Добавил:
ivanov666
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Хиральные лиганды в асимметрическом катализе. Монография
.pdf
Cobley, G. Casy // Adv. Synth. Catal.
–2003.- Vol.345.- No.1-
2.
gands: Synthesis, Structural Determination, and Applications in
the Ru
Pai, C.
Wong // J. Am. Chem. Soc.
11514.
ample of a new class of chi
phine ligands for transition metal catalyzed stereoselective rea
tions / T. Benincori, E. Brenna, F. Sannicolo, L. Trimarco, P.
Antognazza, E. Cesarotti // J.Chem. Soc. Chem. Comm.
Vol. 6.
Highly Efficient Transition Metal
Reactions: The Bis(diphenylphosphino) Five
roaryls / T. Benincori, E. Brenna, F. Sannicolo, L. Trimarco, P.
Antognazza, E.
–
bis(diphenylphoshino)
Easily Accessible, Chiral Biheteroaromatic Ligand for H
neous Stereoselective Catalysis / T. Benincori, E. Cesarotti, O.
Piccolo, F. Sannicolo // J. Org. Chem.
P. 2043
pensive, and efficient chiral diphosphine
ous stereoselective catalysis / T. Benincori, S. Gladiali, S. Rizzo,
F. Sannicolo // J. Org. Chem.
5942.
gands for stereoselective homogeneous catalysis by assembling
five
F. Sannicolo // J. Heterocyclic Chemistry.
- P.300-307.
193. Pai, C.-C. Highly Effective Chiral Dipyridylphosphine Li-
-Catalyzed Asymmetric Hydrogenation Reactions / C.-C.
-W. Lin, C.-C. Lin, C.-C. Chen, A.S.C. Chang, W. T.
- 2000.- Vol.122.- No.46.- P.11513-
194. Benincori, T. (Diphenylphosphino)-biheteroaryls: the first ex-
ral atropisomeric chelating diphos-
c-
– 1995.-
- P.685-686.
195. Benincori, T. New Class of Chiral Diphosphine Ligands for
-Catalyzed Stereoselective
-membered Bihete-
Cesarotti, F. Demartin, T. Pilati // J. Org. Chem.
1996.- Vol. 61.- No18.- P.6244-6251.
196. Benincori, T. 2,2',5,5'-Tetramethyl-4,4'-
-3,3'-bithiophene: A New, Very Efficient,
omoge-
– 2000.- Vol. 65.- No7.-
-2047.
197. Benincori, T. A new modular class of easily accessible, inex ligands for homogene-
– 2001.- Vol. 66.- No17.- P. 5940-
198 Benincori, T. Free design of chiral diphosphine chelating li-
-membered aromatic heterocycles / T. Benincori, S. Rizzo,
- 2002.- Vol. 39.-
241
No3.
- P.471-485.
a Narrow Dihedral Angle in the Biaryl Backbone / T. Saito, T.
Yokozawa, T. Ishizaki, T. Moroi, N.Sayo, T. Miura, H. Kum
bayashi // Adv. Synth. Catal.
267.
Bite Angles and Their Applications in Asymmetric Hydrogen
tion of
// J. Org. Chem.
ce
Pugin, F. Spindler, H. Steiner, M. Studer // Adv. Synth. Catal.
2003.
Imines Catalyzed by
Zhang // Angew Chem Int Ed Engl.
P.3425
gand. Highly stereoselective catalytic asymmetric hydrogenation
of prochiral carbon
Kumada//Tetrahedron Lett.
arylethanols by catalytic asymmetric hydrogenation / A. Kats
mura, M. Konishi, M. Kumada // Tetrahedron
20.
phine ligands / T. Hayashi // In Ferrocenes. Editor(s): A. Togni,
T. Hayashi. VCH.
phosphine for Highly Enantioselective Hydrogenation, Allylic
Alkylation, and Hydroboration Reactions / A. Togni, C. Breutel,
A. Schnyder, F. Spindler, H. Landert, A. Tijani // J. Am.Chem.
Soc.
