-
1
-
-
0022979685
-
Bengamides, heterocyclic anthelminthics from a jaspidae marine sponge
-
Quiñoà, E.; Adamczeski, M.; Crews, P. Bengamides, heterocyclic anthelminthics from a jaspidae marine sponge. J. Org. Chem. 1986, 51, 4497-4498.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 4497-4498
-
-
Quiñoà, E.1
Adamczeski, M.2
Crews, P.3
-
2
-
-
0033403329
-
Cytotoxic metabolites from an Australian collection of the sponge Jaspis species
-
DOI 10.1021/np9902688
-
Groweiss, A.; Newcomer, J.J.; O'Keefe, B.R.; Blackman, A.; Boyd, M.R. Cytotoxic metabolites from an Australian collection of the sponge Jaspis species. J. Nat. Prod. 1999, 62, 1691-1693. (Pubitemid 30030619)
-
(1999)
Journal of Natural Products
, vol.62
, Issue.12
, pp. 1691-1693
-
-
Groweiss, A.1
Newcomer, J.J.2
O'Keefe, B.R.3
Blackman, A.4
Boyd, M.R.5
-
3
-
-
4243562790
-
Jasplakinolide, a cyclodepsipeptide from the marine sponge, Jaspis sp
-
Crews, P.; Manes, L.V.; Boehler, M. Jasplakinolide, a cyclodepsipeptide from the marine sponge, Jaspis sp. Tetrahedron Lett. 1986, 27, 2797-2800.
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 2797-2800
-
-
Crews, P.1
Manes, L.V.2
Boehler, M.3
-
4
-
-
84873162243
-
Advances in the total synthesis of cyclodepsipeptide (+)-Jasplakinolide (Jaspamide) and its analogs
-
Xu, Y.-Y.; Liu, C.; Liu, Z.-P. Advances in the total synthesis of cyclodepsipeptide (+)-Jasplakinolide (Jaspamide) and its analogs. Curr. Org. Synth. 2013, 10, 67-89.
-
(2013)
Curr. Org. Synth.
, vol.10
, pp. 67-89
-
-
Xu, Y.-Y.1
Liu, C.2
Liu, Z.-P.3
-
5
-
-
0008853397
-
Jaspamide from the marine sponge Jaspis johnstoni
-
Braekman, J.C.; Daloze, D.; Moussiaux, B. Jaspamide from the marine sponge Jaspis johnstoni. J. Nat. Prod. 1987, 50, 994-995.
-
(1987)
J. Nat. Prod.
, vol.50
, pp. 994-995
-
-
Braekman, J.C.1
Daloze, D.2
Moussiaux, B.3
-
6
-
-
0033058149
-
New jaspamide derivatives from the marine sponge Jaspis splendans collected in Vanuatu
-
DOI 10.1021/np9803225
-
Zampella, A.; Giannini, C.; Debitus, C.; Roussakis, C.; D'Auria, M.V. New jaspamide derivatives from the marine sponge Jaspis splendans collected in Vanuatu. J. Nat. Prod. 1999, 62, 332-334. (Pubitemid 29137925)
-
(1999)
Journal of Natural Products
, vol.62
, Issue.2
, pp. 332-334
-
-
Zampella, A.1
Giannini, C.2
Debitus, C.3
Roussakis, C.4
D'Auria, M.V.5
-
7
-
-
34247863615
-
New jaspamide derivatives with antimicrofilament activity from the sponge Jaspis splendans
-
DOI 10.1016/j.tet.2007.03.162, PII S004040200700614X
-
Gala, F.; D'Auria, M.V.; de Marino, S.; Zollo, F.; Smith, C.D.; Copper, J.E.; Zampella, A. New jaspamide derivatives with antimicrofilament activity from the sponge Jaspis splendans. Tetrahedron 2007, 63, 5212-5219. (Pubitemid 46702221)
-
(2007)
Tetrahedron
, vol.63
, Issue.24
, pp. 5212-5219
-
-
Gala, F.1
D'Auria, M.V.2
De Marino, S.3
Zollo, F.4
Smith, C.D.5
Copper, J.E.6
Zampella, A.7
-
8
-
-
45449105944
-
Jaspamides H-L, new actin-targeting depsipeptides from the sponge Jaspis splendans
-
Gala, F.; D'Auria, M.V.; de Marino, S.; Sepe, V.; Zollo, F.; Smith, C.D.; Copper, J.E.; Zampella, A. Jaspamides H-L, new actin-targeting depsipeptides from the sponge Jaspis splendans. Tetrahedron 2008, 64, 7127-7130.
-
(2008)
Tetrahedron
, vol.64
, pp. 7127-7130
-
-
Gala, F.1
D'Auria, M.V.2
De Marino, S.3
Sepe, V.4
Zollo, F.5
Smith, C.D.6
Copper, J.E.7
Zampella, A.8
-
9
-
-
56949095877
-
Jaspamides M-P: New tryptophan modified jaspamide derivatives from the sponge Jaspis splendans
-
Gala, F.; D'Auria, M.V.; de Marino, S.; Sepe, V.; Zollo, F.; Smith, C.D.; Keller, S.N.; Zampella, A. Jaspamides M-P: New tryptophan modified jaspamide derivatives from the sponge Jaspis splendans. Tetrahedron 2009, 65, 51-56.
-
(2009)
Tetrahedron
, vol.65
, pp. 51-56
-
-
Gala, F.1
D'Auria, M.V.2
De Marino, S.3
Sepe, V.4
Zollo, F.5
Smith, C.D.6
Keller, S.N.7
Zampella, A.8
-
10
-
-
33845184916
-
Novel sponge-derived amino acids. 5. Structures, stereochemistry, and synthesis of several new heterocycles
-
Adamczeski, M.; Quiñoà, E.; Crews, P. Novel sponge-derived amino acids. 5. Structures, stereochemistry, and synthesis of several new heterocycles. J. Am. Chem. Soc. 1989, 111, 647-654.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 647-654
-
-
Adamczeski, M.1
Quiñoà, E.2
Crews, P.3
-
11
-
-
0030008240
-
Jaspiferals A-G, new cytotoxic isomalabaricane-type nortriterpenoids from okinawan marine sponge Jaspis stellifera
-
Kobayashi, J.; Yuasa, K.; Kobayashi, T.; Sasaki, T.; Tsuda, M. Jaspiferals A-G, new cytotoxic isomalabaricane-type nortriterpenoids from okinawan marine sponge Jaspis stellifera. Tetrahedron 1996, 52, 5745-5750.
-
(1996)
Tetrahedron
, vol.52
, pp. 5745-5750
-
-
Kobayashi, J.1
Yuasa, K.2
Kobayashi, T.3
Sasaki, T.4
Tsuda, M.5
-
12
-
-
0026022356
-
Stelliferins A-F, new antineoplastic isomalabaricane triterpenes from the Okinawan marine sponge Jaspis stellifera
-
Tsuda, M.; Ishibashi, M.; Agemi, K.; Sasaki, T.; Kobayashi, J. Stelliferins A-F, new antineoplastic isomalabaricane triterpenes from the Okinawan marine sponge Jaspis stellifera. Tetrahedron 1991, 47, 2181-2194.
-
(1991)
Tetrahedron
, vol.47
, pp. 2181-2194
-
-
Tsuda, M.1
Ishibashi, M.2
Agemi, K.3
Sasaki, T.4
Kobayashi, J.5
-
13
-
-
17544363911
-
New isomalabaricane derivatives from a new species of Jaspis sponge collected at the Vanuatu islands
-
Zampella, A.; D'Auria, M.V.; Debitus, C.; Menou, J.L. New isomalabaricane derivatives from a new species of Jaspis sponge collected at the Vanuatu islands. J. Nat. Prod. 2000, 63, 943-946.
-
(2000)
J. Nat. Prod.
, vol.63
, pp. 943-946
-
-
Zampella, A.1
D'Auria, M.V.2
Debitus, C.3
Menou, J.L.4
-
14
-
-
0035091235
-
New cytotoxic isomalabaricane triterpenes from the sponge Jaspis species
-
DOI 10.1021/np000478g
-
Meragelman, K.M.; McKee, T.C.; Boyd, M.R. New cytotoxic isomalabaricane triterpenes from the sponge Jaspis species. J. Nat. Prod. 2001, 64, 389-392. (Pubitemid 32249814)
-
(2001)
Journal of Natural Products
, vol.64
, Issue.3
, pp. 389-392
-
-
Meragelman, K.M.1
McKee, T.C.2
Boyd, M.R.3
-
15
-
-
0027270461
-
Jaspisamides A-C, new cytotoxic macrolides from the Okinawan sponge Jaspis sp
-
Kobayashi, J.; Murata, O.; Shigemori, H. Jaspisamides A-C, new cytototic macrolides from the okinawan sponge Jaspis sp. J. Nat. Prod. 1993, 566, 787-791. (Pubitemid 23170743)
-
(1993)
Journal of Natural Products (Lloydia)
, vol.56
, Issue.5
, pp. 787-791
-
-
Kobayashi, J.1
Murata, O.2
Shigemori, H.3
Sasaki, T.4
-
16
-
-
0028149744
-
3,4-Dihydroxystyrene dimers, inducers of larval metamorphosis in ascidians, from a marine sponge Jaspis sp.
