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Items: 1 to 20 of 114

1.

Synthesis of 1-(4-trifluoromethoxyphenyl)-2,5-dimethyl-3-(2-R-thiazol-4-yl)-1H-pyrroles via chain heterocyclization.

Vovk MV, Pinchuk OM, Tolmachov AO, Gakh AA.

Molecules. 2010 Feb 23;15(2):997-1006. doi: 10.3390/molecules15020997.

2.

Carbon-carbon bond formation and pyrrole synthesis via the [3,3] sigmatropic rearrangement of O-vinyl oxime ethers.

Wang HY, Mueller DS, Sachwani RM, Londino HN, Anderson LL.

Org Lett. 2010 May 21;12(10):2290-3. doi: 10.1021/ol100659q.

PMID:
20411970
3.

Regioselective synthesis of 2,3,4- or 2,3,5-trisubstituted pyrroles via [3,3] or [1,3] rearrangements of O-vinyl oximes.

Wang HY, Mueller DS, Sachwani RM, Kapadia R, Londino HN, Anderson LL.

J Org Chem. 2011 May 6;76(9):3203-21. doi: 10.1021/jo200061b. Epub 2011 Mar 30.

PMID:
21449572
4.

A novel one-pot pyrrole synthesis via a coupling-isomerization-Stetter-Paal-Knorr sequence.

Braun RU, Zeitler K, Müller TJ.

Org Lett. 2001 Oct 18;3(21):3297-300.

PMID:
11594818
5.

A new facile approach to the synthesis of 3-methylthio-substituted furans, pyrroles, thiophenes, and related derivatives.

Yin G, Wang Z, Chen A, Gao M, Wu A, Pan Y.

J Org Chem. 2008 May 2;73(9):3377-83. doi: 10.1021/jo702585s. Epub 2008 Mar 20.

PMID:
18351746
6.

A general route to 1,3'-bipyrroles.

Cheng P, Shao W, Clive DL.

J Org Chem. 2013 Dec 6;78(23):11860-73. doi: 10.1021/jo401892t. Epub 2013 Nov 26.

PMID:
24251686
7.

Transition metal mediated construction of pyrrole ring on 2,3-dihydroquinolin-4(1H)-one: synthesis and pharmacological evaluation of novel tricyclic heteroarenes.

Layek M, Reddy M A, Rao AV, Alvala M, Arunasree MK, Islam A, Mukkanti K, Iqbal J, Pal M.

Org Biomol Chem. 2011 Feb 21;9(4):1004-7. doi: 10.1039/c0ob00771d. Epub 2010 Dec 23.

PMID:
21180745
8.

Modular one-pot synthesis of tetrasubstituted pyrroles from alpha-(alkylideneamino)nitriles.

Bergner I, Opatz T.

J Org Chem. 2007 Sep 14;72(19):7083-90. Epub 2007 Aug 22.

PMID:
17713947
9.

Solution phase synthesis of a library of tetrasubstituted pyrrole amides.

Bianchi I, Forlani R, Minetto G, Peretto I, Regalia N, Taddei M, Raveglia LF.

J Comb Chem. 2006 Jul-Aug;8(4):491-9.

PMID:
16827560
10.

Simple synthesis of substituted pyrroles.

Banik BK, Samajdar S, Banik I.

J Org Chem. 2004 Jan 9;69(1):213-6.

PMID:
14703403
11.

Intermediates in the Paal-Knorr synthesis of pyrroles. 4-Oxoaldehydes.

Amarnath V, Amarnath K, Valentine WM, Eng MA, Graham DG.

Chem Res Toxicol. 1995 Mar;8(2):234-8.

PMID:
7766806
12.

Furan ring opening-pyrrole ring closure: a new synthetic route to aryl(heteroaryl)-annulated pyrrolo[1,2-a][1,4]diazepines.

Butin AV, Nevolina TA, Shcherbinin VA, Trushkov IV, Cheshkov DA, Krapivin GD.

Org Biomol Chem. 2010 Jul 21;8(14):3316-27. doi: 10.1039/c002994g. Epub 2010 Jun 4.

PMID:
20523958
13.

Synthesis of functionalized tetrahydro-1,3-diazepin-2-ones and 1-carbamoyl-1H-pyrroles via ring expansion and ring expansion/ring contraction of tetrahydropyrimidines.

Fesenko AA, Trafimova LA, Shutalev AD.

Org Biomol Chem. 2012 Jan 14;10(2):447-62. doi: 10.1039/c1ob06284k. Epub 2011 Nov 15.

PMID:
22083389
14.

Flow synthesis using gaseous ammonia in a Teflon AF-2400 tube-in-tube reactor: Paal-Knorr pyrrole formation and gas concentration measurement by inline flow titration.

Cranwell PB, O'Brien M, Browne DL, Koos P, Polyzos A, Peña-López M, Ley SV.

Org Biomol Chem. 2012 Aug 14;10(30):5774-9. doi: 10.1039/c2ob25407g. Epub 2012 Apr 24.

PMID:
22532036
15.

Solution-phase synthesis of a tricyclic pyrrole-2-carboxamide discovery library applying a stetter-Paal-Knorr reaction sequence.

Werner S, Iyer PS, Fodor MD, Coleman CM, Twining LA, Mitasev B, Brummond KM.

J Comb Chem. 2006 May-Jun;8(3):368-80.

16.

Design and synthesis of pyrrolotriazepine derivatives: an experimental and computational study.

Menges N, Sari O, Abdullayev Y, Erdem SS, Balci M.

J Org Chem. 2013 Jun 7;78(11):5184-95. doi: 10.1021/jo4001228. Epub 2013 May 21.

PMID:
23647431
17.

Highly stereoselective and scalable synthesis of trans-fused octahydrocyclohepta[b]pyrrol-4(1H)-ones via the aza-Cope-Mannich rearrangement in racemic and enantiopure forms.

Belov DS, Lukyanenko ER, Kurkin AV, Yurovskaya MA.

J Org Chem. 2012 Nov 16;77(22):10125-34. doi: 10.1021/jo301762a. Epub 2012 Nov 6.

PMID:
23113580
18.

Highly regioselective synthesis of 3,4-disubstituted 1H-pyrrole.

Liu JH, Chan HW, Wong HN.

J Org Chem. 2000 Jun 2;65(11):3274-83.

PMID:
10843606
19.

Ultrasound-assisted synthesis of 2,5-dimethyl-N-substituted pyrroles catalyzed by uranyl nitrate hexahydrate.

Satyanarayana VS, Sivakumar A.

Ultrason Sonochem. 2011 Sep;18(5):917-22. doi: 10.1016/j.ultsonch.2011.02.007. Epub 2011 Mar 17.

PMID:
21419686
20.

Early amidation approach to 3-[(4-amido)pyrrol-2-yl]-2-indolinones.

Manley JM, Kalman MJ, Conway BG, Ball CC, Havens JL, Vaidyanathan R.

J Org Chem. 2003 Aug 8;68(16):6447-50.

PMID:
12895087

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