199 Saito, T. New Chiral Diphosphine Ligands Designed to have
o-
–2001.- Vol.343.- No.3.- P.264-
200 Zhang, Z. Synthesis of Chiral Bisphosphines with Tunable
a-
-Ketoesters / Z. Zhang, H. Quian, J. Longmire, X.Zhang
–2000.- Vol.65.- No.19.- P.6223-6226.
201 Blaser, H.-U. Selective hydrogenation for fine chemicals: Re-
nt trends and new developments / H.-U. Blaser, C. Malan, B.
–
- Vol.345.- No1+2.-P.103-151.
202 Xiao, D. Highly Enantioselective Hydrogenation of Acyclic
Ir-f-Binaphane Complexes / D. Xiao, X.
–2001.- Vol. 40.- No.18.-
-3428.
203 Hayashi, T. A chiral (hydroxyalkylferrocenyl)phosphine li-
yl compounds / T. Hayashi, T. Mise, M.
–1976.- Vol.17.- P.4351-4354.
204 Katsumura, A. Asymmetric synthesis of 2-amino-1-
u-
Lett.- 1979.-Vol.
- P.425-428.
205 Hayashi, T. Asymmetric catalysis with chiral ferrocenylphos-
- Weinheim – 1995.- P.105-142.
206 Togni, A. A Novel Easily Accessible Chiral Ferrocenyldi-
–1994.- Vol. 116.- No.9.- P.4062-4066.
207
Hsiao, Y. Highly Efficient Synthesis of β -Amino Acid De-
242
rivatives via Asymmetric Hydrogenation of Unprotected En
a-
mines / Y. Hsiao, N. R. Rivera, T. Rosner, S. W. Krska, E. Njol
to, F. Wang, Y. Sun, J. D. Armstrong, E. J.J. Grabowski, R.D.
Tillyer, F. Spin
126.
termediates / H.
Switz.
No4.
technical applications / H.
Spindler, M. Studer, A. Togni // Solvias AG.
Topics in Catalysis.
sonal Account of an Industrial Odyssey in Asymmetric Catalysis
/ H.
P.17
opment of
U. Blaser, H.
Spindler, A.Wegmann // Chimia.
280.
and Practica
S.D. Debenham, E.B. Mackenzie, S.E. Large // Org. Lett.
2002.
Chiral Diphosphine Ligands Bearing Aromatic
(S,S)
1,1''
plexes / M. Sawamura, H. Hamashima, M. Sugawara,
R.Kuwano, Y. Ito // Organometallics.
P.4
diphosphine ligands. Application for catalytic asymmetric sy
i-
dler, C. Malan // J. Am. Chem. Soc. – 2004.- Vol.
- No32.- P.9918-9919.
208 Blaser, H.-U. Developing industrial processes for chiral in-
-U. Blaser, F. Spindler // Solvias AG. – Basel.-
- Chimica e l'Industria (Milan, Italy).- 2004.- Vol.86.-
- P.115-122.
209 Blaser, H.-U. Solvias Josiphos ligands: from discovery to
-U. Blaser, W. Brieden, B. Pugin, F.
- Basel.- Switz. -
- 2002.- Vol. 19.- No1. – P.3-16.
210 Blaser, H.-U. The Chiral Switch of (S)-Metolachlor: A Per-
-U. Blaser // Adv. Synth. Catal. –2002.- Vol.344.- No.1.-
-31.
211 Blaser, H.-U. The Chiral Switch of Metalachlor: The Devel-
a Large-Scale Enantioselective Catalytic Process / H.-
-P. Jalett, E. Jelsch, B. Pugin, H.-D. Schneider, F.
-1999.- Vol.53,- No.6-P.275-
212 Boaz, N.W. Phosphinoferrocenylaminophosphines as Novel
l Ligands for Asymmetric Catalysis / N.W. Boaz,
–
- Vol. 4.- No.14.- P.2421-2424.
