of atropisomeric diphosphine ligands / M. Ceregetti, W.
Arnold, E. Broger, A. Rageot // Tetrahedron Lett.
55. Reetz, M.T. Highly Enantioselective Rh-Catalyzed Hydroge-
Reetz, G. Mehler//Angew. Chem. Int. Ed.- 2000.- Vol.39.-
- P.3889-3890.
56. Reetz, M.T. Rhodium-catalyzed enantioselective hydrogena-
–2000.- Vol.41.- P.6333-6336.
57. Liu, D. Development of DIOP derivatives as efficient ligands
e-
- 2004.- Vol.15.- No14.- P. 2181-2184.
58. Kagan, H. B. Synthesis of new chiral phosphines for asymme-
- 1979.-
- No11.- P. 923-931.
59. Li, W. 4-O-isopropylidene-(3S,4S)-dihydroxy-(2R,5R)-bis
-catalyzed
- 2000.- Vol. 65.- No18.- P. 5871-5874.
60. Francio, G. Asymmetric Catalysis with Chiral Phosphane /
A-
–2000.- Vol. 39.- No.8.- P.1428-1430.
61. Togni, A. A Novel Easily Accessible Chiral Ferrocenyldi-
Enantioselective Hydrogenation, Allylic
–1994.- Vol.116.- No.9.- P.4062-4066.
62. Ceregetti, M. (R)- and (S)-6,6′-dimethyl- and 6,6′-dimethoxy-
′-diiodo-1,1′-biphenyls: Versatile intermediates for the syn-
224
-1996.-
Vol.37.
- No.30.- P. 5347-5350
металлов. В 2
Нортон, Р. Финке // “Мир”.
a Narrow Dihedral Angle in the Biaryl Backbone
Yokozawa, T. Ishizaki, T. Moroi, N. Sayo, T. Miura, H. Kum
bayashi // Adv. Synth. Catal.
267.
tates Catalyzed by Ru
W. Tang, M. Lin, X. Zhang // Org. Lett.
25.
gands / H. Shimizu, I. Nagasaki, T. Saito // Tetrahedron
Vol.61.
Bite Angles and Their Applications in Asymmetric Hydrogen
tion of
J. Org. Chem.
enol acetates catalyzed by a Rh
Xiao, Z. Zhang, P. Cao, X. Zhang // Angew. Chem. Int. Ed.
1999.
of
Pure Amino Alcohols / A. Lei, S. Wu, M. He, X. Zhang // J. Am.
Chem. Soc.
Olefins of Cyclic
Zhang // J. Am. Chem. Soc.
9571.
Dihedral Angle Based on a Chiral Spirobifluorene Backbone / X.
Cheng, Q. Zhang, J.
63. Коллмен, Дж. Металлоорганическая химия переходных
-х частях. / Дж. Коллмен, Л. Хигедас, Дж.
- Москва.- 1989.- ч.1.- 502 стр.
64. Saito, T. New Chiral Diphosphine Ligands Designed to have
/ T. Saito, T.
o-
–2001.- Vol.343.- No.3.- P.264-
65. Wu, S. Highly Enantioselective Hydrogenation of Enol Ace-
-TunaPhos Complexes / S. Wu, W. Wang,
–2002.- Vol. 4.- No.
- P.4495-4497.
66. Shimizu, H. Recent advances in biaryl-type bisphosphine li– 2005.-
- P.5405-5432.
67. Zhang, Z. Synthesis of Chiral Bisphosphines with Tunable
a-
-Ketoesters / Z. Zhang, H. Qian, J. Longmire, X. Zhang //
-2000.- Vol.65.- No.19.- P.6223-6226
68. Jiang, Q. Highly enantioselective hydrogenation of cyclic
-PennPhos complex / Q. Jiang, D.
- Vol.38.- No4. – P.516-518.
69. Lei, A. Highly Enantioselective Asymmetric Hydrogenation
-Phthalimide Ketone: An Efficient Entry to Enantiomerically
-
–2004.- Vol.126.- No.6. P.1626-1627.
70. Tang, W. Enantioselective Hydrogenation of Tetrasubstituted
-(Acylamino)acrylates / W. Tang, S. Wu, X.
–2003.- Vol.125.- No. 32.- P. 9570-
71. Cheng X. Highly Rigid Diphosphane Ligands with a Large
-H. Xie, L.-X. Wang, Q.-L. Zhou // Angew.
225
Chem.
