Citation: Dw. Ma et W. Zhu, Two-component method to enantiopure quinolizidinones and indolizidinones. Total synthesis of (-)-lasubine II, ORG LETT, 3(24), 2001, pp. 3927-3929
Citation: Dw. Ma et Cf. Xia, Cul-catalyzed coupling reaction of beta-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857, ORG LETT, 3(16), 2001, pp. 2583-2586
Citation: Dw. Ma et al., First total synthesis of martinellic acid, a naturally occurring bradykinin receptor antagonist, ORG LETT, 3(14), 2001, pp. 2189-2191
Citation: Dw. Ma et al., Synthesis of benzofuran analogue of Go6976, an isoform-selective protein kinase C inhibitor, CHIN J CHEM, 19(5), 2001, pp. 488-492
Citation: Y. Wang et Dw. Ma, Synthesis of enantiopure N-protected 4,5-disubstituted 3-pyrrolidinones and N-protected 2,5-disubstituted 3-pyrrolidinones via the Dieckmann reactionof dicarbonyl compounds derived from enantiopure beta-amino esters, TETRAHEDR-A, 12(5), 2001, pp. 725-730
Citation: Dw. Ma, Recent advances in the discovery of protein kinase C modulators based on the structures of natural protein kinase C activators, CURR MED CH, 8(2), 2001, pp. 191-202
Citation: Dw. Ma et al., Facile synthesis of (+)-alpha-allokainic acid via Pd-catalyzed hydrogenolysis of allyl acetate derived from trans-4-hydroxy-L-proline, TETRAHEDR L, 42(39), 2001, pp. 6929-6931
Citation: Dw. Ma et Qq. Wu, Synthesis of the biaryl moiety of the proteasome inhibitors TMC-95 via a ligandless Pd(OAc)(2)-catalyzed Suzuki-coupling reaction, TETRAHEDR L, 42(31), 2001, pp. 5279-5281
Citation: K. Ding et Dw. Ma, Asymmetric synthesis of alpha,alpha-disubstituted amino acids by diastereoselective functionalization of enantiopure phenyloxazinones, derivatives ofasymmetric Strecker reaction products of aldehydes, TETRAHEDRON, 57(30), 2001, pp. 6361-6366
Citation: Dw. Ma et Jd. Yang, Total synthesis of kaitocephalin, the first naturally occurring AMPA/KA receptor antagonist, J AM CHEM S, 123(39), 2001, pp. 9706-9707
Citation: Dw. Ma et Hy. Sun, A simple and stereospecfic route to 2,6-disubstituted 4-hydroxypiperidines. Synthesis of dendrobate alkaloid (+)-241D and formal synthesis of (-)-indolizidine 167B, ORG LETT, 2(16), 2000, pp. 2503-2505
Citation: Dw. Ma et K. Ding, Synthesis of enantiopure alpha,alpha-disubstituted amino acids from the asymmetric Strecker reaction products of aldehydes, ORG LETT, 2(16), 2000, pp. 2515-2517
Citation: B. Peng et al., Chiral guanidine catalyzed Michael addition reaction and Diels-Alder reaction of anthrone and N-methylmaleimide, CHIN J CHEM, 18(3), 2000, pp. 411-413
Citation: Dw. Ma et Qq. Wu, Enantioselective construction of the oxidized tryptophan fragment of proteasome inhibitors TMC-95A and TMC-95B, TETRAHEDR L, 41(47), 2000, pp. 9089-9093
Citation: Dw. Ma et al., Synthesis of (2S,1 ' R,2 ' R,3 ' R)-2-(2 ',3 '-dicarboxycyclopropyl)-glycine via the stereochemically controlled cyclopropanation of (S)-glyceraldehyde acetonide-derived enones, TETRAHEDRON, 56(38), 2000, pp. 7447-7456
Citation: Dw. Ma et Hy. Sun, General route to 2,4,5-trisubstituted piperidines from enantiopure beta-amino esters. Total synthesis of pseudodistomin B triacetate and pseudodistomin F, J ORG CHEM, 65(19), 2000, pp. 6009-6016
Citation: G. Chen et al., The fundamental solution for shallow circular cylindrical shells - Part I:derivations, INT J ENG S, 38(11), 2000, pp. 1235-1257
Citation: Dw. Ma et al., Stereochemically controlled cyclopropanation of (S)-glyceraldehyde acetonide-derived olefins. Synthesis of (2S,1 ' R,2 ' R,3 ' R)-2-(2 ',3 '-dicarboxycyclopropyl)glycine, ORG LETT, 1(2), 1999, pp. 285-287