-
1
-
-
84863825873
-
Charting, navigating, and populating natural products chemical space for drug discovery
-
Lachance H, Wetzel S, Kumar K, Waldmann H. Charting, navigating, and populating natural products chemical space for drug discovery. J Nat Prod 2012; 55: 5989-6001.
-
(2012)
J Nat Prod
, vol.55
, pp. 5989-6001
-
-
Lachance, H.1
Wetzel, S.2
Kumar, K.3
Waldmann, H.4
-
2
-
-
84858308226
-
Natural products as sources of new drugs over the 30 years from 1981 to 2010
-
Newman DJ, Cragg GM. Natural products as sources of new drugs over the 30 years from 1981 to 2010. J Nat Prod 2012; 75: 311-35.
-
(2012)
J Nat Prod
, vol.75
, pp. 311-335
-
-
Newman, D.J.1
Cragg, G.M.2
-
3
-
-
33845370152
-
Styryl lactones and their derivatives: Biological activities, mechanisms of action and potential leads for drug design
-
De Fátima A, Modolo LV, Conegero LS, et al. Styryl lactones and their derivatives: biological activities, mechanisms of action and potential leads for drug design. Curr Med Chem 2006; 13: 3371-84.
-
(2006)
Curr Med Chem
, vol.13
, pp. 3371-3384
-
-
De Fátima, A.1
Modolo, L.V.2
Conegero, L.S.3
-
5
-
-
77953685524
-
The odyssey of marine pharmaceuticals: A current pipeline perspective
-
Mayer AMS, Glaser KB, Cuevas C, et al. The odyssey of marine pharmaceuticals: a current pipeline perspective. Trends Pharmacol Sci 2010; 31: 255-65.
-
(2010)
Trends Pharmacol Sci
, vol.31
, pp. 255-265
-
-
Mayer, A.M.S.1
Glaser, K.B.2
Cuevas, C.3
-
6
-
-
83655183058
-
Scalable enantioselective total synthesis of taxanes
-
Mendoza A, Ishihara Y, Baran PS. Scalable enantioselective total synthesis of taxanes. Nat Chem 2012; 4: 21-5.
-
(2012)
Nat Chem
, vol.4
, pp. 21-25
-
-
Mendoza, A.1
Ishihara, Y.2
Baran, P.S.3
-
7
-
-
80052314928
-
Scalable, stereocontrolled total synthesis of (±)-axinellamines A and B
-
Su S, Rodrigues RA, Baran PS. Scalable, stereocontrolled total synthesis of (±)-axinellamines A and B. J Am Chem Soc 2011; 133: 13922-5.
-
(2011)
J Am Chem Soc
, vol.133
, pp. 13922-13925
-
-
Su, S.1
Rodrigues, R.A.2
Baran, P.S.3
-
8
-
-
79957699838
-
Scalable synthesis of cortistatin A and related structures
-
Shi J, Manolikakes G, Yeh CH, et al. Scalable synthesis of cortistatin A and related structures. J Am Chem Soc 2011; 133: 8014-27.
-
(2011)
J Am Chem Soc
, vol.133
, pp. 8014-8027
-
-
Shi, J.1
Manolikakes, G.2
Yeh, C.H.3
-
9
-
-
67649921097
-
Scalable total synthesis and biological evaluation of haouamine A and its atropoisomer
-
Burns NZ, Krylova IN, Hannoush RN, Baran PS. Scalable total synthesis and biological evaluation of haouamine A and its atropoisomer. J Am Chem Soc 2009; 131: 9172-3.
-
(2009)
J Am Chem Soc
, vol.131
, pp. 9172-9173
-
-
Burns, N.Z.1
Krylova, I.N.2
Hannoush, R.N.3
Baran, P.S.4
-
12
-
-
2342501400
-
Galanthamine from snowdrop-the development of a modern drug against Alzheimer's disease from local Caucasian knowledge
-
Heinrich M, Teoh HL. Galanthamine from snowdrop-the development of a modern drug against Alzheimer's disease from local Caucasian knowledge. J Ethnopharmacol 2004; 92: 147-62.
