| LDR | | 01798nmm uu200385 4500 |
| 001 | | 000000333529 |
| 005 | | 20240805173214 |
| 008 | | 181129s2018 |||||||||||||||||c||eng d |
| 020 | |
▼a 9780438009608 |
| 035 | |
▼a (MiAaPQ)AAI10817425 |
| 035 | |
▼a (MiAaPQ)grad.msu:16103 |
| 040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 248032 |
| 082 | 0 |
▼a 547 |
| 100 | 1 |
▼a Dai, Yijing. |
| 245 | 10 |
▼a Catalytic Asymmetric Multi-Component Kabachnik-Fields Reaction by Vanol-Derived Zirconium Complex and Total Synthesis of Sphingoid Bases. |
| 260 | |
▼a [S.l.] :
▼b Michigan State University.,
▼c 2018 |
| 260 | 1 |
▼a Ann Arbor :
▼b ProQuest Dissertations & Theses,
▼c 2018 |
| 300 | |
▼a 230 p. |
| 500 | |
▼a Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B. |
| 500 | |
▼a Adviser: William D. Wulff. |
| 502 | 1 |
▼a Thesis (Ph.D.)--Michigan State University, 2018. |
| 520 | |
▼a A highly efficient asymmetric catalytic approach to synthesize -amino phosphonates by employing aldehydes, amines and diethyl phosphites under a chiral VANOL-derived zirconium complex was developed. The asymmetric induction of this direct three- |
| 520 | |
▼a Sphingoid bases are backbones of new class sphingolipids and they have four different members present in two-headed family with similar structure, but with different stereochemistry. The key step in the synthesis of sphingoid bases are nucleophi |
| 590 | |
▼a School code: 0128. |
| 650 | 4 |
▼a Organic chemistry. |
| 690 | |
▼a 0490 |
| 710 | 20 |
▼a Michigan State University.
▼b Chemistry. |
| 773 | 0 |
▼t Dissertation Abstracts International
▼g 79-10B(E). |
| 773 | |
▼t Dissertation Abstract International |
| 790 | |
▼a 0128 |
| 791 | |
▼a Ph.D. |
| 792 | |
▼a 2018 |
| 793 | |
▼a English |
| 856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T14998363
▼n KERIS |
| 980 | |
▼a 201812
▼f 2019 |
| 990 | |
▼a 관리자 |