–2005.- Vol. 117.- P. 1142-1145.
pholanes and their applicatio
tions / T. Riermeier, A. Monsees, J. Holz, A. Borner // Chem
stry Today.
gands in Asymmetric Catalysis: Electronic Effects and Depe
dence of Backbo
drogenations. Synthesis of R
Sugars as Ligand Precursors / T.V. RajanBaby, T.A. Ayers, G.A.
Halliday, K.K. You, J.C. Calabrese // J. Org. Chem. 1997.
Vol.62.
tion / O. Pamies, M. Dieguez, A. Ruiz, C. Claver // Chimica oggi
Chemistry Today 2004.
ing a soluble optically
M. J. Sabacky // Chem. Comm.
ically Active Phosphinerhodium Complex in Homogeneous
Solution / L. Horner, H. Siegel, H. But
Ed.
lyzed hydrogenations of terpenic and .alpha.
substituted
Priester, R. C. Sun, K. Toth, G. J. Saucy // Org. Chem.
No 45.
nylphosphine. Epimeric, chiral, tertiary phosphine ligands for
asymmetric synthesis
Chem.
their use as ligands in rhodium(I) complexes
Mathey, L. Ricard // Organometallics
1212.
72. Riermeier, T. CatASium-M – a new family of chiral bisphosn in enantioselective hydrogena-
i-
–2004.- P.22-24
73. RajanBaby, T.V. Carbohydrate Phosphinites as Practical Li-
n-
ne Chirality in Rh-Catalyzed Asymmetric Hy-
- or S-Amino Acids Using Natural
- No.17.- P.6012-6028.
74. Pamies, O. Sugar-based P-ligands for asymmetric hydrogena-
- No 10. –P.12-17.
75. Knowles, W. S. Catalytic asymmetric hydrogenation employ-
active rhodium complex / W. S. Knowles,
– 1968.- Vol.22.- P. 1445-1446.
76. Horner, L. Asymmetric Catalytic Hydrogenation with an Opt-
he // Angew. Chem. Int.
–1968.- Vol.7- No. 12- P.942-943.
77. Valentine, D. Rhodium chiral monophosphine complex cata-
-(acylamino)-
acrylic acids / D., Jr. Valentine, K. K. Johnson, W.
-1980. -
– P.3698–3703.
78. Morrison, J. D. Synthesis of methyl- and neomenthyldiphe-
-
/ J. D. Morrison, W. F. Masler // J. Org.
– 1974. - No39 – P.270–272.
79. Marinetti, A. Synthesis of optically active phosphiranes and
/ A. Marinetti, F.
- 1993. – No12 – P.1207–
226
80. Marinetti, A. Phosphetanes as Chiral Ligands for Catalytic
Asymmetric Reactions: Hydrosilylation of Olefins
ti, L. Ricard // Organometallics
P.3956
lytic applicati
Genêt // Chimie
tion, and
Burk, J.E. Feaster, R.L. Harlow // Tetrahedron: Asymmetry
1991
chiral monophosphine ligand: 2,5
F. Guillen, M. Rivard, M. Toffano, J.
C. Fiaud // Tetrahedron.
through the synthesis and resolution of the chiral trans
diphenylphospholanic acid
dron Lett.
Chiral Ligands and Their Application in Catalytic Asymmetric
Hydrogenations / M. Ostermeier, J. Prieß, G. Helmchen // A
gew. Chem., Int. Ed.
and their use in asymmetric hydrogenation
Oehme, A. Monsees, T. Riermeier, U. Dingerdissen, M
Tetrahedron Lett.
Homogeneous Catal.
Ferrocenecarboxaldehydes
Taudien, H. B. Kagan // J. Org. Chem.
P.6733
and Homogeneous Hydrogenation Reactions with Their Rh
/ A. Marinet-
– 1994 – Vol.13. - No10. -
– 3962.
81. Marinetti, A. Recent developments in the synthesis and cata-
ons of chiral phosphetanes / A. Marinetti, J.-P.
– 2003. – Vol.6 – No4. – P.507–514.
82. Burk, M. J. New chiral phospholanes; Synthesis, characteriza-
use in asymmetric hydrogenation reactions / M. J.
–
– Vol.2 – No7. – P.569–592.
83. Guillen, F. Synthesis and first applications of a new family of
-diphenylphosphospholanes /
-Y. Legros, J.-C. Daran, J.-
– 2002. – Vol.58. – P.5895–5904;
84. Guillen, F. Enantiomerically pure 1,2,5-triphenylphospholane
-(2,5)-
/ F. Guillen, J.-C. Fiaud // Tetrahe-
– 1999. – Vol.40. - P.2939–2942.
85. Ostermeier, M. Mono- and Bidentate Phosphinanes—New
n-
- 2002. – Vol.41 – P.612– 614.