-
DOI 10.1016/S0040-4020(01)85673-8
-
Tsukamoto, S.; Kato, H.; Hirota, H.; Fusetani, N. 3,4-Dihydroxystyrene dimers, inducers of larval metamorphosis in Ascidians, from a marine sponge Jaspis sp. Tetrahedron 1994, 50, 13583-13592. (Pubitemid 24355269)
-
(1994)
Tetrahedron
, vol.50
, Issue.48
, pp. 13583-13592
-
-
Tsukamoto, S.1
Kato, H.2
Hirota, H.3
Fusetani, N.4
-
17
-
-
0028064418
-
Narains: N, N-dimethylguanidinium styryl sulfates, metamorphosis inducers of Ascidian Larvae from a marine sponge Jaspis sp
-
Tsukamoto, S.; Kato, H.; Hirota, H.; Fusetani, N. Narains: N, N-dimethylguanidinium styryl sulfates, metamorphosis inducers of Ascidian Larvae from a marine sponge Jaspis sp. Tetrahedron Lett. 1994, 35, 5873-5874.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 5873-5874
-
-
Tsukamoto, S.1
Kato, H.2
Hirota, H.3
Fusetani, N.4
-
18
-
-
0024947413
-
The isolation and structure of modified bioactive nucleosides from Jaspis johnstoni
-
Zabriskie, T.M.; Ireland, C.M. The isolation and structure of modified bioactive nucleosides from Jaspis johnstoni. J. Nat. Prod. 1989, 52, 1353-1356. (Pubitemid 20101797)
-
(1989)
Journal of Natural Products (Lloydia)
, vol.52
, Issue.6
, pp. 1353-1356
-
-
Zabriskie, T.M.1
Ireland, C.M.2
-
19
-
-
0037420988
-
Jaspines A and B: Two new cytotoxic sphingosine derivatives from the marine sponge Jaspis sp.
-
DOI 10.1016/S0040-4039(02)02541-8, PII S0040403902025418
-
Ledroit, V.; Debitus, C.; Lavaud, C.; Massiot, G. Jaspines A and B: Two new cytotoxic sphingosine derivatives from the marine sponge Jaspis sp. Tetrahedron Lett. 2003, 44, 225-228. (Pubitemid 35449550)
-
(2003)
Tetrahedron Letters
, vol.44
, Issue.2
, pp. 225-228
-
-
Ledroit, V.1
Debitus, C.2
Lavaud, C.3
Massiot, G.4
-
20
-
-
0035831239
-
Bengamides revisited: New structures and antitumor studies
-
DOI 10.1021/jo001380+
-
Thale, Z.; Kinder, F.R.; Bair, K.W.; Bontempo, J.; Czuchta, A.M.; Versace, R.W.; Phillips, P.E.; Sanders, M.L.; Wattanasin, S.; Crews, P. Bengamides revisited: New structures and antitumor studies. J. Org. Chem. 2001, 66, 1733-1741. (Pubitemid 32205111)
-
(2001)
Journal of Organic Chemistry
, vol.66
, Issue.5
, pp. 1733-1741
-
-
Thale, Z.1
Kinder, F.R.2
Bair, K.W.3
Bontempo, J.4
Czuchta, A.M.5
Versace, R.W.6
Phillips, P.E.7
Sanders, M.L.8
Wattanasin, S.9
Crews, P.10
-
21
-
-
0030796456
-
Bengamides and related new amino acid derivatives from the new caledonian marine sponge Jaspis carteri
-
DOI 10.1021/np970050q
-
D'Auria, M.V.; Giannini, C.; Minale, L.; Zampella, A.; Debitus, C.; Frostin, M. Bengamides and related new amino acid derivatives from the new caledonian marine sponge Jaspis carteri. J. Nat. Prod. 1997, 60, 814-816. (Pubitemid 27372011)
-
(1997)
Journal of Natural Products
, vol.60
, Issue.8
, pp. 814-816
-
-
D'Auria, M.V.1
Giannini, C.2
Minale, L.3
Zampella, A.4
Debitus, C.5
Frostin, M.6
-
22
-
-
0027937370
-
Amino acid derivatives from the marine sponge Jaspis digonoxea
-
DOI 10.1021/np50108a023
-
Rudi, A.; Kashman, Y. Amino acid derivatives from the marine sponge Jaspis digonoxea. J. Nat. Prod. 1994, 57, 829-832. (Pubitemid 24249327)
-
(1994)
Journal of Natural Products
, vol.57
, Issue.6
, pp. 829-832
-
-
Rudi, A.1
Kashman, Y.2
Benayahu, Y.3
Schleyer, M.4
-
23
-
-
0027476582
-
Developments in marine natural products: Receptor- specific bioactive compounds
-
Molinski, T.F. Developments in marine natural products. Receptor-specific bioactive compounds. J. Nat. Prod. 1993, 56, 1-8. (Pubitemid 23066671)
-
(1993)
Journal of Natural Products (Lloydia)
, vol.56
, Issue.1
, pp. 1-8
-
-
Molinski, T.F.1
-
24
-
-
0028272318
-
Isojaspisin: A novel styryl sulfate from a marine sponge, Jaspis sp., that inhibits hatching of sea urchin embryos
-
DOI 10.1016/S0040-4039(00)60734-7
-
Ohta, S.; Kobayashi, H.; Ikegami, S. Isojaspisin: A novel styryl sulfate from a marine sponge, Jaspis sp., that inhibits hatching of sea urchin embryos. Tetrahedron Lett. 1994, 35, 4579-4580. (Pubitemid 24203132)
-
(1994)
Tetrahedron Letters
, vol.35
, Issue.26
, pp. 4579-4580
-
-
Ohta, S.1
Kobayashi, H.2
Ikegami, S.3
-
25
-
-
0029953345
-
Bengazoles C-G from the sponge Jaspis sp. Synthesis of the side chain and determination of absolute configuration
-
DOI 10.1021/jo952261a
-
Searle, P.A.; Richter, R.K.; Molinski, T.F. Bengazoles C-G from the sponge Jaspis sp. synthesis of the side chain and determination of absolute configuration. J. Org. Chem. 1996, 66, 4073-4079. (Pubitemid 26201409)
-
(1996)
Journal of Organic Chemistry
, vol.61
, Issue.12
, pp. 4073-4079
-
-
Searle, P.A.1
Richter, R.K.2
Molinski, T.F.3
-
26
-
-
0142042908
-
A new cytotoxic and tubulin-interactive milnamide derivative from a marine sponge Cymbastela sp.
-
DOI 10.1021/ol035476c
-
Chevallier, C.; Richardson, A.D.; Edler, M.C.; Hamel, E.; Harper, M.K.; Ireland, C.M. A new cytotoxic and tubulin-interactive milnamide derivative from a marine sponge Cymbastela sp. Org. Lett. 2003, 5, 3737-3739. (Pubitemid 37289568)
-
(2003)
Organic Letters
, vol.5
, Issue.20
, pp. 3737-3739
-
-
Chevallier, C.1
Richardson, A.D.2
Edler, M.C.3
Hamel, E.4
Harper, M.K.5
Ireland, C.M.6
-
27
-
-
82655168247
-
A new diketopiperazine, cyclo-(4-S-hydroxy-R-proline-R-isoleucine), from an Australian specimen of the sponge Stelletta sp
-
Ovenden, S.P.; Nielson, J.L.; Liptrot, C.H.; Willis, R.H.; Tapiolas, D.M.; Wright, A.D.; Motti, C.A. A new diketopiperazine, cyclo-(4-S-hydroxy-R- proline-R-isoleucine), from an Australian specimen of the sponge Stelletta sp. Mar. Drugs 2011, 9, 2469-2478.
-
(2011)
Mar. Drugs
, vol.9
, pp. 2469-2478
-
-
Ovenden, S.P.1
Nielson, J.L.2
Liptrot, C.H.3
Willis, R.H.4
Tapiolas, D.M.5
Wright, A.D.6
Motti, C.A.7
-
28
-
-
84863206712
-
Myxobacteria versus sponge-derived alkaloids: The bengamide family identified as potent immune modulating agents by scrutiny of LC-MS/ELSD libraries
-
Johnson, T.A.; Sohn, J.; Vaske, Y.M.; White, K.N.; Cohen, T.L.; Vervoort, H.C.; Tenney, K.; Valeriote, F.A.; Bjeldanes, L.F.; Crews, P. Myxobacteria versus sponge-derived alkaloids: The bengamide family identified as potent immune modulating agents by scrutiny of LC-MS/ELSD libraries. Bioorg. Med. Chem. 2012, 20, 4348-4355.
-
(2012)
Bioorg. Med. Chem.
, vol.20
, pp. 4348-4355
-
-
Johnson, T.A.1
Sohn, J.2
Vaske, Y.M.3
White, K.N.4
Cohen, T.L.5
Vervoort, H.C.6
Tenney, K.7
Valeriote, F.A.8
Bjeldanes, L.F.9
Crews, P.10
-
29
-
-
0038270061
-
Antifungal metabolites from the marine sponge Pachastrissa sp.: New bengamide and bengazole derivatives
-
DOI 10.1021/np980330l
-
Fernández, R.; Dherbomez, M.; Letourneux, Y.; Nabil, M.; Verbist, J.F.; Biard, J.F. Antifungal metabolites from the marine sponge Pachastrissa sp.: New bengamide and bengazole derivatives. J. Nat. Prod. 1999, 62, 678-680. (Pubitemid 29259078)
-
(1999)
Journal of Natural Products
, vol.62
, Issue.5
, pp. 678-680
-
-
Fernandez, R.1
Dherbomez, M.2
Letourneux, Y.3
Nabil, M.4
Verbist, J.F.5
Biard, J.F.6
-
30
-
-
79960934531
-
Stelliferins J-N, isomalabaricane-type triterpenoids from Okinawan marine sponge Rhabdastrella cf. globostellata
-
Tanaka, N.; Momose, R.; Shibazaki, A.; Gonoi, T.; Fromont, J.; Kobayashi, J. Stelliferins J-N, isomalabaricane-type triterpenoids from Okinawan marine sponge Rhabdastrella cf. globostellata. Tetrahedron 2011, 67, 6689-6696.
