Recent Developments on Carbon-Carbon Bond Forming Reactions in Water

被引:16
作者
Chaturvedi, Devdutt [1 ]
Barua, Nabin C. [1 ]
机构
[1] CSIR, NE Inst Sci & Technol, Nat Prod Chem Div, Jorhat 785006, Assam, India
关键词
Carbon-carbon bond forming reactions; green reaction media; water; SONOGASHIRA COUPLING REACTION; SUBSTITUTED PYRIDINES; OLEFIN-METATHESIS; ARYL BROMIDES; EFFICIENT SYNTHESIS; PALLADIUM ACETATE; ORGANIC-REACTIONS; ROOM-TEMPERATURE; SUZUKI REACTIONS; FACILE SYNTHESIS;
D O I
10.2174/157017912798889170
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In recent years water has emerged as a versatile solvent for the synthesis of a variety of organic compounds employing plethora of organic reactions. Water as a solvent is not only inexpensive and environmentally benign, but also exhibits new reactivity. The types of organic reactions in water are broad including pericyclic reactions, reactions of carbanion equivalents, reactions of carbocation equivalents, reactions of radicals and carbenes, transition metal catalysis, oxidations-reductions, etc. In the present review, we are focusing on some recent and most important carbon-carbon bond forming reactions utilizing water as a reaction media published from the year 2005 onwards.
引用
收藏
页码:17 / 30
页数:14
相关论文
共 104 条
[1]   An efficient conversion of conjugated oximes into substituted pyridines under Vilsmeier conditions [J].
Ahmed, S ;
Boruah, RC .
TETRAHEDRON LETTERS, 1996, 37 (45) :8231-8232
[2]  
Alickmann D, 2002, EUR J ORG CHEM, V2002, P1523
[3]   Synthesis of 3-aroylnicotinonitriles from aroylketene dithioacetals [J].
Anabha, E. R. ;
Nirmala, K. N. ;
Thomas, Abraham ;
Asokan, C. V. .
SYNTHESIS-STUTTGART, 2007, (03) :428-432
[4]   The tethered Biginelli condensation in natural product synthesis [J].
Aron, ZD ;
Overman, LE .
CHEMICAL COMMUNICATIONS, 2004, (03) :253-265
[5]   Microwave-promoted Suzuki coupling reactions with organotrifluoroborates in water using ultra-low catalyst loadings [J].
Arvela, RK ;
Leadbeater, NE ;
Mack, TL ;
Kormos, CM .
TETRAHEDRON LETTERS, 2006, 47 (02) :217-220
[6]   FURANNULATION STRATEGY FOR SYNTHESIS OF THE NATURALLY-OCCURRING FUSED 3-METHYLFURANS - EFFICIENT SYNTHESIS OF EVODONE AND MENTHOFURAN AND REGIOSELECTIVE SYNTHESIS OF MATURONE VIA A LEWIS-ACID CATALYZED DIELS-ALDER REACTION - SOME COMMENTS FOR ITS MECHANISTIC ASPECTS [J].
ASO, M ;
OJIDA, A ;
YANG, G ;
CHA, OJ ;
OSAWA, E ;
KANEMATSU, K .
JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (15) :3960-3968
[7]  
Atta-ur-Rahman, 1990, STUDIES NATURAL PROD, V6, P107
[8]   A modified and green methodology for preparation of polysubstituted furans [J].
Azizian, J ;
Mohammadizadeh, MR ;
Mohammadi, AA ;
Karimi, AR .
HETEROATOM CHEMISTRY, 2005, 16 (04) :259-262
[9]   Nickel-Catalyzed Alkynylation of Aryl Iodides (Sonogashira Reaction) in Water [J].
Bakherad, Mohammad ;
Keivanloo, Ali ;
Mihanparast, Samira .
SYNTHETIC COMMUNICATIONS, 2010, 40 (02) :179-185
[10]   Copper-free Sonogashira coupling reactions catalyzed by a water-soluble Pd-salen complex under aerobic conditions [J].
Bakherad, Mohammad ;
Keivanloo, Ali ;
Bahramian, Bahram ;
Hashemi, Mahdieh .
TETRAHEDRON LETTERS, 2009, 50 (14) :1557-1559