Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
February 16, 2001Angewandte Chemie

Geminal Difunctionalization of Alkenylidene-Type Carbenoids by Using Interelement Compounds

View Full Paper
Ask AI
Bookmark
Share

Authors

THTakeshi HataKanazawa UniversityHKHirotaka KitagawaNagoya Institute of TechnologyHMHirokazu MasaiNational Institute of Advanced Industrial Science and Technology

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Hata et al. (2001) studied this question.

synapsesocial.com/papers/6aa4db856803e1e7a1f2dc7ahttps://doi.org/10.1002/1521-3757(20010216)113:4<812::aid-ange8120>3.0.co;2-o
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Reactions of cis- and trans-1,4-dichloro-2-butene with sodium amide1968 · 12 citations
  2. 2Nucleophilic addition reactions of hindered unsaturated boranes. New synthesis of organoboranes1987 · 48 citations
  3. 3Vinylic organoboranes. 6. A general synthesis of (E)-disubstituted-alkenes or ketones via the (E)-(1-substituted-1-alkenyl)boronic esters1986 · 34 citations
  4. 4Migratory insertion reactions of organometallics. 3. Carbon-carbon bond forming reactions of organotransition metals with .alpha.- or .gamma.-haloorganolithium reagents1989 · 95 citations
  5. 5Zinc and copper carbenoids as efficient and selective a1/d1 multicoupling reagents. 11989 · 82 citations