-
(2011)
Tetrahedron
, vol.67
, pp. 6689-6696
-
-
Tanaka, N.1
Momose, R.2
Shibazaki, A.3
Gonoi, T.4
Fromont, J.5
Kobayashi, J.6
-
31
-
-
0342614927
-
New isomalabaricane triterpenes from the marine sponge Stelletta globostellata that induce morphological changes in rat fibroblasts
-
DOI 10.1021/np990333d
-
Oku, N.; Matsunaga, S.; Wada, S.; Watabe, S.; Fusetani, N. New isolabaricane triterpenes from the marine sponge Stelleta. globostellata that induce morphological changes in rat fibroblasts. J. Nat. Prod. 2000, 63, 205-209. (Pubitemid 30126921)
-
(2000)
Journal of Natural Products
, vol.63
, Issue.2
, pp. 205-209
-
-
Naoya, O.1
Matsunaga, S.2
Wada, S.-I.3
Watabe, S.4
Fusetani, N.5
-
32
-
-
0034973601
-
Stelliferin riboside, a triterpene monosaccharide isolated from the Fijian sponge Geodia globostellifera
-
DOI 10.1021/np010019v
-
Tabudravu, J.N.; Jaspars, M. Stelliferin riboside, a tritepene monosaccharide isolated from the Fijian sponge Geodia globostellifera. J. Nat. Prod. 2001, 64, 813-815. (Pubitemid 32565939)
-
(2001)
Journal of Natural Products
, vol.64
, Issue.6
, pp. 813-815
-
-
Tabudravu, J.N.1
Jaspars, M.2
-
33
-
-
15044354866
-
Total synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (Jaspine B)
-
DOI 10.1021/ol0473290
-
Bhaket, P.; Morris, K.; Stauffer, C.S.; Datta, A. Total synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine B). Org. Lett. 2005, 7, 875-876. (Pubitemid 40380248)
-
(2005)
Organic Letters
, vol.7
, Issue.5
, pp. 875-876
-
-
Bhaket, P.1
Morris, K.2
Stauffer, C.S.3
Datta, A.4
-
34
-
-
0023866732
-
Unusual anthelminthic oxazoles from a marine sponge
-
Adamczeski, M.; Quiñoà, E.; Crews, P. Unusual anthelminthic oxazoles from a marine sponge. J. Am. Chem. Soc. 1988, 110, 1598-1602. (Pubitemid 18066748)
-
(1988)
Journal of the American Chemical Society
, vol.110
, Issue.5
, pp. 1598-1602
-
-
Adamczeski, M.1
Quinoa, E.2
Crews, P.3
-
35
-
-
0027167775
-
Novel cytotoxic topoisomerase II inhibiting pyrroloiminoquinones from Fijian sponges of the genus Zyzzya
-
Radisky, D.C.; Radisky, E.S.; Barrows, L.R.; Copp, B.R.; Kramer, R.A.; Ireland, C.M. Novel cytotoxic topoisomerase II inhibiting pyrroloiminoquinones from Fijian sponges of the genus Zyzzya. J. Am. Chem. Soc. 1993, 115, 1632-1638. (Pubitemid 23134849)
-
(1993)
Journal of the American Chemical Society
, vol.115
, Issue.5
, pp. 1632-1638
-
-
Radisky, D.C.1
Radisky, E.S.2
Barrow, L.R.3
Copp, B.R.4
Kramer, R.A.5
Ireland, C.M.6
-
36
-
-
0035142057
-
Laboratory culture of the myxomycetes: Formation of fruiting bodies of Didymium bahiense and its plasmodial production of makaluvamine A
-
DOI 10.1021/np000382m
-
Ishibashi, M.; Iwasaki, T.; Imai, S.; Sakamoto, S.; Yamaguchi, K.; Ito, A. Laboratory culture of the Myomycetes: Formation of fruiting bodies of Didymium bahiense and its plasmodial production of Makaluvamine A. J. Nat. Prod. 2001, 64, 108-110. (Pubitemid 32107792)
-
(2001)
Journal of Natural Products
, vol.64
, Issue.1
, pp. 108-110
-
-
Ishibashi, M.1
Iwasaki, T.2
Imai, S.3
Sakamoto, S.4
Yamaguchi, K.5
Ito, A.6
-
37
-
-
77955699983
-
Chiral sulfur ylides for the synthesis of bengamide E and analogues
-
Sarabia, F.; Martín-Gálvez, F.; Chammaa, S.; Martín-Ortiz, L.; Sánchez-Ruiz, A. Chiral sulfur ylides for the synthesis of bengamide E and analogues. J. Org. Chem. 2010, 75, 5526-5532.
-
(2010)
J. Org. Chem.
, vol.75
, pp. 5526-5532
-
-
Sarabia, F.1
Martín-Gálvez, F.2
Chammaa, S.3
Martín-Ortiz, L.4
Sánchez-Ruiz, A.5
-
38
-
-
0025215027
-
Novel sponge-derived amino acids. 11. The entire absolute stereochemistry of the bengamides
-
Adamczeski, M.; Quiñoà, E.; Crews, P. Novel sponge-derived amino acids. 11. The entire absolute stereochemistry of the bengamides. J. Org. Chem. 1990, 55, 240-242. (Pubitemid 20094847)
-
(1990)
Journal of Organic Chemistry
, vol.55
, Issue.1
, pp. 240-242
-
-
Adamczeski, M.1
Quinoa, E.2
Crews, P.3
-
39
-
-
33947085552
-
Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α- trifluoromethylphenylacetate (MTPA) esters
-
Dale, J.A.; Mosher, H.S. Nuclear magnetic resonance enantiomer reagents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α- trifluoromethylphenylacetate (MTPA) esters. J. Am. Chem. Soc. 1973, 95, 512-519.
-
(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 512-519
-
-
Dale, J.A.1
Mosher, H.S.2
-
40
-
-
0026690381
-
Total synthesis and absolute configuration of bengamide A
-
doi:10.1039/C39920001064
-
Chida, N.; Tobe, T.; Okada, S.; Ogawa, S. Total synthesis and absolute configuration of bengamide A. J. Chem. Soc. Chem. Commun. 1992, 1064-1066; doi:10.1039/C39920001064.
-
(1992)
J. Chem. Soc. Chem. Commun.
, pp. 1064-1066
-
-
Chida, N.1
Tobe, T.2
Okada, S.3
Ogawa, S.4
-
41
-
-
0026006752
-
Enantioselective total syntheses of bengamides B and E
-
Broka, C.A.; Ehrler, J. Enantioselective total syntheses of bengamides B and E. Tetrahedron Lett. 1991, 32, 5907-5910.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5907-5910
-
-
Broka, C.A.1
Ehrler, J.2
-
42
-
-
0025978012
-
Total synthesis of bengamide E
-
Chida, N.; Tobe, T.; Ogawa, S. Total synthesis of bengamide E. Tetrahedron Lett. 1991, 32, 1063-1066.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 1063-1066
-
-
Chida, N.1
Tobe, T.2
Ogawa, S.3
-
43
-
-
0000404974
-
Biosynthetic studies of marine lipids. 5. The biosynthesis of long-chain branched fatty acids in marine sponges
-
Carballeira, N.; Thompson, J.E.; Ayanoglu, E.; Djerassi, C. Biosynthetic studies of marine lipids. 5. The biosynthesis of long-chain branched fatty acids in marine sponges. J. Org. Chem. 1986, 51, 2751-2756.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 2751-2756
-
-
Carballeira, N.1
Thompson, J.E.2
Ayanoglu, E.3
Djerassi, C.4
-
44
-
-
33845281820
-
Biosynthetic studies of marine lipids. 11. Synthesis, biosynthesis, and absolute configuration of the internally branched demospongic acid, 22-methyl-5,9-octacosadienoic acid
-
Raederstorff, D.; Shu, A.Y.L.; Thompson, J.E.; Djerassi, C. Biosynthetic studies of marine lipids. 11. Synthesis, biosynthesis, and absolute configuration of the internally branched demospongic acid, 22-methyl-5,9- octacosadienoic acid. J. Org. Chem. 1987, 52, 2337-2346.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 2337-2346
-
-
Raederstorff, D.1
Shu, A.Y.L.2
Thompson, J.E.3
Djerassi, C.4
-
45
-
-
0000928356
-
Bengamides are novel marine natural products with broad spectrum antitumor activity
-
Kinder, F.R.; Bair, K.W.; Bontempo, J.; Crews, P.; Czuchta, A.M.; Nemzek, R.; Thale, Z.; Vattay, A.; Versace, R.W.; Weltchek, S.; Wood, A.; Zabludoff, S.D.; Phillips, P.E. Bengamides are novel marine natural products with broad spectrum antitumor activity. Proc. Am. Assoc. Cancer Res. 2000, 41, 600.
-
(2000)
Proc. Am. Assoc. Cancer Res.