-
(2004)
J Ethnopharmacol
, vol.92
, pp. 147-162
-
-
Heinrich, M.1
Teoh, H.L.2
-
13
-
-
0034598635
-
Taxines: A review of the mechanism and toxicity of yew (Taxus ssp.) alkaloids
-
Wilson CR, Sauer JM, Hooser SB. Taxines: a review of the mechanism and toxicity of yew (Taxus ssp.) alkaloids. Toxicon 2001; 39: 175-85.
-
(2001)
Toxicon
, vol.39
, pp. 175-185
-
-
Wilson, C.R.1
Sauer, J.M.2
Hooser, S.B.3
-
14
-
-
79955561789
-
Mayapple: A review of the literature from a horticultural perspective
-
Maqbool M. Mayapple: a review of the literature from a horticultural perspective. J Med Plants Res 2011; 5: 1037-45.
-
(2011)
J Med Plants Res
, vol.5
, pp. 1037-1045
-
-
Maqbool, M.1
-
15
-
-
0001635377
-
Podophyllotoxin derivatives: Drug discovery and development
-
Bohlin L, Rosén B. Podophyllotoxin derivatives: drug discovery and development. DDT 1996; 1: 343-51.
-
(1996)
DDT
, vol.1
, pp. 343-351
-
-
Bohlin, L.1
Rosén, B.2
-
16
-
-
0033817918
-
Naturally occuring antinociceptive substances from plants
-
Calixto JB, Beirith A, Ferreira J, Santos ARS, Filho VC, Yunes RA. Naturally occuring antinociceptive substances from plants. Phytother Res 2000; 14: 401-18.
-
(2000)
Phytother Res
, vol.14
, pp. 401-418
-
-
Calixto, J.B.1
Beirith, A.2
Ferreira, J.3
Santos, A.R.S.4
Filho, V.C.5
Yunes, R.A.6
-
18
-
-
0036023387
-
Galantamine-a novel cholinergic drug with a unique dual mode of action for the treatment of patients with Alzheimer's disease
-
Lilienfeld S. Galantamine-a novel cholinergic drug with a unique dual mode of action for the treatment of patients with Alzheimer's disease. CNS Drug Rev 2002; 8: 159-76.
-
(2002)
CNS Drug Rev
, vol.8
, pp. 159-176
-
-
Lilienfeld, S.1
-
21
-
-
34249325470
-
Stereocontrolled synthesis of (-)-galanthamine
-
Satcharoen V, McLean NJ, Kemp SC, Camp NP, Brown RCD. Stereocontrolled synthesis of (-)-galanthamine. Org Lett 2007; 9: 1867-9.
-
(2007)
Org Lett
, vol.9
, pp. 1867-1869
-
-
Satcharoen, V.1
McLean, N.J.2
Kemp, S.C.3
Camp, N.P.4
Brown, R.C.D.5
-
22
-
-
0018255169
-
Stereochemical studies. LIV. A biogenetic-type asymmetric synthesis of optically active galanthamine from L-tyrosine
-
Shimizu K, Tomioka K, Yamada SI, Koga K. Stereochemical studies. LIV. A biogenetic-type asymmetric synthesis of optically active galanthamine from L-tyrosine. Chem Pharm Bull 1978; 26: 3765-71.
-
(1978)
Chem Pharm Bull
, vol.26
, pp. 3765-3771
-
-
Shimizu, K.1
Tomioka, K.2
Yamada, S.I.3
Koga, K.4
-
23
-
-
37049065522
-
Phenol ocidation and biosynthesis Part V. The synthesis of galanthamine
-
Barton DHR, Kirby GW. Phenol ocidation and biosynthesis. Part V. The synthesis of galanthamine. J Chem Soc 1962; 806-17.
-
(1962)
J Chem Soc
, pp. 806-817
-
-
Barton, D.H.R.1
Kirby, G.W.2
-
24
-
-
77951857210
-
Total synthesis of ([)-galanthamine via C3-selective Stille coupling and IMDA cycloaddition cascade of 3, 5-dibromo-2-pyrone
-
Chang JH, Kang HU, Jung IH, Cho CG. Total synthesis of ([)-galanthamine via C3-selective Stille coupling and IMDA cycloaddition cascade of 3, 5-dibromo-2-pyrone. Org Lett 2010; 12: 2016-8.