213 Sawamura, M. Synthesis and Structures of Trans-Chelating
P-Substituents,
-(R,R)- and (R,R)-(S,S)-2,2''-Bis[1-(diarylphosphino)ethyl]-
-biferrocene (ArylTRAPs) and Their Transition Metal Com-
–1995.- Vol. 14.- No.10.-
549-4558.
214
Ito, Y. Design and synthesis of optically active trans-chelating
243
n-
thesis / Y. Ito, R. Kuwano // Phosphorus, Sulfur and Silicon and
the Related Elements.
- 1999.- Vol. 144-146.- P.469-472
Tetrahydropyrazine
Trans
Rhodium Complexes / R.
Kuwano, Y. Ito // Japan J. Org. Chem.
P.1232
ferrocenyl ligands for asymmetric catalysis / L. Schwink, P.
Knochel // Chemistry A.
No5.
amino FERRIPHOS as ligands for enantioselective Rh
preparation of chiral
Knochel // Tetrahedron: Asymmetry.
P.375
tuents in the
Asymmetric Hydrogenation of Functionalized Double Bonds / T.
Ireland, G. Grossheimann, C. Wieser
//Angew. Chem. Int. Ed.
Diphosphanylferrocene Ligands and Their Use in Enantiosele
tive Hydrogenation / T. Ireland, K. Tappe, G. Grossheimann, P.
Knochel // Chem.
plication in ruthenium
hydrogenations / K. Tappe, P. Knochel // Tetrahedron: Asymm
try.
Ligands for Asymmetric Catalysis / T. Sturm, L. Xiao, W. Wei
sensteiner // Chimia.
phosphine ligands for Rh
hydrogenation / W. Weissensteiner, T. Sturm, F. Spindler // Adv.
215 Kuwano, R. Asymmetric Hydrogenation of 1,4,5,6-
-2-(N-tert-butyl)carboxamide Catalyzed by
-Chelating Chiral Diphosphine-
- 1999.- Vol. 64.- No4.-
-1237.
216 Schwink, L. Enantioselective preparation of C2-symmetrical
- European Journal.- 1998.- Vol. 4.-
- P.950-968.
217 Perea, J. J. A. Synthesis and application of C2-symmetric di-
-catalyzed
α-amino acids / J.J.A. Perea, M. Lotz, P.
- 1999.- Vol. 10.- No2.-
-384.
218 Ireland, T. Ferrocenyl Ligands with Two Phosphanyl Substi-
positions for the Transition Metal Catalyzed
-Jeunesse, P. Knochel
–1999.- Vol. 38.- N. 21-P. 3212-3215.
219 Ireland, T. Synthesis of a New Class of Chiral 1,5-
c-
Eur. J. –2002.- Vol.8.- No.4.- P.843-852.
220 Tappe, K. New efficient synthesis of Taniaphos ligands: Ap-
- and rhodium-catalyzed enantioselective
- 2004.- Vol. 15.- No1.- P.91-102.
221 Sturm, T. Preparation of Novel Enantiopure Ferrocenyl-Based
–2001.- Vol.55.- No.9.- P.688-693.
222 Weissensteiner, W. A novel class of ferrocenyl-aryl-based di-
- and Ru-catalysed enantioselective
244
e-
s-
Synth. Cat.
– 2003.- Vol. 345.- No 1+2.- P. 160-164.
containing olefins catalyzed by BINAPHOS
T. Nanno
Asymmetry
Rh(I)
on the regioselectivity /
Organ.Chem.
for the rhodium
critical CO2 and fluorous solvents /
Hua
Chemistry
synthesis based on the demethylation of o
application in highly enantioselec
A. Suárez
Vol. 12.