, vol.41
, pp. 600
-
-
Kinder, F.R.1
Bair, K.W.2
Bontempo, J.3
Crews, P.4
Czuchta, A.M.5
Nemzek, R.6
Thale, Z.7
Vattay, A.8
Versace, R.W.9
Weltchek, S.10
Wood, A.11
Zabludoff, S.D.12
Phillips, P.E.13
-
46
-
-
0035950061
-
Synthesis and antitumor activity of ester-modified analogues of bengamide B
-
Kinder, F.R., Jr.; Versace, R.W.; Bair, K.W.; Bontempo, J.M.; Cesarz, D.; Chen, S.; Crews, P.; Czuchta, A.M.; Jagoe, C.T.; Mou, Y.; et al. Synthesis and antitumor activity of ester-modified analogues of bengamide B. J. Med. Chem. 2001, 44, 3692-3699.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3692-3699
-
-
Kinder Jr.1
, F.R.2
Versace, R.W.3
Bair, K.W.4
Bontempo, J.M.5
Cesarz, D.6
Chen, S.7
Crews, P.8
Czuchta, A.M.9
Jagoe, C.T.10
Mou, Y.11
-
47
-
-
0001801683
-
Bengamide E arrests cells at the G1/S restriction point and within the G2/M phase of the cell cycle
-
Phillips, P.E.; Bair, K.W.; Bontempo, J.; Crews, P.; Czuchta, M.; Kinder, F.R.; Versace, R.W.; Wang, B.; Wang, J.; Wood, A.; et al. Bengamide E arrests cells at the G1/S restriction point and within the G2/M phase of the cell cycle. Proc. Am. Assoc. Cancer Res. 2000, 41, 59.
-
(2000)
Proc. Am. Assoc. Cancer Res.
, vol.41
, pp. 59
-
-
Phillips, P.E.1
Bair, K.W.2
Bontempo, J.3
Crews, P.4
Czuchta, M.5
Kinder, F.R.6
Versace, R.W.7
Wang, B.8
Wang, J.9
Wood, A.10
-
48
-
-
9144222006
-
Proteomics-based target identification: Bengamides as a new class of methionine aminopeptidase inhibitors
-
Towbin, H.; Bair, K.W.; DeCaprio, J.A.; Eck, M.J.; Kim, S.; Kinder, F.R.; Morollo, A.; Mueller, D.R.; Schindler, P.; Song, H.K.; et al. Proteomics-based target identification: Bengamides as a new class of methionine aminopeptidase inhibitors. J. Biol. Chem. 2003, 278, 52964-52971.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 52964-52971
-
-
Towbin, H.1
Bair, K.W.2
DeCaprio, J.A.3
Eck, M.J.4
Kim, S.5
Kinder, F.R.6
Morollo, A.7
Mueller, D.R.8
Schindler, P.9
Song, H.K.10
-
49
-
-
0347365752
-
An Expedient Synthesis of LAF389, a Bengamide B Analogue
-
DOI 10.1021/op0341162
-
Xu, D.D.; Waykole, L.; Calienni, J.V.; Ciszewski, L.; Lee, G.T.; Liu, W.; Szewczyk, J.; Vargas, K.; Prasad, K.; Repič, O.; et al. An expedient synthesis of LAF389, a bengamide B analogue. Org. Process. Res. Dev. 2003, 7, 856-865. (Pubitemid 37543804)
-
(2003)
Organic Process Research and Development
, vol.7
, Issue.6
, pp. 856-865
-
-
Xu, D.D.1
Waykole, L.2
Calienni, J.V.3
Ciszewski, L.4
Lee, G.T.5
Liu, W.6
Szewczyk, J.7
Vargas, K.8
Prasad, K.9
Repic, O.10
Blacklock, T.J.11
-
50
-
-
0035473486
-
14-3-3 Proteins; bringing new definitions to scaffolding
-
DOI 10.1038/sj.onc.1204777
-
Tzivion, G.; Shen, Y.H.; Zhu, J. 14-3-3 proteins; bringing new definitions to scaffolding. Oncogene 2001, 20, 6331-6338. (Pubitemid 32977842)
-
(2001)
Oncogene
, vol.20
, Issue.44 REV. ISS. 5
, pp. 6331-6338
-
-
Tzivion, G.1
Shen, Y.H.2
Zhu, J.3
-
51
-
-
13044300888
-
Molecular recognition of angiogenesis inhibitors fumagillin and ovalicin by methionine aminopeptidase 2
-
DOI 10.1073/pnas.95.26.15183
-
Griffith, E.C.; Su, Z.; Niwayama, S.; Ramsay, C.A.; Chang, Y.H.; Liu, J.O. Molecular recognition of angiogenesis inhibitors fumagillin and ovalicin by methionine aminopeptidase 2. Proc. Natl. Acad. Sci. USA 1998, 95, 15183-15188. (Pubitemid 29018673)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.26
, pp. 15183-15188
-
-
Griffith, E.C.1
Zhuang, S.U.2
Niwayama, S.3
Ramsay, C.A.4
Chang, Y.-H.5
Liu, J.O.6
-
52
-
-
0031171961
-
Methionine aminopeptidase (type 2) is the common target for angiogenesis inhibitors AGM-1470 and ovalicin
-
Griffith, E.C.; Su, Z.; Turk, B.E.; Chen, S.; Chang, Y.H.; Wu, Z.; Biemann, K.; Liu, J.O. Methionine aminopeptidase (type 2) is the common target for angiogenesis inhibitors AGM-1470 and ovalicin. Chem. Biol. 1997, 4, 461-471. (Pubitemid 27288711)
-
(1997)
Chemistry and Biology
, vol.4
, Issue.6
, pp. 461-471
-
-
Griffith, E.C.1
Su, Z.2
Turk, B.E.3
Chen, S.4
Chang, Y.-H.5
Wu, Z.6
Biemann, K.7
Liu, J.O.8
-
53
-
-
34447547502
-
Regulation of c-Src Nonreceptor Tyrosine Kinase Activity by Bengamide A through Inhibition of Methionine Aminopeptidases
-
DOI 10.1016/j.chembiol.2007.05.010, PII S1074552107001792
-
Hu, X.; Dang, Y.; Tenney, K.; Crews, P.; Tsai, C.W.; Sixt, K.M.; Cole, P.A.; Liu, J.O. Regulation of c-Src nonreceptor tyrosine kinase activity by bengamide A through inhibition of methionine aminopeptidases. Chem. Biol. 2007, 14, 764-774. (Pubitemid 47081418)
-
(2007)
Chemistry and Biology
, vol.14
, Issue.7
, pp. 764-774
-
-
Hu, X.1
Dang, Y.2
Tenney, K.3
Crews, P.4
Tsai, C.W.5
Sixt, K.M.6
Cole, P.A.7
Liu, J.O.8
-
54
-
-
65249142193
-
A selective account of effective paradigms and significant outcomes in the discovery of inspirational marine natural products
-
Sashidhara, K.V.; White, K.N.; Crews, P. A selective account of effective paradigms and significant outcomes in the discovery of inspirational marine natural products. J. Nat. Prod. 2009, 72, 588-603.
-
(2009)
J. Nat. Prod.
, vol.72
, pp. 588-603
-
-
Sashidhara, K.V.1
White, K.N.2
Crews, P.3
-
55
-
-
0034615568
-
Structure and function of the methionine aminopeptidases
-
DOI 10.1016/S0167-4838(99)00271-X, PII S016748389900271X
-
Lowther, W.T.; Matthews, B.W. Structure and function of the methionine aminopeptidases. Biochim. Biophys. Acta 2000, 1477, 157-167. (Pubitemid 30119899)
-
(2000)
Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
, vol.1477
, Issue.1-2
, pp. 157-167
-
-
Lowther, W.T.1
Matthews, B.W.2
-
56
-
-
3042807051
-
Protein N-terminal methionine excision
-
Giglione, C.; Boularot, A.; Meinnel, T. Protein N-terminal methionine excision. Cell. Mol. Life Sci. 2004, 61, 1455-1474. (Pubitemid 38858352)
-
(2004)
Cellular and Molecular Life Sciences
, vol.61
, Issue.12
, pp. 1455-1474
-
-
Giglione, C.1
Boularot, A.2
Meinnel, T.3
-
57
-
-
0023135722
-
Processing of the initiation methionine from proteins: Properties of the Escherichia coli methionine aminopeptidase and its gene structure
-
Ben-Bassat, A.; Bauer, K.; Chang, S.Y.; Myambo, K.; Boosman, A. Processing of the initiation methionine from proteins: Properties of the Escherichia coli methionine aminopeptidase and its gene structure. J. Bacteriol. 1987, 169, 751-757.