-
(2010)
Org Lett
, vol.12
, pp. 2016-2018
-
-
Chang, J.H.1
Kang, H.U.2
Jung, I.H.3
Cho, C.G.4
-
25
-
-
33646456628
-
Total synthesis of (.)-galanthamine
-
Hu XD, Tu YQ, Zhang E, et al. Total synthesis of (.)-galanthamine. Org Lett 2006; 8: 1823-5.
-
(2006)
Org Lett
, vol.8
, pp. 1823-1825
-
-
Hu, X.D.1
Tu, Y.Q.2
Zhang, E.3
-
26
-
-
34547700961
-
Total synthesis of (+)-galanthamine starting from D-glucose
-
Tanimoto H, Kato T, Chida N. Total synthesis of (+)-galanthamine starting from D-glucose. Tetrahedron Lett 2007; 48: 6267-70.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 6267-6270
-
-
Tanimoto, H.1
Kato, T.2
Chida, N.3
-
27
-
-
85189258242
-
-
RE41366
-
Thal C, Guillou C, Beunard JL, Gras E, Potier P. Total synthesis of galanthamine analogues and derivatives thereof. RE41366, 2010.
-
(2010)
Total synthesis of galanthamine analogues and derivatives thereof
-
-
Thal, C.1
Guillou, C.2
Beunard, J.L.3
Gras, E.4
Potier, P.5
-
28
-
-
0037008170
-
An efficient enantioselective synthesis of (-)-galanthamine
-
Trost BM, Tang W. An efficient enantioselective synthesis of (-)-galanthamine. Angew Chem Int Ed 2002; 41: 2795-7.
-
(2002)
Angew Chem Int Ed
, vol.41
, pp. 2795-2797
-
-
Trost, B.M.1
Tang, W.2
-
29
-
-
0034669655
-
Enantioselective total synthesis of (-)-galanthamine
-
Trost BM, Toste FD. Enantioselective total synthesis of (-)-galanthamine. J Am Chem Soc 2000; 122: 11262-3.
-
(2000)
J Am Chem Soc
, vol.122
, pp. 11262-11263
-
-
Trost, B.M.1
Toste, F.D.2
-
30
-
-
84861838551
-
Total synthesis of (-)-galanthamine and (-)-lycoramine via catalytic asymmetric hydrogenation and intramolecular reductive Heck cyclization
-
Chen JQ, Xie JH, Bao DH, Liu S, Zhou QL. Total synthesis of (-)-galanthamine and (-)-lycoramine via catalytic asymmetric hydrogenation and intramolecular reductive Heck cyclization. Org Lett 2012; 14: 2714-7.
-
(2012)
Org Lett
, vol.14
, pp. 2714-2717
-
-
Chen, J.Q.1
Xie, J.H.2
Bao, D.H.3
Liu, S.4
Zhou, Q.L.5
-
31
-
-
4544268833
-
Total synthesis of (-)-galanthamine by remote asymmetric induction
-
Kodama S, Hamashima Y, Nishide K, Node M. Total synthesis of (-)-galanthamine by remote asymmetric induction. Angew Chem Int Ed 2004; 43: 2659-61.
-
(2004)
Angew Chem Int Ed
, vol.43
, pp. 2659-2661
-
-
Kodama, S.1
Hamashima, Y.2
Nishide, K.3
Node, M.4
-
32
-
-
0037903823
-
Trommsdorff's
-
Sertüner FW. Trommsdorff's. J Pharmazie 1805; 13: 234.
-
(1805)
J Pharmazie
, vol.13
, pp. 234
-
-
Sertüner, F.W.1
-
34
-
-
84855932564
-
Synthesis of Morphine Alkaloids and Derivatives
-
Rinner U, Hudlicky T. Synthesis of Morphine Alkaloids and Derivatives. Top Curr Chem 2012; 309: 33-66.
-
(2012)
Top Curr Chem
, vol.309
, pp. 33-66
-
-
Rinner, U.1
Hudlicky, T.2
-
35
-
-
33947469818
-
The Synthesis of Morphine
-
Gates M, Tschudi G. The Synthesis of Morphine. J Am Chem Soc 1952; 78: 1380-93.
