Chemistry of Heterocyclic Compounds: Pyridine and Its by R. A. Abramovitch PDF

February 27, 2018 | Systems Planning | By admin | 0 Comments

By R. A. Abramovitch

ISBN-10: 0470186690

ISBN-13: 9780470186695

ISBN-10: 0471379166

ISBN-13: 9780471379164

Content material:
Chapter XIII Pyridine Alcohols (pages 1–114): Ellis V. Brown
Chapter XIV Pyridine Aldehydes and Ketones (pages 115–187): Renat H. Mizzoni
Chapter XV Sulfur and Selenium Compounds of Pyridine (pages 189–443): Harry L. Yale
Chapter XVI Pyridines and diminished Pyridines of Pharmacological curiosity (pages 445–524): R. T. Coutts and A. F. Casy

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Extra resources for Chemistry of Heterocyclic Compounds: Pyridine and Its Derivatives, Supplement, Part Four, Volume 14

Example text

P. 175-176" 2-PyPhCHCOH(2-thienyl)CW(CH ), 2PyPhCHCOH(CH3 )CH(CH, 2-PyPhCHCOH(CH3)CH,Ph 2PyPhCHCOH(CH, )CH, CH, (3-indoyl) 2-PyCH, - 1cyclohexanol-2CH2OCH, Ref. Physical properties (derivatives) Compound TABLE XlII-12. P. P. P. p. r. p. p. p. p. p. 09 rnm;TNBS". p. p. p. p. p. p. 115-125"/9 mm; fl;? P. p. p. P. P. p. p. p. p. p. p. p. P. p. p. P. P. p. p. - 2-PyCHPhCOHCZH, (4C1C6 H,) "Trinitrobenzenesul fonate. p. p. p. p. p. p. p. p. p. p. p. p. p. 2380 2PyCH,CHOH(CH, CH, -2-Py) 2-PyCH,CH2CHOHCH2CHCH3NO, 2-Pycyclopropyl€OH(CR, =CH-CH, ), 2-PyCHOHC(CH3), 2-PyPhCOHCH(CH3), 2-PyPhCOHCH2CHaCH, 2-PyPhCOHC.

P. P. p. p. p. P. p. P. P. p. 1lo", 119-1 20" ;Lr. r. p. 1. p. r. p. p. r. p. r. p. p. r. p. p. p. p. r. p. p. p. 75-77"; HCI. ma. p. P. p. p. p. 50' (EtOH) 49 49 129 52 146 146 146 80 80 80 13,49 13 146 80 53 80 80 50 50,52 so Ref. p. p. V. p. V. p. p. V. p. p. V. p. p. p. V. p. p. V. p. p. V. p. p. V. p. p. v. p. p. V. p. p. V. p. p. V. p. p. V. p. p. V. p. p. V. p. p. v. p. 1. p. V. p. p. V. p. p. V. 4 OCH, CH, -2-Py 2-PyCH, CH, OCH, -_ Compound TABLE XIII-15. 40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 Ref.

P. r. p. p. r. p. r. p. p. r. p. p. p. p. r. p. p. p. 75-77"; HCI. ma. p. P. p. p. p. 50' (EtOH) 49 49 129 52 146 146 146 80 80 80 13,49 13 146 80 53 80 80 50 50,52 so Ref. p. p. V. p. V. p. p. V. p. p. V. p. p. p. V. p. p. V. p. p. V. p. p. V. p. p. v. p. p. V. p. p. V. p. p. V. p. p. V. p. p. V. p. p. V. p. p. v. p. 1. p. V. p. p. V. p. p. V. 4 OCH, CH, -2-Py 2-PyCH, CH, OCH, -_ Compound TABLE XIII-15. 40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 39,40,179 Ref.

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Chemistry of Heterocyclic Compounds: Pyridine and Its Derivatives, Supplement, Part Four, Volume 14 by R. A. Abramovitch


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