서울대학교 중앙도서관
S-Space 소개
My S-Space
로그인이 필요합니다.
Login

S-Space

Browse

Subject

Jump to a point in the index
Or type in a year

  • Sort by
  • In order
  • Results/Page
  • Authors/record

Showing results 1 to 9 of 9

Issue DateTitle / Author(s) / CitationFileAltmetrics
1994-05
Activation of the Maillard Reaction Product 5-(Hydroxymethyl)furfural to Strong Mutagens via Allylic Sulfonation and Chlorination

Surh, Young-Joon; Tannenbaum, Steven R.

Chemical Research in Toxicology, Vol.7 No.3, pp.313-318

DOI
2011-12
Highly enantioselective phase‐transfer catalytic α‐alkylation of α‐tert‐butoxycarbonyllactams: Construction of β‐quaternary chiral pyrrolidine and piperidine systems
DOI
2013-06
Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates

Ha, Min Woo; Hong, Suckchang; Park, Cheonhyoung; Park, Yohan; Lee, Jihye; Kim, Mi-Hyun; Lee, Jihoon; Park, Hyeung-Geun

Organic and Biomolecular Chemistry, Vol.11 No.24, pp.4030-4039

DOI
2014-03
Enantioselective synthesis of α-halo-α-alkylmalonates via phase-transfer catalytic α-alkylation
DOI
2014-10
Asymmetric synthesis and evaluation of α-quaternary chiral lactam derivatives as novel anticancer agents

Lee, Hwanhyuk; Hwang, Su Jung; Jung, Jisung; Hong, Suckchang; Lee, Myungmo; Park, Hyeung-geun; Lee, Hyo-Jong; Park, Yohan

Archives of Pharmacal Research, Vol.37 No.10, pp.1264-1270

DOI
2015-09
Enantioselective α-alkylation of benzylideneamino tert-butyl malonates by phase-transfer catalysis
DOI
2016-08
Phase-transfer catalyzed enantioselective α-alkylation of α-acyloxymalonates: construction of chiral α-hydroxy quaternary stereogenic centers
DOI
2017-05
Enantioselective synthesis of chiral α-azido and α-aryloxy quaternary stereogenic centers via the phase-transfer-catalyzed α-alkylation of α-bromomalonates, followed by SN2 substitution

Kim, Doyoung; Ha, Min Woo; Hong, Suck Chang; Park, Cheonhyoung; Kim, Byungsoo; Yang, Jewon; Park, Hyeung-Geun

Journal of Organic Chemistry, Vol.82 No.9, pp.4936-4943

DOI
2023-08
Targeted and Logical Discovery of Piperazic Acid-Bearing Natural Products Based on Genomic and Spectroscopic Signatures
DOI
1