-
(1952)
J Am Chem Soc
, vol.78
, pp. 1380-1393
-
-
Gates, M.1
Tschudi, G.2
-
37
-
-
0001146788
-
Tandem Reacions in Organic Synthesis: Novel Strategies for Natural Product Elaboration and the Development of New Synthetic Methodology
-
Parsons PJ, Penkett CS, Shell AJ. Tandem Reacions in Organic Synthesis: Novel Strategies for Natural Product Elaboration and the Development of New Synthetic Methodology. Chem Rev 1996; 96: 195-206.
-
(1996)
Chem Rev
, vol.96
, pp. 195-206
-
-
Parsons, P.J.1
Penkett, C.S.2
Shell, A.J.3
-
38
-
-
0030837809
-
Asymmetric Synthesis of (+)-Morphine. The Phenanthrene Route Revisited
-
White JD, Hrnciar P, Stappenbeck F. Asymmetric Synthesis of (+)-Morphine. The Phenanthrene Route Revisited. J Org Chem 1997; 62: 5250-1.
-
(1997)
J Org Chem
, vol.62
, pp. 5250-5251
-
-
White, J.D.1
Hrnciar, P.2
Stappenbeck, F.3
-
41
-
-
0001304372
-
Studies in the (+)-morphinan Series I. An alternate conversion of (+)-dihydrocodeinone into (+)-codeine
-
Rice KC, Iijima I. Studies in the (+)-morphinan Series I. An alternate conversion of (+)-dihydrocodeinone into (+)-codeine. Heterocycles 1977; 6: 1157-65.
-
(1977)
Heterocycles
, vol.6
, pp. 1157-1165
-
-
Rice, K.C.1
Iijima, I.2
-
42
-
-
0017354485
-
A Rapid, high-yield Conversion of Codeine to Morphine
-
Rice KC. A Rapid, high-yield Conversion of Codeine to Morphine. J Med Chem 1977; 20: 164-5.
-
(1977)
J Med Chem
, vol.20
, pp. 164-165
-
-
Rice, K.C.1
-
43
-
-
0000221405
-
Synthetic Opium Alkaloids and Derivatives. A Short Total Synthesis of (±)-Dihydrothebainone, (±)-Dihydrocodeinone, and (±)-Nordihydrocodeinone as an Approach to a Practical Synthesis of Morphine, Codeine, and Congeners
-
Rice KC. Synthetic Opium Alkaloids and Derivatives. A Short Total Synthesis of (±)-Dihydrothebainone, (±)-Dihydrocodeinone, and (±)-Nordihydrocodeinone as an Approach to a Practical Synthesis of Morphine, Codeine, and Congeners. J Org Chem 1980; 45: 3135-7.
-
(1980)
J Org Chem
, vol.45
, pp. 3135-3137
-
-
Rice, K.C.1
-
45
-
-
0015211527
-
Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia
-
Wani MC, Taylor HL, Wall ME, Coggon P, McPhail AT. Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. J Am Chem Soc 1971; 93: 2325-7.
-
(1971)
J Am Chem Soc
, vol.93
, pp. 2325-2327
-
-
Wani, M.C.1
Taylor, H.L.2
Wall, M.E.3
Coggon, P.4
McPhail, A.T.5
-
46
-
-
19044390853
-
Novos produtos naturais capazes de atuar na estabilização de microtúbulos, um importante alvo no combate ao câncer
-
De Souza MVN. Novos produtos naturais capazes de atuar na estabilização de microtúbulos, um importante alvo no combate ao câncer. Quim Nova 2004; 27: 308-12.
-
(2004)
Quim Nova
, vol.27
, pp. 308-312
-
-
De Souza, M.V.N.1
-
47
-
-
34347335758
-
Strategies to bypass the Taxol problem. Enantioselective cascade catalysis, a new approach for the efficient construction of molecular complexity
-
Walji AM, MacMillan DWC. Strategies to bypass the Taxol problem. Enantioselective cascade catalysis, a new approach for the efficient construction of molecular complexity. Synlett 2007; 10: 1477-89.
-
(2007)
Synlett
, vol.10
, pp. 1477-1489
-
-
Walji, A.M.1
McMillan, D.W.C.2
-
49
-
-
24444452269
-
Taxol: Da descoberta ao uso terapêutico
-
Corrêa AG. Taxol: Da descoberta ao uso terapêutico. Quim Nova 1995; 18: 460-7.