86. Junge, K. Synthesis of new chiral monodentate phosphines
/ K. Junge, G.
. Beller //
– 2002. - No43 – P.4977–4980.
87. Gladiali, S.; Murruzzu, C.; Pilo, L.; Taras, R. 13th Int. Symp.
- Tarragona. – 2002. - P055. – P.105.
88. Riant, O. An Efficient Asymmetric Synthesis of 2-Substituted
/ O. Riant, O.Samuel, T. Flessner, S.
– 1997. – Vol. 62. –
–6745.
89. Saito, S. Syntheses of Novel Sugar Phosphine Derivatives,
o-
227
dium Com
plexes / S. Saito, Y. Nakamura, Y.Morita // Chem.
Pharm. Bull.
phosphonites and phosphines as ligands in Rh
genation of N
approach / M. T. Reetz, G. Mehler, A. Meiswinkel // Tetrah
dron: Asymmetry.
nation Reactions Based on Chiral Monophosphite Ligands / M.
T
–
trical Synthesis / M.T. Reetz, G. Mehler, A. Meiswinkel //
Patent application.
of Vinyl Carboxylates with Monodentate Phosphite Ligands
M.T. Reetz, L.J. Goossen, A. Meiswinkel, J. Paetzold, J.
F.Jensen // Org. Lett.
tion using chiral monophosphonite ligands
// Tetrahedron Lett.
phorus(III) ligands that outperform their chelating analogues in
asymmetric hydrogenation catalysis / C. Claver, E. Fernandez,
A. Gillon, K. Heslop, D. J. Hyett, A. Martorell, A. G. Orpen, P.
G. Pringle // Chem. Commun. (Cambridge, UK)
961
rhodium
J.
Vol.15.
nation Reactions Based on Chiral Monophosphite
T. Reetz, G. Mehler // Angew. Chem., Int. Ed.
–
– 1985. – Vol. 33. – P.5284–5293.
90. Reetz, M. T. Mixtures of chiral monodentate phosphites,
-catalyzed hydro-
-acyl enamines: extension of the combinatorial
e-
– 2004. – Vol.15. – P.2165–2167.
91. Reetz, M. T. Highly Enantioselective Rh-Catalyzed Hydroge-
. Reetz, G. Mehler // Angew. Chem., Int. Ed. – 2000. – Vol.39.
P.3889–3890.
92. Reetz, M. T. Chiral Monophosphites as Ligands for Asymme-
– 2001. - WO 01/94278 A1.
93. Reetz, M. T. Enantioselective Rh-Catalyzed Hydrogenation
/
– 2003.- Vol.5. – No17. – P.3099–3101.
94. Reetz, M. T. Rhodium-catalyzed enantioselective hydrogena-
/ M. T. Reetz, T. Sell
– 2000. – Vol.41. – P.6333–6336.
95. Claver, C. Biarylphosphonites: a class of monodentate phos-
–962.
96. Jerphagnon T. Chiral monodentate phosphorus ligands for
-catalyzed asymmetric hydrogenation / T. Jerphagnon,
-L. Renaud, C. Bruneau // Tetrahedron: Asymmetry. – 2004. –
– P.2101–2111.
97. Reetz, M. T. Highly Enantioselective Rh-Catalyzed Hydroge-
– 2000. – Vol.39
P.3889–3890.
228
- 2000. – P.
Ligands / M.
98. Gergely, I. Enantioselective hydrogenation catalyzed by high-
ly active rhodium c
meric moieties
Szöllősy, A. Monsees, T. Riermeier, J. Bakos // Tetrahedron:
Asymmetry
Hydrogenation of 2
Convenient Access of Enantiomerically Pure Isoprenoid Buil
ing Blocks / M. Ostermeier, B. Brunner, C. Korff, G. Helmchen
// Eur. J. Org. Chem.
easily available monodentate phosphite ligands
Xiao // Tetrahedron Lett.
drate:
nation
Org. Lett.
Derived from d
oselective Rh
H. Luo, C. Bai, X. Hu, H. Chen
C
H.
2003.
Catalyzed Hydrogenation with Monodentate Ligands
den Berg, A. J. Minnaard, E. P. Schudde, J. van Esch, A. H. M.
de Vries, J. G. de Vries, B. L. Feringa // J. Am. Chem. Soc.
2000.
through in Rhodium
Olefins / M. van
man, E.P. Schudde, A.Meetsma, B.
omplexes of chiral phosphites with atropiso-
/ I. Gergely, C. Hegedüs, H. Gulyás, Á.
– 2003. – Vol.14 – P.1087–1090.