Functionalities of Chiral Phosphine
Catalytic Enantioselective Hydrog
Méndez
–
platinum complexes of newchiral bisphosphites /
Szücs
Mono
BINOL Backbones and 1,3,2
Differences in the Enantioselectivity / K.N. Gavrilov, S.V. Zhe
lov, E. A. Rastorguev, N. N. Groshkin, M.G. Maksimova, E. B.
Benetsky, V.A. Davankov, M. T. Reetz // Adv. Synth. Catal.
201
223 Nanno, T. Asymmetric hydroformylations of sulfur-
—Rh(I) complexes /
, N. Sakai, K. Nozaki, H. Takaya / Tetrahedron:
. – 1995. – Vol. 6. – No 10. – P. 2583-2591.
224 Nozaki, K. Asymmetric hydroformylation catalyzed by an
-(R, S)-BINAPHOS complex: substituent effects in olefins
K. Nozaki, T. Nanno, H. Takaya // J.
– 1997. – Vol. 527. – No 1-2. – P. 103-108.
225 Bonafoux, D. Design and synthesis of new fluorinated ligands
-catalyzed hydroformylation of alkenes in superDominique Bonafoux, Zihao
, Beihan Wang, Iwao Ojima // Journal of Fluorine
. – 2001. – Vol. 112. – No 1. – P. 101-108.
226 Suárez, A. New chiral phosphine–phosphites: a convenient
-anisyl phosphines and
tive catalytic hydrogenations /
, A. Pizzano // Tetrahedron: Asymmetry. – 2001. –
– No 18. – P. 2501–2504.
227 Suárez, A. Electronic Differences between Coordinating
−Phosphites and Effects in
enation / A. Suárez, M. A.
-Rojas, A. Pizzano // Organometallics. – 2002. – Vol.21.
No 22. – P.4611–4621.
228 Cserépi-Szücs, S. Asymmetric hydroformylation catalysed by
S. Cserépi-
, J. Bakos // Chem. Commun. – 1997. – P. 635-636.
229 Gavrilov, K.N. Asymmetric Catalytic Reactions Using P*-
-, P*,N- and P*,P*-Bidentate Diamidophosphites with
-Diazaphospholidine Moieties:
g-
0. – Vol.352 - P. 2599 – 2610.
230 Gavrilov, K.N. Phosphites and diamidophosphites based on
245
–
mono
-ethers of BINOL: a comparison of enantioselectivity in
asymmetric catalytic reactions / K. N. Gavrilov, S. V. Zheglova,
M.N. Gavrilova, I.M. Novikov, M. G. Ma
kin, E.A. Rastorguev, V.A. Davankov // Tetrahedron.
Vol. 68.
hemilabile ligands. / C.S. Slone, D.A. Weinberger, C.A. Mirkin
// Prog. Inorg. Chem.
Acc. Chem. Res.
asymmetric P,N
Sennhenn,H. Steinhagen // Pure Appl. Chem.
No3.
rigid phosphino
Liu, Q. Dai, X.
Article Tetrahedron.
Modular P,N
Pfaltz A. // Acc Chem. Res
new chiral ligands for enantioselective catalysis: Very high
enantioselectivity in palladium catalyzed allylic substitutions /
J.Sprinz, G.Helmchen // Tetrahedr
No11.
Asymmetric Catalysis: Pd
P., Pfaltz A. // Angew. Chem., Int. Ed. Engl.
No9.
tution using phosphorus containing oxazoline ligands / G. J.
Dawson, Ch. G. Frost, J. M.J. Williams, S.J. Coote // Tetrah
dron Letters.
ksimova, N. N. Grosh-
– 2012. –
- P.1581-1589.
231 Slone C.S. The transition metal coordination chemistry of
– 1999. - Vol. 48. – P. 233-350.
232 Crabtree R. Iridium compounds in catalysis / R. Crabtree //
– 1979. – Vol. 12. – No 9. – P. 331-337.
233 Helmchen, G. Enantioselective catalysis with complexes of
-chelate ligands / G. Helmchen, S. Kudis, P.
– 1997. - Vol. 69. -
- P. 513-518.
