Jae Chol Lee

Total Synthesis of (−)-Colchicine by an Oxyallyl [4+3] Cycloaddition

Jae Chol Lee, Jin Kun · Tetrahedron · 2000 · 62 citations

Engineering, Bioorganic Chemistry, Total Synthesis +4

Total Synthesis of Colchicine. α-Methoxy-Substituted Oxyallyl [4 + 3] Cycloaddition Approach

Jae Chol Lee, Shujuan Jin, Jin Kun · The Journal of Organic Chemistry · 1998 · 61 citations

Bioorganic Chemistry, Engineering, Biochemistry +12

Diastereoselective Synthesis of trans-1,2-Dialkylcyclopropanols by the Kulinkovich Hydroxycyclopropanation of Homoallylic Alcohols This work was supported by the National Institutes of Health (GM35956) and National Science Foundation (CHE98-13975).

Long Guo Quan, Seho Kim, Jae Chol Lee et al. · Angewandte Chemie International Edition · 2002 · 61 citations

Kulinkovich Hydroxycyclopropanation, Engineering, Heterocyclic +12

Total Synthesis of Tropoloisoquinolines:  Imerubrine, Isoimerubrine, and Grandirubrine¹

Jae Chol Lee, Jin Kun · Journal of the American Chemical Society · 2001 · 59 citations

Diastereoselective synthesis of trans-1,2-dialkylcyclopropanols by the Kulinkovich hydroxycyclopropanation of homoallylic alcohols.

Long Guo Quan, Se-Ho Kim, Jae Chol Lee et al. · PubMed · 2002 · 53 citations

Kulinkovich Hydroxycyclopropanation, Engineering, Diastereoselective Synthesis +6