-
2
-
-
0002944551
-
The chemistry and biochemistry of simple indolizidine and related polyhydroxy alkaloids
-
In: Pelletier S W, ed, New York: Wiley, 1987. Chapter 1
-
Molyneux R J, Elbein A D. The chemistry and biochemistry of simple indolizidine and related polyhydroxy alkaloids. In: Pelletier S W, ed. Alkaloids: Chemical and Biological Perspective. New York: Wiley, 1987. Chapter 1.
-
Alkaloids: Chemical and Biological Perspective
-
-
Molyneux, R.J.1
Elbein, A.D.2
-
4
-
-
36749025633
-
Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
-
Galliford C V, Scheidt K A. Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents. Angew Chem Int Ed, 2007, 46: 8748-8758.
-
(2007)
Angew Chem Int Ed
, vol.46
, pp. 8748-8758
-
-
Galliford, C.V.1
Scheidt, K.A.2
-
5
-
-
40849130719
-
A facile and efficient synthesis of highly functionalised 3,3′-dispiropyrrolidine- and 3,3′-dispiropyrrolizidine bisoxindoles via [3+2] cycloaddition
-
Shanmugam P, Viswambharan B, Selvakumar K, et al. A facile and efficient synthesis of highly functionalised 3, 3′-dispiropyrrolidine- and 3, 3′-dispiropyrrolizidine bisoxindoles via [3+2] cycloaddition. Tetrahedron Lett, 2008, 49: 2611-2615.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 2611-2615
-
-
Shanmugam, P.1
Viswambharan, B.2
Selvakumar, K.3
-
6
-
-
0020686579
-
Potential anticonvulsant. VI: Condensation of isatins with cyclohexanone and other cyclic ketones
-
Pajouhesh H, Parsons R, Popp F D. Potential anticonvulsant. VI: Condensation of isatins with cyclohexanone and other cyclic ketones. J Pharm Sci, 1983, 72: 318-321.
-
(1983)
J Pharm Sci
, vol.72
, pp. 318-321
-
-
Pajouhesh, H.1
Parsons, R.2
Popp, F.D.3
-
7
-
-
33746297623
-
Highly diastereoselective one-pot synthesis of spirocyclic oxindoles through intramolecular Ullmann coupling and Claisen rearrangement
-
Miyamoto H, Okawa Y, Nakazaki A, et al. Highly diastereoselective one-pot synthesis of spirocyclic oxindoles through intramolecular Ullmann coupling and Claisen rearrangement. Angew Chem Int Ed, 2006, 45: 2274-2277.
-
(2006)
Angew Chem Int Ed
, vol.45
, pp. 2274-2277
-
-
Miyamoto, H.1
Okawa, Y.2
Nakazaki, A.3
-
8
-
-
0038392407
-
Recent applications to the synthesis of oxindole alkaloids
-
Marti C, Carreira E M. Recent applications to the synthesis of oxindole alkaloids. Eur J Org Chem, 2003, 2209-2219.
-
(2003)
Eur J Org Chem
, pp. 2209-2219
-
-
Marti, C.1
Carreira, E.M.2
-
9
-
-
0031689165
-
Recent progress in the chemistry of non-monoterpenoid indole alkaloids
-
Toyota M, Ihara M. Recent progress in the chemistry of non-monoterpenoid indole alkaloids. Nat Prod Rep, 1998, 15: 327-340.
-
(1998)
Nat Prod Rep
, vol.15
, pp. 327-340
-
-
Toyota, M.1
Ihara, M.2
-
10
-
-
0038287938
-
Enantioselective synthesis of 3-alkyl-3-aryl-oxindoles by catalytic asymmetric intramolecular Heck reactions
-
Dounary A B, Hatanaka K, Kodanko J J, et al. Enantioselective synthesis of 3-alkyl-3-aryl-oxindoles by catalytic asymmetric intramolecular Heck reactions. J Am Chem Soc, 2003, 125: 6261-6271.
-
(2003)
J Am Chem Soc
, vol.125
, pp. 6261-6271
-
-
Dounary, A.B.1
Hatanaka, K.2
Kodanko, J.J.3
-
11
-
-
0035905004
-
Corrigendum to Novel indole-type glucosinolates from woad (Isatis tinctoria L.)