99. Ostermeier, M. Highly Enantioselective Rhodium-Catalyzed
-(2-Methoxy-2-oxoethyl)acrylic Acid − A
d-
– 2003. - No17. - P.3453–3459.
100. Chen, W. Enantioselective hydrogenation with inexpensive,
/ W. Chen, J.
– 2001. – Vol.42 - P.2897–2899.
101. Huang, H. Chiral Monophosphites Derived from Carbohy-
Conformational Effect in Catalytic Asymmetric Hydroge-
/ H. Huang, Z. Zheng, H. Luo, C. Bai, X. Hu, H. Chen //
– 2003 – Vol.5 - No22. – P.4137–4139.
102. Huang, H. A Novel Class of P−O Monophosphite Ligands
-Mannitol: Broad Applications in Highly Enanti-
-Catalyzed Hydrogenations / H. Huang, Z. Zheng,
// J. Org. Chem. – 2004. – Vol.69 - No7. – P.2355 - 2361.
103. Dreisbach, C. Chiral monophosphorus compounds / F.Agel,
. Dr. Dreisbach, B. Dr. Driessen-Hölscher, B. Dr. Meseguer,
-C. Militzer, Th. Dr. Prinz, U. Dr. Scholz //Eur.Pat. Appl. –
- EP 1298136.
104. van den Berg, M. Highly Enantioselective Rhodium-
/ M. van
– Vol.122 – P.11539–11540.
105. van den Berg, M. Monodentate Phosphoramidites: A Break-
-Catalysed Asymmetric Hydrogenation of
den Berg, A.J.Minnaard, R.M. Haak, M. Lee-
L. Feringa, A.H. M. de
229
–
Vries, C.
E.P. Maljaars, C.E.Willans, D.Hyett, J.A. F. Boogers,
H.
Vol.345.
catalyzed by rhodium
X. Jia, R. Guo, X. Li, X. Yao, A.S.C Chan // Tetrahedron Lett.
2002.
dite Catalyst and Its Application in t
genation of Enamides and α
X.Jia, X.Li, L.Xu, Q.Shi, X. Yao, A.S.C. Chan // J. Org. Chem.
2003.
ficient and recyclable catalysts for asymmetric hydrogenation of
dimethylitaconate and dehydroamino acids and esters
ty, E. G. Robins, I. Pál, C.R. Newman, C. Hardacre, D.
D. A. Mooney // Tetrahedron: Asymmetry.
P.1517
catalyzed by rhodium
derived from H8
Yeung, K.
Asymmetry.
dium
G. Hu, H. Zhou, L.
(Cambridge, UK)
spirobiindane
tituent effect of SIPHOS ligands in Rh
hydrogenation / S.
Zhou // Tetrahedron: Asymmetry.
P.3219
cient Ligands for Rhodium
J. W. Henderickx, J. G. de Vries // Adv. Synth. Catal. 2003. –
– P.308–323.
106. Jia, X. Highly enantioselective hydrogenation of enamides
–monodentate phosphoramidite complex /
–
– Vol.43 – P.5541–5544.
107. Jia, X. Highly Efficient Rhodium/Monodentate Phosphorami-
he Enantioselective Hydro-
-Dehydroamino Acid Derivatives /
- Vol.68. – No 11. – P.4539–4541.
108. Doherty, S. Polymer-supported phosphoramidites: highly ef-
/ S. Doher-
Rooney,
– 2003. – Vol.14. –
–1527.
109. Li, X. Highly enantioselective hydrogenation of enamides
-monodentate phosphoramidite complex
-BINOL / X. Li, X. Jia, G.Lu, T. T.-L. Au-
-H. Lam, T.W.H. Lo, A.S.C. Chan // Tetrahedron:
– 2003. – Vol.14.- No18.- P. 2687–2691.
110. Fu, Y. Novel monodentate spiro phosphorus ligands for rho-
-catalyzed hydrogenation reactions / Y. Fu, J.-H. Xie, A.-
-X. Wang, Q.-L. Zhou // Chem. Commun.
– 2002. – P.480–481.
111. Zhu, S.-F. Synthesis of chiral 4,4′-disubstituted 1,1′-
-7,7′-diols and related phosphoramidites: the subs-
-catalyzed asymmetric
-F. Zhu, Y.Fu, J.-H.Xie, B. Liu, L. Xing, Q.-L.
- 2003.-Vol.14. – No20.-
–3224.
112.
Hu, A.-G. Monodentate Chiral Spiro Phosphoramidites: Effi-
-Catalyzed Enantioselective Hydro-
-
230
Соседние файлы в предмете [НЕСОРТИРОВАННОЕ]