-
(1995)
Quim Nova
, vol.18
, pp. 460-467
-
-
Corrêa, A.G.1
-
50
-
-
0028353983
-
First total synthesis of Taxol. 2. Completion of the C and Drings
-
Holton RA, Kim H, Somoza C, et al. First total synthesis of Taxol. 2. Completion of the C and D rings. J Am Chem Soc 1994; 116: 1599-1600.
-
(1994)
J Am Chem Soc
, vol.116
, pp. 1599-1600
-
-
Holton, R.A.1
Kim, H.2
Somoza, C.3
-
51
-
-
0028868994
-
Total synthesis of Taxol. 4. The final stages and completion of the synthesis
-
Nicolaou KC, Ueno H, Liu JJ, et al. Total synthesis of Taxol. 4. The final stages and completion of the synthesis. J Am Chem Soc 1995; 117: 653-9.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 653-659
-
-
Nicolaou, K.C.1
Ueno, H.2
Liu, J.J.3
-
53
-
-
0030936927
-
The pinene path to Taxanes. 6. A concise stereocontrolled synthesis of Taxol
-
Wender PA, Badham NF, Conway SP, et al. The pinene path to Taxanes. 6. A concise stereocontrolled synthesis of Taxol. J Am Chem Soc 1997; 119: 2757-8.
-
(1997)
J Am Chem Soc
, vol.119
, pp. 2757-2758
-
-
Wender, P.A.1
Badham, N.F.2
Conway, S.P.3
-
54
-
-
0032539249
-
Enantioselective total synthesis of Taxol
-
Morihira K, Hara R, Kawahara S, et al. Enantioselective total synthesis of Taxol. J Am Chem Soc 1998; 120: 12980-1.
-
(1998)
J Am Chem Soc
, vol.120
, pp. 12980-12981
-
-
Morihira, K.1
Hara, R.2
Kawahara, S.3
-
55
-
-
0028213668
-
First total synthesis of Taxol. 1. Functionalization of the B ring
-
Holton RA, Kim H, Somoza C, et al. First total synthesis of Taxol. 1. Functionalization of the B ring. J Am Chem Soc 1994; 116: 1597-8.
-
(1994)
J Am Chem Soc
, vol.116
, pp. 1597-1598
-
-
Holton, R.A.1
Kim, H.2
Somoza, C.3
-
61
-
-
0028810338
-
Total synthesis of Taxol. 1. Retrosynthesis, degradation, and reconstitution
-
Nicolaou KC, Nantermet PG, Ueno H, Guy RK, Couladouros EA, Sorensen EJ. Total synthesis of Taxol. 1. Retrosynthesis, degradation, and reconstitution. J Am Chem Soc 1995; 117: 624-33.
-
(1995)
J Am Chem Soc
, vol.117
, pp. 624-633
-
-
Nicolaou, K.C.1
Nantermet, P.G.2
Ueno, H.3
Guy, R.K.4
Couladouros, E.A.5
Sorensen, E.J.6
-
62
-
-
33947454394
-
Components of podophyllin. XVI. Podophyllotoxin haloacetates and quaternary derivatives
-
Schrecker AW, Greenberg GY, Hartwell JL. Components of podophyllin. XVI. Podophyllotoxin haloacetates and quaternary derivatives. J Am Chem Soc 1954; 76: 1184-5.
-
(1954)
J Am Chem Soc
, vol.76
, pp. 1184-1185
-
-
Schrecker, A.W.1
Greenberg, G.Y.2
Hartwell, J.L.3
-
63
-
-
0033083666
-
Lignans, neolignans and related compounds
-
Ward RS. Lignans, neolignans and related compounds. Nat Prod Rep 1999; 16: 75-96.
-
(1999)
Nat Prod Rep
, vol.16
, pp. 75-96
-
-
Ward, R.S.1
-
64
-
-
0031810637
-
Podophylltoxins: Current status and recent developments
-
Damayanthi Y, Lown JW. Podophylltoxins: Current status and recent developments. Curr Med Chem 1998; 5: 205-52.
-
(1998)
Curr Med Chem
, vol.5
, pp. 205-252
-
-
Damayanthi, Y.1
Lown, J.W.2
-
65
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
Ravelli RBG, Gigant B, Curmi PA, et al. Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain, Nature 2004; 428: 198-202.