-
Frechard A, Fabre N, Pean C, et al. Corrigendum to "Novel indole-type glucosinolates from woad (Isatis tinctoria L.)". Tetrahedron Lett, 2001, 42: 9015-9017.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 9015-9017
-
-
Frechard, A.1
Fabre, N.2
Pean, C.3
-
12
-
-
0035132521
-
Maremycins C and D, new diketopiperazines, and maremycins E and F, novel polycyclic spiro-indole metabolites isolated from streptomyces sp
-
Tang Y Q, Sattler I, Thiericke R, et al. Maremycins C and D, new diketopiperazines, and maremycins E and F, novel polycyclic spiro-indole metabolites isolated from streptomyces sp. Eur J Org Chem, 2001, 261-267.
-
(2001)
Eur J Org Chem
, pp. 261-267
-
-
Tang, Y.Q.1
Sattler, I.2
Thiericke, R.3
-
13
-
-
77954317442
-
Asymmetric addition of indoles to isatins catalyzed by bifunctional modified cinchona alkaloid catalysts
-
Chauhan P, Chimni S S. Asymmetric addition of indoles to isatins catalyzed by bifunctional modified cinchona alkaloid catalysts. Chem Eur J, 2010, 16: 7709-7713.
-
(2010)
Chem Eur J
, vol.16
, pp. 7709-7713
-
-
Chauhan, P.1
Chimni, S.S.2
-
14
-
-
39349095269
-
Supramolecular synthesis of 3-indolyl-3-hydroxy oxindoles under neutral conditions in water
-
Kumar V P, Reddy V P, Sridhar R, et al. Supramolecular synthesis of 3-indolyl-3-hydroxy oxindoles under neutral conditions in water. J Org Chem, 2008, 73: 1646-1648.
-
(2008)
J Org Chem
, vol.73
, pp. 1646-1648
-
-
Kumar, V.P.1
Reddy, V.P.2
Sridhar, R.3
-
15
-
-
77349115131
-
Synthesis of symmetrical and unsymmetrical 3,3′-di(indolyl)indolin-2-ones under controlled catalysis of ionic liquids
-
Rad-Moghadam K, Sharifi-Kiasaraie M, Taheri-Amlashi H. Synthesis of symmetrical and unsymmetrical 3, 3′-di(indolyl)indolin-2-ones under controlled catalysis of ionic liquids. Tetrahedron, 2010, 66: 2316-2321.
-
(2010)
Tetrahedron
, vol.66
, pp. 2316-2321
-
-
Rad-Moghadam, K.1
Sharifi-Kiasaraie, M.2
Taheri-Amlashi, H.3
-
16
-
-
79954421874
-
New four-component reactions in water: A convergent approach to the metal-free synthsis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4-b]pyridine] derivatives
-
Balamurugan K, Perumal S, Menéndez J C. New four-component reactions in water: A convergent approach to the metal-free synthsis of spiro[indoline/acenaphthylene-3, 4′-pyrazolo[3, 4-b]pyridine] derivatives. Tetrahedron, 2011, 67: 3201-3208.
-
(2011)
Tetrahedron
, vol.67
, pp. 3201-3208
-
-
Balamurugan, K.1
Perumal, S.2
Menéndez, J.C.3
-
17
-
-
0036069165
-
Interaction of izatins with some five-membered aminoheterocycles
-
Pushechnikov A O, Volochnyuk D M, Tolmachev A A. Interaction of izatins with some five-membered aminoheterocycles. Synlett, 2002, 1140-1142.
-
(2002)
Synlett
, pp. 1140-1142
-
-
Pushechnikov, A.O.1
Volochnyuk, D.M.2
Tolmachev, A.A.3
-
18
-
-
77954559449
-
Efficient one-pot synthesis of novel spirooxindole derivatives via three-component reaction in aqueous medium
-
Chen H, Shi D Q. Efficient one-pot synthesis of novel spirooxindole derivatives via three-component reaction in aqueous medium. J Comb Chem, 2010, 12: 571-576.
-
(2010)
J Comb Chem
, vol.12
, pp. 571-576
-
-
Chen, H.1
Shi, D.Q.2
|