234 D. Liu A new class of readily available and conformationally
-oxazoline ligands for asymmetric catalysis / D.
Zhang, Q. Dai, X. Zhang // Original Research
– 2005. – Vol. 61. - No26. - P.6460-6471.
235 Helchmen G. PhosphinooxazolinesA New Class of Versatile,
-Ligands for Asymmetric Catalysis / Helchmen G.,
. – 2000. – Vol. 33. – P.336–345.
236 Sprinz J. Phosphinoaryl- and phosphinoalkyloxazolines as
on Lett. – 1993. – Vol. 34. -
– P. 1769-1772.
237 Matt P.Chiral Phosphinoaryldihydrooxazoles as Ligands in
-Catalyzed Allylic Substitution / Matt
– 1993. – Vol.32. -
– P. 566–568.
238 Dawson G. J. Asymmetric palladium catalysed allylic substi-
– 1993. – Vol. 34.- No19. - P. 3149-3150.
239 Coote S. J. The Preparation of Functionalised Aryl Phos-
246
e-
phines from Aryl Fluorides by Nucleophilic Aromatic Substit
u-
tion with Potassium Diphenylphosphide / Coote S. J. Steven J.;
Dawson, Graham J.; Frost, Christopher G.; Williams, Jonathan
M. J. // Synlett
tion of Monosubstituted Allylic Substrates with Phosphinoo
azolines as Ligands. Isolation, Characterization, and Reactivity
of Chiral (Allyl)iridium(III) Complexes / C.Y
F. Rominger, G. Helmchen // Organometallics.
P.5459
Iridium
Schnider, A. Pfaltz // Angew. Chem.
No20.
Phosphino
Catalyzed Asymmetric Hydrogenation / D. Liu, W. Tang, X.
Zhang // Organic
ligands by formation of a P
Tetrahedron Lett.
lyzed by iridium complexes of proline derived phosphine
oxazoline ligands / G. Xu, S. R Gilbertson // Tetrahedron Lett.
2003.
ophene
Enantioselective Pd
mann J. Klaas // Synlett.
asymmetric
Menges F., Kaiser S. // Synlett.
mines using aminophosphino
Blanc, F. Agbossou
1993. - No7. – P.509-510.
240 Yebra, C. Asymmetric Iridium(I)-Catalyzed Allylic Alkyla-
x-
ebra, J. P. Janssen,
– 2004.- Vol.23.-
-5470
241 Lightfoot A. Enantioselective Hydrogenation of Olefins with
–Phosphanodihydrooxazole Catalysts / A.Lightfoot, P.
Int. Ed. – 1998. – Vol.37. –
– P.2897-2899.
242 Liu, D. Synthesis of a New Class of Conformationally Rigid
-oxazolines: Highly Enantioselective Ligands for Ir-
letters. - 2004.- Vol. 6.-No4.- P.513-516.
243 Xu G. Facile synthesis of proline based phosphine-oxazoline
-N bond / G. Xu, S. R Gilbertson //
– 2002. – Vol.43. – No15. – P.2811-2814.
244 Xu G. Asymmetric hydrogenation of aromatic olefins cata-
–
–
– Vol. 44. – P.953- 955.
245 Tietze L.F. Synthesis of Novel Chiral Thiophene-, Benzothi-
- and Benzofuran-Oxazoline Ligands and their Use in the
-Catalyzed Allylation / Tietze L. F., Loh– 2002. – Vol. 12. – P.2083-2085.
246 Cozzi P. G. Iridium-HetPHOX complexes for the catalytic
Hydrogenation of olefins ans imines / Cozzi P. G.,
-2003. – P.833.
247 Blanc, C. Efficient enantioselective hydrogenation of aryli-
-oxazoline iridium catalyst / C.
-Niedercorn, G. Nowogrocki // Tetrahedron:
247
Asymmetry.
– 2004. – Vol.15. – P.2159-2162.