-
(2004)
Nature
, vol.428
, pp. 198-202
-
-
Ravelli, R.B.G.1
Gigant, B.2
Curmi, P.A.3
-
66
-
-
79960676884
-
Structural Basis of Type II Topoisomerase Inhibition by the Anticancern Drug Etoposide
-
Wu CC, Li TK, Farh L, et al. Structural Basis of Type II Topoisomerase Inhibition by the Anticancern Drug Etoposide. Science 2011; 333: 459-62.
-
(2011)
Science
, vol.333
, pp. 459-462
-
-
Wu, C.C.1
Li, T.K.2
Farh, L.3
-
67
-
-
60849114785
-
Enantioselective Sequential Conjugate Addition-Allylation Reactions: A Concise Total Synthesis of (+)-Podophyllotoxin
-
Wu Y, Zhao J, Chen J, Pan C, Li L, Zhang H. Enantioselective Sequential Conjugate Addition-Allylation Reactions: A Concise Total Synthesis of (+)-Podophyllotoxin. Org Lett 2009; 11(3): 597-600.
-
(2009)
Org Lett
, vol.11
, Issue.3
, pp. 597-600
-
-
Wu, Y.1
Zhao, J.2
Chen, J.3
Pan, C.4
Li, L.5
Zhang, H.6
-
68
-
-
0013980195
-
Synthesis of Podophyllotoxin
-
Gensler WJ, Gatsonis CD. Synthesis of Podophyllotoxin, J Org Chem 1966; 31: 4004-8.
-
(1966)
J Org Chem
, vol.31
, pp. 4004-4008
-
-
Gensler, W.J.1
Gatsonis, C.D.2
-
69
-
-
0023768503
-
Asymmetric Total Synthesis of (-)-Podophyllotoxin
-
Andrews RC, Teague SJ, Meyers AI. Asymmetric Total Synthesis of (-)-Podophyllotoxin. J Am Chem Soc 1988; 110: 7854-8.
-
(1988)
J Am Chem Soc
, vol.110
, pp. 7854-7858
-
-
Andrews, R.C.1
Teague, S.J.2
Meyers, A.I.3
-
70
-
-
0033960568
-
Enzyme-Assisted Asymmetric Total Synthesis of (-)-Podophyllotoxin and (-)-Picropodophyllin
-
Berkowitz DB, Choi S, Maeng JH. Enzyme-Assisted Asymmetric Total Synthesis of (-)-Podophyllotoxin and (-)-Picropodophyllin. J Org Chem 2000; 65: 847-60.
-
(2000)
J Org Chem
, vol.65
, pp. 847-860
-
-
Berkowitz, D.B.1
Choi, S.2
Maeng, J.H.3
-
73
-
-
0027164889
-
Asymmetric total synthesis of (-)-podophyllotoxin
-
Bush EJ, Jones DW. Asymmetric total synthesis of (-)-podophyllotoxin. J Chem Soc Chem Commun 1993; 1200-1201.
-
(1993)
J Chem Soc Chem Commun
, pp. 1200-1201
-
-
Bush, E.J.1
Jones, D.W.2
-
74
-
-
54749151723
-
Concise Stereoselective Synthesis of (-)-Podophyllotoxin by an Intermolecular Iron(III)-Catalyzed Friedel-Crafts Alkylation
-
Stadler D, Bach T. Concise Stereoselective Synthesis of (-)-Podophyllotoxin by an Intermolecular Iron(III)-Catalyzed Friedel-Crafts Alkylation. Angew Chem Int Ed 2008; 47: 7557-9.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 7557-7559
-
-
Stadler, D.1
Bach, T.2
-
75
-
-
0001135275
-
Asymmetric Tandem Addition to Chiral 1-and 2-Substituted Naphthalenes. Application to the Synthesis of (+)-Phyltetralin
-
Meyers AI, Barner B, Roth G, Hoyer D, Laucher D. Asymmetric Tandem Addition to Chiral 1-and 2-Substituted Naphthalenes. Application to the Synthesis of (+)-Phyltetralin. J Am Chem Soc 1988; 110: 4611-24.
-
(1988)
J Am Chem Soc
, vol.110
, pp. 4611-4624
-
-
Meyers, A.I.1
Barner, B.2
Roth, G.3
Hoyer, D.4
Laucher, D.5
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