Licence: Public Domain Mark
Credit: Index-catalogue of medical and veterinary zoology. Source: Wellcome Collection.
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Nat, v. 71, 3.8., Dp. 63-122, illus., pls, [W2.] BARNER? [Dr.] : 1952 a.—Wurzelnematoden a] Raldrian <Nach- richtenbl. Deutsch. Pfianzenschutzdienst, v. $2, n. s., v. 6 (1), Jan. p. 15; illus. [W.] BAEZ, MANUEL MARTINEZ. See Martinez Baez, Manuel: BAHMANYAR, M.. Bahmanyar, M. BAILEY, WILFORD SHERRILL [D. V. M.., Se. D., Ala- bama: Polytech: Inst.] [See also. Folse, ‘Dean S.; and Bailey, Wilford Sherrill] 1953 a.—Lesions of.“ selected parasitic infec- tions <Vet.. Med. v. 48 (6), Gig pp. 238, Able yt Weel BAinEs, R.-C.;. CLARKE, O.-F.;.and pweia. WeP. 1948 ’a.—Susceptibility. of some citrus species and other piants to the citrus-roct nematode, Tylenchulus semipenetrans [Abstract of re- port. before 80. Ann.-Meéet.,. Pacific Div., Am. Phytopath... Soe.,- . Berkeley, ..June 22-25] <Phytopathology, v. 88 (11),. Now, Ds 912. [W2.] Seer aiknratd) Marcel; ‘and Bakr, A.D. {Nematode Lab., Div. Entom., Ot- tawa] 1952 a.—Notes on some nematode problems, 1951 <Canad. Insect. Pest Rev., v.80 (1), pp. 118-120. [W.] Baker, B. R.; et al. 1952 a—An antimalarial alkaloid from Hy- drangea. XIV. Synthesis of 5-, 6-, 7—, and 8-monosubstituted derivatives <J. Org. Chem., v. 17 (1), Jan., pp. 141-148. [W:.] 1952. b.—-An . antimalarial alkaloid from Hy- drangea. XV. Synthesis of 5-, 6-, 7-, and 8- derivatives with two identical substituents <J. Org. Chem., v. 17. (1), Jan, pp. 149- 156. [W8.] 1952 c.—An. antimalarial alkaloid from. Hy- drangea. XVI. Synthesis of 5-, 6-, 7-, and 8-derivatives with twe different substituents <J. Org. Chem., v. 17 (1), Jan., pp. 157- 163. [Wea.] 1952 d—-An gauibala Hal alkaloid Enotes Hy- drangea. VII. 8-[6- keto-y-(5=hydroxy—2- piperidyl) propyl]-4-quinazolone, an isomer <J. Org. Chem., v.17 (1), Jan., pp. 68-76. [We.] | 1952 e—An antimalarial alkaloid from’ Hy- drangea. XVII. Some 5-—substituted deriva- tives <J. “teh Chem:,:v. 17 = Jan., pp. 164-176. [Wa4.] BAKER, B. R.; QUERRY, MERLE V.; KapisH, Ar- THUR F.; ‘and WILLIAMS, JAMES H. 1952 a.—An antimalarial alkaloid from’ Hy- drangea. IV. Functional derivatives of 3- alkyl-4-quinazelones <J. Org. Chem:, v. 17 2 (1) »Jan., ppwd5-51:.. [We] 1852 b.—An antimalarial alkaloid from. Hy- drangea. V. Some 3—(4-keto-sec-aminoallky!) - pas vaer ee <i ei Chem., v. ET (1), pp. 52-57. -[W2.] © ERT B.; and WILLIAMS, JAMES H. 1952: a.—An antimalarial alkaloid from Hy- drangea. VI. <A second synthesis of 3-[8- keto-Y- (2-piperidyl)= - “propyi]-4-quinazolone <J./ Org. Chem., v: 17 (1), Jan., pp. 68-67. [we.] Baker, B. R.; ScHaus, RopertT E.; McEvoy, FRANCIS J.; and WILLIAMS, JAMES H. 1952°a.—An antimalarial alkaloid: from Hy- drangea. XII. synthesis of 8—[-f-keto-7- (hy- droxy-2-piperidyl) propyl]-4-quinazolone, the alkaloid <J. Org. Chem., v. 17 (1), Jan., pp. 182-140. [Ws.] Baker, B. R.; ScHaus, Ropert E.; QueErry, MEpRLE V.; and WILLIAMS, JAMES H. 1952 a—An antimalarial alkaloid from Hy- drangea. VIII... Attempted synthesis. of 3-[4- keto-7- (4-hydroxy-2- piperidy!)-4-quinazolone by the ba a ea approach <J. Org. Chem., v. 17 (1), Jan., pp. 77-96. [W2.] 1952. b.—An_ antimalarial alkaloid from Hy- _, drangea. IX. Synthesis, of 3-[?-keto-7- (4- hydroxy-2- piperidyl). _ propyl]-4-quinazolone, an isomer <J. Org. Chem,, v.17, (1), Jan., pp. 97-108. [W:] Baker, Bw R.; SCHAUB; ROBERT E: and WILLIAMs, JAMES H. : 1952 a.—An antimalarial alkaloid: from -Hy- drangea.’’ XX. Synthesis of 8-[*-keto-7-(4- methyl-2-pyrrolidyl) propyl! |-4-quinazolone _ ane Chem:, Vv. 17 (1), Jan., pp. 109-115. a&](https://iiif.wellcomecollection.org/image/b32181553_0008_0015.jp2/full/800%2C/0/default.jpg)