Bohnen, C. Kruger, A. Pfaltz // Chem. Eur. J.
P.887
Liquid/Carbon Dioxide Media / M. Solinas, A. Pfaltz, P.G. Co
zi, W.Leitner // J. Am. Chem. Soc.
P.16142
class of easily prepa
Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz // Adv. Synth.
Catal.
ophene
Enantioselective Pd
mann J. Klaas // Synlett.
asymmetric Hydrogenation of olefins ans imines / P. G
F. Menges, S. Kaiser // Synlett
Oxazoline
McManus, P.J. Guiry // Chem. Rev.
4202.
chiral ligands / N. End, C. Stoessel, U. Berens, P.di Pietroa, P.G.
Cozzia // Tetrahedron: Asymmetry.
2239.
tungsten
Jones, A. Pfaltz // Pure Appl. Chem.
Cata
Chem. Int. Ed.
248 Schnider, P. / P. Schnider, C. Koch, R. Pretot, G. Wans, F.M.
– 1997. – Vol.3. –
-891.
249 Solinas M. Enantioselective Hydrogenation of Imines in Ionic
z-
– 2004. – Vol.126. – No49. –
-16149.
250 Cozzi, P.G. Chiral phosphinopyrrolyl – oxazolines: A new
red, modular P,N – ligands / P.G. Cozzi, N.
– 2001. – Vol.343. – No5.- P.450-454.
251 Tietze L.F. Synthesis of Novel Chiral Thiophene-, Benzothi-
- and Benzofuran-Oxazoline Ligands and their Use in the
-Catalyzed Allylation / Tietze L. F., Loh– 2002. – Vol.12. – P.2083-2085.
252 Cozzi P. G. Iridium-HetPHOX complexes for the catalytic
. Cozzi,
-2003. – Vol.6.- P.833-836.
253 McManus, H.A. Recent Developments in the Application of
-Containing Ligands in Asymmetric Catalysis / H.A.
– 2004. –Vol.104. – P.4151-
254 End, N. HetPHOX: a new class of easily prepared modular
- 2004.- Vol. 15.- P.2235–
255 Pretot, R. Enantio- and regiocontrol in palladium- and
-catalyzed allylic substitutions / R. Pretot, G. C. Lloyd– 1998. – Vol.70. – P. 1035.
256 Pretot, R. New Ligands for Regio- and Enantiocontrol in Pd-
lyzed Allylic Alkylations / R.Pretot, A.Pfaltz // Angew.
– 1998. – Vol. 37.- No3. – P.323–325.
248
257
kylation by addition of lithium iodide / M. Kawatsura,
Y.Uozumi, T.Hayashi // Chem Commun.
heterobidentate ligands with an achiral oxazoline pendant: Sy
thesis and assessment in asymm
Loriga, S. Medici, R.J.Taras // Mol. Catal. A: Chem.
Vol.196.
gands for Asymmetric Heck Reactions / Y. Mata, M. Dieguez,
O.Pamies, C.Claver /
5599.
phosphoroamidite ligands for the copper
1,4
Ruiz, C. Claver // Tetrahedro
No20.
DOL
/ R. Hilgraf, A.Pfaltz // Synlett.
1816.
Ketones with Rhodium
TADDOLate and a Dihydrooxazole Unit / K. Heldmann, D.
Seebach // Helv. Chim. Acta.
1110.
metric catalysis / R. G. Jones, Ch. J. Richards // Tetrahedron
Lett.
Oxazoline Ligands: Ir
tion of Alkenes / J. Blankenstein, A. Pfaltz // Angew. Chem., Int.
Ed.
Kawatsura, M. Regiocontrol in palladium-catalysed allylic al-
– 1998. – P.217.
258 Gladiali, S. Binaphthalene-templated N,S- and N,P-
n-
etric catalysis / S. Gladiali, G.
– 2003. –
– P.27-38.