-
(1987)
J. Bacteriol.
, vol.169
, pp. 751-757
-
-
Ben-Bassat, A.1
Bauer, K.2
Chang, S.Y.3
Myambo, K.4
Boosman, A.5
-
58
-
-
0030941458
-
p53, the cellular gatekeeper for growth and division
-
DOI 10.1016/S0092-8674(00)81871-1
-
Levine, A.J. p53, the cellular gatekeeper for growth and division. Cell 1997, 88, 323-331. (Pubitemid 27131374)
-
(1997)
Cell
, vol.88
, Issue.3
, pp. 323-331
-
-
Levine, A.J.1
-
59
-
-
0028198617
-
Sequence and structure comparison suggest that methionine aminopeptidase, prolidase, aminopeptidase P, and creatinase share a common fold
-
Bazan, J.F.; Weaver, L.H.; Roderick, S.L.; Huber, R.; Matthews, B.W. Sequence and structure comparison suggest that methionine aminopeptidase, prolidase, aminopeptidase P, and creatinase share a common fold. Proc. Natl. Acad. Sci. USA 1994, 91, 2473-2477. (Pubitemid 24139369)
-
(1994)
Proceedings of the National Academy of Sciences of the United States of America
, vol.91
, Issue.7
, pp. 2473-2477
-
-
Bazan, J.F.1
Weaver, L.H.2
Roderick, S.L.3
Huber, R.4
Matthews, B.W.5
-
60
-
-
0029099158
-
Eukaryotic methionyl aminopeptidases: Two classes of cobalt-dependent enzymes
-
Arfin, S.M.; Kendall, R.L.; Hall, L.; Weaver, L.H.; Stewart, A.E.; Matthews, B.W.; Bradshaw, R.A. Eukaryotic methionyl aminopeptidases: Two classes of cobalt-dependent enzymes. Proc. Natl. Acad. Sci. USA 1995, 92, 7714-7718.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 7714-7718
-
-
Arfin, S.M.1
Kendall, R.L.2
Hall, L.3
Weaver, L.H.4
Stewart, A.E.5
Matthews, B.W.6
Bradshaw, R.A.7
-
61
-
-
0032127904
-
N-terminal processing: The methionine aminopeptidase and N-acetyl transferase families
-
Bradshaw, R.A.; Brickey, W.W.; Walder, K.W. N-terminal processing: The methionine aminopeptidase and N-acetyl transferase families. Trends Biochem. Sci. 1998, 23, 263-267.
-
(1998)
Trends Biochem. Sci.
, vol.23
, pp. 263-267
-
-
Bradshaw, R.A.1
Brickey, W.W.2
Walder, K.W.3
-
62
-
-
27744565323
-
Structural basis for the functional differences between type I and type II human methionine aminopeptidases
-
DOI 10.1021/bi051691k
-
Addlagatta, A.; Hu, X.; Liu, J.O.; Matthews, B.W. Structural basis for the functional differences between type I and type II human methionine aminopeptidases. Biochemistry 2005, 44, 14741-14749. (Pubitemid 41612254)
-
(2005)
Biochemistry
, vol.44
, Issue.45
, pp. 14741-14749
-
-
Addlagatta, A.1
Hu, X.2
Liu, J.O.3
Matthews, B.W.4
-
63
-
-
0032515029
-
Structure of human methionine aminopeptidase-2 complexed with fumagillin
-
Liu, S. Structure of human methionine aminopeptidase-2 complexed with fumagillin. Science 1998, 282, 1324-1327. (Pubitemid 28524496)
-
(1998)
Science
, vol.282
, Issue.5392
, pp. 1324-1327
-
-
Liu, S.1
Widom, J.2
Kemp, C.W.3
Crews, C.M.4
Clardy, J.5
-
64
-
-
0025204095
-
Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth
-
Ingber, D.; Fujita, T.; Kishimoto, S.; Sudo, K.; Kanamaru, T.; Brem, H.; Folkman, J. Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature 1990, 348, 555-557. (Pubitemid 120015110)
-
(1990)
Nature
, vol.348
, Issue.6301
, pp. 555-557
-
-
Ingber, D.1
Fujita, T.2
Kishimoto, S.3
Sudo, K.4
Kanamaru, T.5
Brem, H.6
Folkman, J.7
-
65
-
-
16644386079
-
Role of aminopeptidase in angiogenesis
-
DOI 10.1248/bpb.27.772
-
Sato, Y. Aminopeptidases in health and disease: Role of aminopeptidase in angiogenesis. Biol. Pharm. Bull. 2004, 27, 772-776. (Pubitemid 41701786)
-
(2004)
Biological and Pharmaceutical Bulletin
, vol.27
, Issue.6
, pp. 772-776
-
-
Sato, Y.1
-
66
-
-
0033564306
-
Escherichia coli methionine aminopeptidase: Implications of crystallographic analyses of the native, mutant and inhibited enzymes for the mechanism of catalysis
-
Lowther, W.T.; Orville, A.M.; Madded, D.T.; Lim, S.; Rich, D.H.; Matthews, B.W. Escherichia coli methionine aminopeptidase: Implications of crystallographic analyses of the native, mutant and inhibited enzymes for the mechanism of catalysis. Biochemistry 1999, 38, 7678-7688.
-
(1999)
Biochemistry
, vol.38
, pp. 7678-7688
-
-
Lowther, W.T.1
Orville, A.M.2
Madded, D.T.3
Lim, S.4
Rich, D.H.5
Matthews, B.W.6
-
67
-
-
84866863979
-
Structural analysis of bengamide derivatives as inhibitors of methionine aminopeptidases
-
Xu, W.; Lu, J.P.; Ye, Q.Z. Structural analysis of bengamide derivatives as inhibitors of methionine aminopeptidases. J. Med. Chem. 2012, 55, 8021-8027.
-
(2012)
J. Med. Chem.
, vol.55
, pp. 8021-8027
-
-
Xu, W.1
Lu, J.P.2
Ye, Q.Z.3
-
68
-
-
33845310513
-
Elucidation of the function of type 1 human methionine aminopeptides during cell cycle progression
-
DOI 10.1073/pnas.0608389103
-
Hu, X.; Addlagatta, A.; Lu, J.; Matthews, B.W.; Liu, J.O. Elucidation of the function of type 1 human methionine aminopeptidase during cell cycle progression. Proc. Natl. Acad. Sci. USA 2006, 103, 18148-18153. (Pubitemid 44871627)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.48
, pp. 18148-18153
-
-
Hu, X.1
Addlagatta, A.2
Lu, J.3
Matthews, B.W.4
Liu, J.O.5
-
69
-
-
0038792294
-
Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae
-
Luo, Q.L.; Li, J.Y.; Liu, Z.Y.; Chen, L.L.; Li, J.; Qian, Z.; Shen, Q.; Li, Y.; Lushington, G.H.; Ye, Q.Z.; et al. Discovery and structural modification of inhibitors of methionine aminopeptidases from Escherichia coli and Saccharomyces cerevisiae. J. Med. Chem. 2003, 46, 2631-2640.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2631-2640
-
-
Luo, Q.L.1
Li, J.Y.2
Liu, Z.Y.3
Chen, L.L.4
Li, J.5
Qian, Z.6
Shen, Q.7
Li, Y.8
Lushington, G.H.9
Ye, Q.Z.10
-
70
-
-
2942750310
-
Characterization of full length and truncated type I human methionine aminopeptidases expressed from Escherichia coli
-
Li, J.Y.; Chen, L.L.; Cui, Y.M.; Luo, Q.L.; Gu, M.; Nan, F.J.; Ye, Q.Z. Characterization of full length and truncated type I human methionine aminopeptidases expressed from Escherichia coli. Biochemistry 2004, 43, 7892-7898.
-
(2004)
Biochemistry
, vol.43
, pp. 7892-7898
-
-
Li, J.Y.1
Chen, L.L.2
Cui, Y.M.3
Luo, Q.L.4
Gu, M.5
Nan, F.J.6
Ye, Q.Z.7
-
71
-
-
0034693877
-
Role of Src expression and activation in human cancer
-
Irby, R.B.; Yeatman, T.J. Role of Src expression and activation in human cancer. Oncogene 2000, 19, 5636-5642.
-
(2000)
Oncogene
, vol.19
, pp. 5636-5642
-
-
Irby, R.B.1
Yeatman, T.J.2
-
72
-
-
2342640861
-
Depletion of Methionine Aminopeptidase 2 Does Not Alter Cell Response to Fumagillin or Bengamides
-
DOI 10.1158/0008-5472.CAN-04-0019
-
Kim, S. Depletion of methionine aminopeptidase 2 does not alter cell response to fumagillin or bengamides. Cancer Res. 2004, 64, 2984-2987. (Pubitemid 38581392)
-
(2004)
Cancer Research
, vol.64
, Issue.9
, pp. 2984-2987
-
-
Kim, S.1
LaMontagne, K.2
Sabio, M.3
Sharma, S.4
Versace, R.W.5
Yusuff, N.6
Phillips, P.E.7
-
73
-
-
22244488279
-
Methionine aminopeptidases type I and type II are essential to control cell proliferation
-
DOI 10.1002/jcb.20493
-
Bernier, S.G.; Taghizadeh, N.; Thompson, C.D.; Westlin, W.F.; Hannig, G. Methionine aminopeptidases type I and type II are essential to control cell proliferation. J. Cell. Biochem. 2005, 95, 1191-1203. (Pubitemid 41420126)
-
(2005)
Journal of Cellular Biochemistry
, vol.95
, Issue.6
, pp. 1191-1203
-
-
Bernier, S.G.1
Taghizadeh, N.2
Thompson, C.D.3
Westlin, W.F.4
Hannig, G.5
-
74
-
-
0025793674
-
An enantiospecific approach towards the C10 side-chain of bengamides
-
Gurjar, M.K.; Srinivas, N.R. An enantiospecific approach towards the C10 side-chain of bengamides. Tetrahedron Lett. 1991, 32, 3409-3412.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 3409-3412
-
-
Gurjar, M.K.1
Srinivas, N.R.2
-
75
-
-
0035937275
-
Total synthesis of bengamides B and E
-
Kinder, F.R., Jr.; Wattanasin, S.; Versace, R.W.; Bair, K.W.; Bontempo, J.; Green, M.A.; Lu, Y.J.; Marepalli, H.R.; Phillips, P.E.; Roche, D.; et al. Total synthesis of bengamides B and E. J. Org. Chem. 2001, 66, 2118-2122.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 2118-2122
-
-
Kinder Jr.1
, F.R.2
Wattanasin, S.3
Versace, R.W.4
Bair, K.W.5
Bontempo, J.6
Green, M.A.7
Lu, Y.J.8
Marepalli, H.R.9
Phillips, P.E.10
Roche, D.11
-
76
-
-
0026742940
-
An enantioselective synthesis of bengamide E
-
Kishimoto, H.; Ohrui, H.; Meguro, H. An enantioselective synthesis of bengamide E. J. Org. Chem. 1992, 57, 5042-5044.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5042-5044
-
-
Kishimoto, H.1
Ohrui, H.2
Meguro, H.3
-
77
-
-
0027132423
-
Stereoselective total synthesis of bengamide E from glyceraldehyde acetonide and a nonracemic γ-alkoxy allylic stannane
-
DOI 10.1021/jo00075a017
-
Marshall, J.A.; Luke, G.P. Stereoselective total synthesis of bengamide E from glyceraldehyde acetonide and a nonracemic γ-alkoxy allylic stannane. J. Org. Chem. 1993, 58, 6229-6234. (Pubitemid 24010194)
-
(1993)
Journal of Organic Chemistry
, vol.58
, Issue.23
, pp. 6229-6234
-
-
Marshall, J.A.1
Luke, G.P.2
-
78
-
-
4644337745
-
Highly stereocontrolled total synthesis of (+)-bengamide E
-
doi:10.1039/P19950002849
-
Mukai, C.; Moharram, S.M.; Kataoka, O.; Hanaoka, M. Highly stereocontrolled total synthesis of (+)-bengamide E. J. Chem. Soc. Perkin Trans. I 1995, 2849-2854; doi:10.1039/P19950002849.
-
(1995)
J. Chem. Soc. Perkin Trans. I
, pp. 2849-2854
-
-
Mukai, C.1
Moharram, S.M.2
Kataoka, O.3
Hanaoka, M.4
-
79
-
-
0028146803
-
A cobalt-complexed propynal in organic synthesis: A highly stereoselective total syntheis of bengamide E
-
Mukai, C.; Kataoka, O.; Hanaoka, M. A cobalt-complexed propynal in organic synthesis: A highly stereoselective total syntheis of bengamide E. Tetrahedron Lett. 1994, 35, 6899-6902.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 6899-6902
-
-
Mukai, C.1
Kataoka, O.2
Hanaoka, M.3
-
80
-
-
0029084214
-
An efficient method for the optical resolution of 3-hydroxy-2- substituted-4-alkylnoates: A highly stereoselective total syntheis of (+)-bengamide E
-
Mukai, C.; Kataoka, O.; Hanaoka, M. An efficient method for the optical resolution of 3-hydroxy-2-substituted-4-alkylnoates: A highly stereoselective total syntheis of (+)-bengamide E. J. Org. Chem. 1995, 60, 5910-5918.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 5910-5918
-
-
Mukai, C.1
Kataoka, O.2
Hanaoka, M.3
-
81
-
-
0000238264
-
Stereoselective conversion of L-quebrachitol into a novel hydroxylated caprolactam: Total synthesis of bengamide B
-
Chida, N.; Tobe, T.; Murai, K.; Yamazaki, K.; Ogawa, S. Stereoselective conversion of L-quebrachitol into a novel hydroxylated caprolactam: total synthesis of bengamide B. Heterocycles 1994, 38, 2383-2388.
-
(1994)
Heterocycles
, vol.38
, pp. 2383-2388
-
-
Chida, N.1
Tobe, T.2
Murai, K.3
Yamazaki, K.4
Ogawa, S.5
-
82
-
-
0036941570
-
Synthetic approaches toward the bengamide family of antitumor marine natural products. A review
-
Kinder, F.R., Jr. Synthetic approaches toward the bengamide family of antitumor marine natural products. A review. Org. Prep. Proc. Int. 2002, 34, 559-583.
-
(2002)
Org. Prep. Proc. Int.
, vol.34
, pp. 559-583
-
-
Kinder Jr., F.R.1
-
83
-
-
0035812744
-
A chemoenzymatic total synthesis of ent-bengamide E
-
DOI 10.1021/jo0159486
-
Banwell, M.G.; McRae, K.J. A chemoenzymatic total synthesis of ent-bengamide E. J. Org. Chem. 2001, 66, 6768-6774. (Pubitemid 32946598)
-
(2001)
Journal of Organic Chemistry
, vol.66
, Issue.20
, pp. 6768-6774
-
-
Banwell, M.G.1
McRae, K.J.2
-
84
-
-
0037127506
-
Total synthesis of bengamide E
-
DOI 10.1016/S0040-4039(02)00022-9, PII S0040403902000229
-
Liu, W.; Szewczyk, J.M.; Waykole, L.; Repic, O.; Blacklock, T.J. Total synthesis of bengamide E. Tetrahedron Lett. 2002, 43, 1373-1375. (Pubitemid 34142414)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.8
, pp. 1373-1375
-
-
Liu, W.1
Szewczyk, J.M.2
Waykole, L.3
Repic, O.4
Blacklock, T.J.5
-
85
-
-
0000735939
-
Diastereoselective synthesis of anti and syn α,β-dihydroxy thioesters by titanium enolate aldol condensation
-
Annunziata, R.; Cinquini, M.; Cozzi, F.; Borgia, A.L. Diastereoselective synthesis of anti and syn α,β-dihydroxy thioesters by titanium enolate aldol condensation. J. Org. Chem. 1992, 57, 6339-6342.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 6339-6342
-
-
Annunziata, R.1
Cinquini, M.2
Cozzi, F.3
Borgia, A.L.4
-
86
-
-
0037071927
-
A practical enantioselective total synthesis of the bengamides B, E, and Z
-
Boeckman, R.K., Jr.; Clark, T.J.; Shook, B.C. A practical enantioselective total synthesis of the bengamides B, E, and Z. Org. Lett. 2002, 4, 2109-2112.
-
(2002)
Org. Lett.
, vol.4
, pp. 2109-2112
-
-
Boeckman Jr.1
, R.K.2
Clark, T.J.3
Shook, B.C.4
-
87
-
-
0036959660
-
The development of a convergent and efficient enantioselective synthesis of the bengamides via a common polyol intermediate
-
DOI 10.1002/hlca.200290026
-
Boeckman, R.K., Jr.; Clark, T.J.; Shook, B.C. The development of a convergent and efficient enantioselective synthesis of the bengamides via a common polyol intermediate. Helv. Chim. Acta 2002, 85, 4532-4560. (Pubitemid 36119162)
-
(2002)
Helvetica Chimica Acta
, vol.85
, Issue.12
, pp. 4532-4560
-
-
Boeckman Jr., R.K.1
Clark, T.J.2
Shook, B.C.3
-
88
-
-
12344280267
-
A diversity-oriented synthetic approach to bengamides
-
DOI 10.1016/j.tetlet.2004.12.096, PII S0040403904027996
-
Sarabia, F.; Sánchez-Ruiz, A. A diversity-oriented synthetic approach to bengamides. Tetrahedron Lett. 2005, 46, 1131-1135. (Pubitemid 40138897)
-
(2005)
Tetrahedron Letters
, vol.46
, Issue.7
, pp. 1131-1135
-
-
Sarabia, F.1
Sanchez-Ruiz, A.2
-
89
-
-
27744490356
-
Total synthesis of bengamide E and analogues by modification at C-2 and at terminal olefinic positions
-
DOI 10.1021/jo0516032
-
Sarabia, F.; Sánchez-Ruiz, A. Total synthesis of bengamide E and analogues by modification at C-2 and at terminal olefinic positions. J. Org. Chem. 2005, 70, 9514-9520. (Pubitemid 41611707)
-
(2005)
Journal of Organic Chemistry
, vol.70
, Issue.23
, pp. 9514-9520
-
-
Sarabia, F.1
Sanchez-Ruiz, A.2
-
90
-
-
84869106890
-
A highly stereoselective synthesis of glycidic amides based on a new class of chiral sulfonium salts: Applications in asymmetric synthesis
-
Sarabia, F.; Vivar-García, C.; García-Castro, M.; García-Ruiz, C.; Martín-Gálvez, F.; Sánchez-Ruiz, A.; Chammaa, S. A highly stereoselective synthesis of glycidic amides based on a new class of chiral sulfonium salts: Applications in asymmetric synthesis. Chem. Eur. J. 2012, 18, 15190-15201.
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 15190-15201
-
-
Sarabia, F.1
Vivar-García, C.2
García-Castro, M.3
García-Ruiz, C.4
Martín-Gálvez, F.5
Sánchez-Ruiz, A.6
Chammaa, S.7
-
91
-
-
0141674890
-
The C2 selective nucleophilic substitution reactions of 2,3-epoxy alcohols mediated by trialkyl borates: The first endo-mode epoxide-opening reaction through an intramolecular metal chelate
-
DOI 10.1021/ol034455f
-
Sasaki, M.; Tanino, K.; Hirai, A.; Miyashita, M. The C2 selective nucleophilic substitution reactions of 2,3-epoxy alcohols mediated by trialkyl borates: The first endo-mode epoxide-opening reaction through an intramolecular metal chelate. Org. Lett. 2003, 5, 1789-1791. (Pubitemid 37162030)
-
(2003)
Organic Letters
, vol.5
, Issue.10
, pp. 1789-1791
-
-
Sasaki, M.1
Tanino, K.2
Hirai, A.3
Miyashita, M.4
-
92
-
-
84877032456
-
Concise synthesis and antitumor activity of bengamide E and its analogs
-
Zhang, W.; Liang, Q.; Li, H.; Meng, X.; Li, Z. Concise synthesis and antitumor activity of bengamide E and its analogs. Tetrahedron 2013, 69, 664-672.