259 Mata, Y. Chiral Phosphite-oxazolines: A New Class of Li-
/ Org. Lett. – 2005. – Vol.7. – P.5597–
260 Diéguez, M. New chiral amino-phosphite and phosphite-
-catalyzed asymmetric
-addition of diethylzinc to cyclohexenone / M. Diéguez, A.
n: Asymmetry. – 2001. – Vol. 12. –
– P.2861-2866.
261 Hilgraf, R. Chiral Bis(N-tosylamino)phosphine- and TAD-
-Phosphite-Oxazolines as Ligands in Asymmetric Catalysis
– 1999. – Vol.11. – P.1814-
262 Heldmann, D.K. Catalytic Enantioselective Hydrosilylation of
-Phosphite Complexes Containing a
– 1999. – V. 82. – № 7. – P. 1096-
263 Jones, R. G. Simple phosphinite–oxazoline ligands for asym-
– 2001.- Vol.3. - No42. – P.5553-5555.
264 Blankenstein, J. A New Class of Modular Phosphinite–
-Catalyzed Enantioselective Hydrogena-
– 2001. – Vol. 40. – No 23. – P.4445-4447.
249
265
DOL
/ R.
1816.
phosphino derivatives of 2,2
asymmetric catalysis / G.Chelucci, M. A. Cabras, C. Botteghi,
C.Baso
Vol.7.
(diphenylphosphino)methyl
chiral ligand for enantioselective catalysis / G. Chelucci, M.
A.Cabra
–
Catalyzed Reactions / T. Bunlaksananusorn, K. Polborn, P.
Knochel // Angew. Chem.,Int. Ed.
P.3941
Derived from Pyridine and Quinoline / W.J. Drury, N. Zimme
man, M.Keenan, M.Hayashi, S. Kaiser, R.Goddart, A.Pfaltz //
Angew. Chem. Int. Ed.
Chiral Bidentate P,N
)menthoxydiphenylphosphino]pyridine Cationic Rhodium(I)
Complexes / C. G. Arena, F.Nicolo, D. Drommi, G. Bruno F.
Faraone // J. Chem.
2252.
aromatics using a rhodium complex with the (1R,2R,4R)
diphenylphosphinyl
pyridine / Chelucci G., Marchetti
Chem.
phosphorus donor atoms. Syntheses and applications in asymm
Hilgraf, R. Chiral Bis(N-tosylamino)phosphine- and TAD-
-Phosphite-Oxazolines as Ligands in Asymmetric Catalysis
Hilgraf, A.Pfaltz // Synlett. – 1999. – Vol.11. – P.1814-
266 Chelucci, G. Synthesis of homochiral pyridyl, bipyridyl and
-dimethyl-1,3-dioxolane: Use in
li, M. Marchetti // Tetrahedron: Asymmetry. – 1996. –
– No3. – P.885-895.
267 Chelucci, G. (−)-(4S,5R)-4-(2-pyridyl)-5-
-2,2-dimethyl-1,3-dioxolane a new
s, C.Botteghi, M. Marchetti // Tetrahedron: Asymmetry.
1994. – Vol.5. – No 3. – P.299-302.
268 Bunlaksananusorn, T. New P,N Ligands for Asymmetric Ir-
– 2003. – Vol. 42. – No33. –
-3943.
269 Drury, W. J. III Synthesis of Versatile Chiral N,P Ligands
r-
- 2004. – Vol.43. - No1 –P.70-74.
270 Arena, C. G. Enantioselective Hydroformylation with the
-Ligand-2-[1-(1S,2S,5R)-(-
Soc., Chem. Commun. – 1994. – P.2251-
271 Chelucci, G. Enantioselective hydroformylation of vinyl-
-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl)
M., Sechi S. - J. Mol. Cat. A:
– 1997. – Vol. 122. - No2-3. – P.111-114.
272
Cellucci, G. Chiral P,N-ligands with pyridine-nitrogen and
250
-2-(2-
e-
Соседние файлы в предмете [НЕСОРТИРОВАННОЕ]