-
(2013)
Tetrahedron
, vol.69
, pp. 664-672
-
-
Zhang, W.1
Liang, Q.2
Li, H.3
Meng, X.4
Li, Z.5
-
93
-
-
84873817012
-
Enantiospecific total synthesis of (-)-bengamide E
-
Metri, P.K.; Schiess, R.; Prasad, K.R. Enantiospecific total synthesis of (-)-bengamide E. Chem. Asian J. 2013, 8, 488-493.
-
(2013)
Chem. Asian J.
, vol.8
, pp. 488-493
-
-
Metri, P.K.1
Schiess, R.2
Prasad, K.R.3
-
94
-
-
0000772702
-
Iterative, stereoselective homologation of chiral polyalkoxy aldehydes employing 2-(trimethylsilyl)thiazole as a formyl anion equivalent. The thiazole route to higher carbohydrates
-
Dondoni, A.; Fantin, G.; Fogagnolo, M.; Medici, A.; Pedrini, P. Iterative, stereoselective homologation of chiral polyalkoxy aldehydes employing 2-(trimethylsilyl)thiazole as a formyl anion equivalent. The thiazole route to higher carbohydrates. J. Org. Chem. 1989, 54, 693-702.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 693-702
-
-
Dondoni, A.1
Fantin, G.2
Fogagnolo, M.3
Medici, A.4
Pedrini, P.5
-
95
-
-
41649100723
-
Stereoselective total synthesis of (+)-cardiobutanolide
-
DOI 10.1021/jo7025614
-
Prasad, K.R.; Gholap, S.L. Stereoselective total synthesis of (+)-cardiobutanolide. J. Org. Chem. 2008, 73, 2916-2919. (Pubitemid 351483010)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.7
, pp. 2916-2919
-
-
Prasad, K.R.1
Gholap, S.L.2
-
96
-
-
0002227833
-
A convenient Synthesis of ethylidine iodide
-
Friedrich, E.C.; Falling, S.N.; Lyons, D.E. A convenient Synthesis of ethylidine iodide. Synth. Commun. 1975, 5, 33-36.
-
(1975)
Synth. Commun.
, vol.5
, pp. 33-36
-
-
Friedrich, E.C.1
Falling, S.N.2
Lyons, D.E.3
-
97
-
-
33845715488
-
A phase I and pharmacokinetic study of LAF389 administered to patients with advanced cancer
-
DOI 10.1097/CAD.0b013e328010ef5b, PII 0000181320070200000013
-
Dumez, H.; Gall, H.; Capdeville, R.; Dutreix, C.; van Oosterom, A.T.; Giaccone, G. A phase I and pharmacokinetic study of LAF389 administered to patients with advanced cancer. Anti-Cancer Drugs 2007, 18, 219-225. (Pubitemid 44967432)
-
(2007)
Anti-Cancer Drugs
, vol.18
, Issue.2
, pp. 219-225
-
-
Dumez, H.1
Gall, H.2
Capdeville, R.3
Dutreix, C.4
Van Oosterom, A.T.5
Giaccone, G.6
-
98
-
-
33646472886
-
Facile synthesis of versatile functionalized amino caprolactams using RCM reactions of α-amino acrylamide
-
Liu, G.; Tai, W.-Y.; Li, Y.-L.; Nan, F.-J. Facile synthesis of versatile functionalized amino caprolactams using RCM reactions of α-amino acrylamide. Tetrahedron Lett. 2006, 47, 3295-3298.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3295-3298
-
-
Liu, G.1
Tai, W.-Y.2
Li, Y.-L.3
Nan, F.-J.4
-
99
-
-
47249146133
-
Design, synthesis, and biological evaluation of caprolactam-modified bengamide analogues
-
Liu, G.; Ma, Y.M.; Tai, W.Y.; Xie, C.M.; Li, Y.L.; Li, J.; Nan, F.J. Design, synthesis, and biological evaluation of caprolactam-modified bengamide analogues. ChemMedChem 2008, 3, 74-78.
-
(2008)
ChemMedChem
, vol.3
, pp. 74-78
-
-
Liu, G.1
Ma, Y.M.2
Tai, W.Y.3
Xie, C.M.4
Li, Y.L.5
Li, J.6
Nan, F.J.7
-
100
-
-
80052108794
-
Design, synthesis, and biological evaluation of ring-opened bengamide analogues
-
Tai, W.Y.; Zhang, R.T.; Ma, Y.M.; Gu, M.; Liu, G.; Li, J.; Nan, F.J. Design, synthesis, and biological evaluation of ring-opened bengamide analogues. ChemMedChem 2011, 6, 1555-1558.
-
(2011)
ChemMedChem
, vol.6
, pp. 1555-1558
-
-
Tai, W.Y.1
Zhang, R.T.2
Ma, Y.M.3
Gu, M.4
Liu, G.5
Li, J.6
Nan, F.J.7
-
101
-
-
79957587056
-
Inhibition of Mycobacterium tuberculosis methionine aminopeptidases by bengamide derivatives
-
Lu, J.P.; Yuan, X.H.; Yuan, H.; Wang, W.L.; Wan, B.; Franzblau, S.G.; Ye, Q.Z. Inhibition of Mycobacterium tuberculosis methionine aminopeptidases by bengamide derivatives. ChemMedChem 2011, 6, 1041-1048.
-
(2011)
ChemMedChem
, vol.6
, pp. 1041-1048
-
-
Lu, J.P.1
Yuan, X.H.2
Yuan, H.3
Wang, W.L.4
Wan, B.5
Franzblau, S.G.6
Ye, Q.Z.7
-
102
-
-
79952986829
-
Synthesis of (3S,4R)-bengamide E
-
Liu, Q.J.; Li, H.; Chen, S.P.; Zhou, G.C. Synthesis of (3S,4R)-bengamide E. Chin. Chem. Lett. 2011, 22, 505-507.
-
(2011)
Chin. Chem. Lett.
, vol.22
, pp. 505-507
-
-
Liu, Q.J.1
Li, H.2
Chen, S.P.3
Zhou, G.C.4
-
103
-
-
84879283013
-
Epi -, epoxy-, and C2-modified bengamides: Synthesis and biological evaluation
-
Sarabia, F.; Martín-Gálvez, F.; García-Ruiz, C.; Sánchez-Ruiz, A.; Vivar-García, C. Epi -, epoxy-, and C2-modified bengamides: synthesis and biological evaluation. J. Org. Chem. 2013, 78, 5239-5253.
-
(2013)
J. Org. Chem.
, vol.78
, pp. 5239-5253
-
-
Sarabia, F.1
Martín-Gálvez, F.2
García-Ruiz, C.3
Sánchez-Ruiz, A.4
Vivar-García, C.5
-
104
-
-
84877025501
-
An array of bengamide E analogues modified at the terminal olefinic position: Synthesis and antitumor properties
-
Martín-Gálvez, F.; García-Ruiz, C.; Sánchez-Ruiz, A.; Valeriote, F.A.; Sarabia, F. An array of bengamide E analogues modified at the terminal olefinic position: Synthesis and antitumor properties. ChemMedChem 2013, 8, 819-831.
-
(2013)
ChemMedChem
, vol.8
, pp. 819-831
-
-
Martín-Gálvez, F.1
García-Ruiz, C.2
Sánchez-Ruiz, A.3
Valeriote, F.A.4
Sarabia, F.5
-
105
-
-
22744442306
-
Palladium-catalyzed cross-coupling reactions in total synthesis
-
DOI 10.1002/anie.200500368
-
Nicolaou, K.C.; Bulger, P.G.; Sarlah, D. Palladium-catalyzed cross-coupling reactions in total synthesis. Angew. Chem. Int. Ed. 2005, 44, 4442-4489. (Pubitemid 41026385)
-
(2005)
Angewandte Chemie - International Edition
, vol.44
, Issue.29
, pp. 4442-4489
-
-
Nicolaou, K.C.1
Bulger, P.G.2
Sarlah, D.3
-
106
-
-
9644285669
-
A convenient synthesis of acetylenes: Catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
-
Sonogashira, K.; Tohda, Y.; Hagihara, N. A convenient synthesis of acetylenes: Catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines. Tetrahedron Lett. 1975, 50, 4467-4470.
-
(1975)
Tetrahedron Lett.
, vol.50
, pp. 4467-4470
-
-
Sonogashira, K.1
Tohda, Y.2
Hagihara, N.3
-
107
-
-
0242490677
-
Clean Inversion of Configuration in the Pd-Catalyzed Cross-Coupling of 2-Bromo-1,3-dienes
-
DOI 10.1021/ja0304392
-
Zeng, X.; Hu, Q.; Qian, M.; Negishi, E. Clean inversion of configuration in the Pd-catalyzed cross-coupling of 2-bromo-1,3-dienes. J. Am. Chem. Soc. 2003, 125, 13636-13637. (Pubitemid 37386018)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.45
, pp. 13636-13637
-
-
Zeng, X.1
Hu, Q.2
Qian, M.3
Negishi, E.-I.4
-
108
-
-
2342552606
-
-
Department of Chemistry, University of Rochester: Rochester, NY, USA
-
Clark, T.J. Part I. Total Synthesis of Bengamide Z: Part II. Studies Toward Asymmetric Acylation of α-Oxygenated Imides; Department of Chemistry, University of Rochester: Rochester, NY, USA, 2001; p. 225.
-
(2001)
Part I. Total Synthesis of Bengamide Z: Part II. Studies Toward Asymmetric Acylation of α-Oxygenated Imides
, pp. 225
-
-
Clark, T.J.1
-
109
-
-
0027761764
-
New structures and bioactivity patterns of bengazole alkaloids from a choristid marine sponge
-
Rodríguez, J.; Nieto, R.M.; Crews, P. New structures and bioactivity patterns of bengazole alkaloids from a choristid marine sponge. J. Nat. Prod. 1993, 56, 2034-2040. (Pubitemid 24034008)
-
(1993)
Journal of Natural Products
, vol.56
, Issue.12
, pp. 2034-2040
-
-
Rodriguez, J.1
Nieto, R.M.2
Crews, P.3
-
110
-
-
42249086977
-
Antineoplastic agents. 536. New sources of naturally occurring cancer cell growth inhibitors from marine organisms, terrestrial plants, and microorganisms
-
1a
-
Pettit, G.R.; Hogan, F.; Xu, J.P.; Tan, R.; Nogawa, T.; Cichacz, Z.; Pettit, R.K.; Du, J.; Ye, Q.H.; Cragg, G.M.; et al. Antineoplastic agents. 536. New sources of naturally occurring cancer cell growth inhibitors from marine organisms, terrestrial plants, and microorganisms(1a). J. Nat. Prod. 2008, 71, 438-444.
-
(2008)
J. Nat. Prod.
, vol.71
, pp. 438-444
-
-
Pettit, G.R.1
Hogan, F.2
Xu, J.P.3
Tan, R.4
Nogawa, T.5
Cichacz, Z.6
Pettit, R.K.7
Du, J.8
Ye, Q.H.9
Cragg, G.M.10
-
111
-
-
33750160748
-
Stereocontrolled total synthesis of bengazole A: A marine bisoxazole natural product displaying potent antifungal properties
-
DOI 10.1002/anie.200602050
-
Bull, J.A.; Balskus, E.P.; Horan, R.A.; Langner, M.; Ley, S.V. Stereocontrolled total synthesis of bengazole A: A marine bisoxazole natural product displaying potent antifungal properties. Angew. Chem. Int. Ed. 2006, 45, 6714-6718. (Pubitemid 44600451)
-
(2006)
Angewandte Chemie - International Edition
, vol.45
, Issue.40
, pp. 6714-6718
-
-
Bull, J.A.1
Balskus, E.P.2
Horan, R.A.J.3
Langner, M.4
Ley, S.V.5
-
112
-
-
0033603499
-
First total synthesis of bengazole A
-
Mulder, R.J.; Shafer, C.M.; Molinski, T.F. First total synthesis of bengazole A. J. Org. Chem. 1999, 64, 4995-4998.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 4995-4998
-
-
Mulder, R.J.1
Shafer, C.M.2
Molinski, T.F.3
-
113
-
-
65149091999
-
Synthesis and structure-activity relationships of bengazole A analogs
-
Mulder, R.J.; Shafer, C.M.; Dalisay, D.S.; Molinski, T.F. Synthesis and structure-activity relationships of bengazole A analogs. Bioorg. Med. Chem. Lett. 2009, 19, 2928-2930.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2928-2930
-
-
Mulder, R.J.1
Shafer, C.M.2
Dalisay, D.S.3
Molinski, T.F.4
-
114
-
-
0000747989
-
Reactions of lithiooxazole
-
Hodges, J.C.; Patt, W.C.; Connolly, C.J. Reactions of lithiooxazole. J. Org. Chem. 1991, 56, 449-452.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 449-452
-
-
Hodges, J.C.1
Patt, W.C.2
Connolly, C.J.3
-
115
-
-
0000858597
-
Metalation of oxazole-borane complexes: A practical solution to the problem of electrocyclic ring opening of 2-lithiooxazoles
-
Vedejs, E.; Monaham, S.D. Metalation of oxazole-borane complexes: A practical solution to the problem of electrocyclic ring opening of 2-lithiooxazoles. J. Org. Chem. 1996, 61, 5192-5193.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 5192-5193
-
-
Vedejs, E.1
Monaham, S.D.2
-
116
-
-
0032492936
-
Synthesis of the C1-C9 core of bengazole A: Harnessing the ambident nucleophilicity of 2-lithiooxazole
-
DOI 10.1016/S0040-4039(98)00494-8, PII S0040403998004948
-
Shafer, C.M.; Molinski, T.F. Synthesis of the C1-C9 core of bengazole A: Harnessing the ambident nucleophilicity of 2-lithiooxazole. Tetrahedron Lett. 1998, 39, 2903-2906. (Pubitemid 28184055)
-
(1998)
Tetrahedron Letters
, vol.39
, Issue.19
, pp. 2903-2906
-
-
Shafer, C.M.1
Molinski, T.F.2
-
117
-
-
0142020462
-
Synthetic studies on bengazoles of marine sponge origin. Synthesis of the core bis-oxazole fragments
-
Chittari, P.; Hamada, Y.; Shioiri, T. Synthetic studies on bengazoles of marine sponge origin. Synthesis of the core bis-oxazole fragments. Synlett 1998, 1022-1024. (Pubitemid 128693970)
-
(1998)
Synlett
, Issue.9
, pp. 1022-1024
-
-
Chittari, P.1
Hamada, Y.2
Shioiri, T.3
-
118
-
-
0037344397
-
A synthetic approach to bengazoles: A synthesis of deacylbengazole
-
Chittari, P.; Hamada, Y.; Shioiri, T. A synthetic approach to bengazoles: A synthesis of deacylbengazole. Heterocycles 2003, 59, 465-472.
-
(2003)
Heterocycles
, vol.59
, pp. 465-472
-
-
Chittari, P.1
Hamada, Y.2
Shioiri, T.3
-
119
-
-
84981911072
-
2-Unsubstituted oxazoles from alpha-metalated Isocyanides and acylating agents
-
Schöllkopf, U.; Schröder, R. 2-Unsubstituted oxazoles from alpha-metalated Isocyanides and acylating agents. Angew. Chem. Int. Ed. Engl. 1971, 10, 333.
-
(1971)
Angew. Chem. Int. Ed. Engl.
, vol.10
, pp. 333
-
-
Schöllkopf, U.1
Schröder, R.2
-
120
-
-
0029840044
-
Studies directed toward the synthesis of ulapualide A. Asymmetric synthesis of the C8-C25 tris-oxazole fragment
-
DOI 10.1021/jo960532r
-
Panek, J.S.; Beresis, R.T. Studies directed toward the synthesis of Ulapualide A. Asymmetric synthesis of the C8-C25 tris-oxazole fragment. J. Org. Chem. 1996, 61, 6496-6497. (Pubitemid 26328636)
-
(1996)
Journal of Organic Chemistry
, vol.61
, Issue.19
, pp. 6496-6497
-
-
Panek, J.S.1
Beresis, R.T.2
-
121
-
-
34547467756
-
Total synthesis of potent antifungal marine bisoxazole natural products bengazoles A and B
-
DOI 10.1002/chem.200700033
-
Bull, J.A.; Balskus, E.P.; Horan, R.A.; Langner, M.; Ley, S.V. Total synthesis of potent antifungal marine bisoxazole natural products bengazoles A and B. Chem. Eur. J. 2007, 13, 5515-5538. (Pubitemid 47160163)
-
(2007)
Chemistry - A European Journal
, vol.13
, Issue.19
, pp. 5515-5538
-
-
Bull, J.A.1
Balskus, E.P.2
Horan, R.A.J.3
Langner, M.4
Ley, S.V.5
-
122
-
-
74949139942
-
Total synthesis of bengazole A
-
Chandrasekhar, S.; Sudhakar, A. Total synthesis of bengazole A. Org. Lett. 2010, 12, 236-238.
-
(2010)
Org. Lett.
, vol.12
, pp. 236-238
-
-
Chandrasekhar, S.1
Sudhakar, A.2
-
123
-
-
0032489407
-
Diastereoselective synthesis of γ-hydroxy-β-amino alcohols and (2S,3S)-β-hydroxyleucine from chiral D-(N,N-dibenzylamino) serine (TBDMS) aldehyde
-
DOI 10.1021/jo971468w
-
Laïb, T.; Chastanet, J.; Zhu, J. Diastereoselective synthesis of γ-hydroxy-β-amino alcohols and (2S,3S)-β-hydroxyleucine from chiral D-(N,N-dibenzylamino)serine (TBDMS) aldehyde. J. Org. Chem. 1998, 63, 1709-1713. (Pubitemid 28136916)
-
(1998)
Journal of Organic Chemistry
, vol.63
, Issue.5
, pp. 1709-1713
-
-
Laib, T.1
Chastanet, J.2
Zhu, J.3
-
124
-
-
33846820522
-
A short alternative preparation of the bengazoles polyol side-chain segment
-
DOI 10.1016/j.carres.2006.12.020, PII S0008621506005799
-
Gallos, J.K.; Stathakis, C.I.; Salapassidou, M.J.; Grammatoglou, C.E.; Koumbis, A.E. A short alternative preparation of the bengazoles polyol side-chain segment. Carbohydr. Res. 2007, 342, 744-748. (Pubitemid 46204661)
-
(2007)
Carbohydrate Research
, vol.342
, Issue.5
, pp. 744-748
-
-
Gallos, J.K.1
Stathakis, C.I.2
Salapassidou, M.J.3
Grammatoglou, C.E.4
Koumbis, A.E.5
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